This document summarizes molecular basis of mutations. It defines mutations as changes in genetic information and describes different types of mutations including point mutations, chromosomal mutations, germline mutations and somatic mutations. It also discusses various mutagens responsible for mutations like chemical mutagens such as alkylating agents, base analogs and reactive oxygen species, and physical mutagens like UV radiation and ionizing radiation. The mechanisms of different mutagens and types of mutations based on their phenotypic effects are also summarized.
C VALUE, C VALUE PARADOX , COT CURVE ANALYSIS.pptxMurugaveni B
This document discusses the C-value, C-value paradox, and COT curve analysis. It defines the C-value as the total amount of DNA in a genome. It explains that the C-value paradox arose because early research assumed complexity increased with DNA amount, but some organisms like salamanders have more DNA than humans despite lower complexity. The document outlines the COT curve technique which analyzes renaturation kinetics to measure genome complexity based on repetitive sequences. It applies COT curve analysis to understand genome size, sequence complexity, and the proportion of single-copy versus repetitive DNA.
1. There are two main methods of gene transfer - direct and indirect gene transfer. Indirect transfer uses Agrobacterium-mediated transformation while direct transfer uses physical or chemical methods.
2. Agrobacterium-mediated transformation uses Agrobacterium tumefaciens to transfer T-DNA containing the gene of interest into the plant genome. The process involves co-cultivation of plant explants with Agrobacterium followed by selection and regeneration of transgenic plants.
3. Direct physical methods include biolistic transformation, microinjection, electroporation, and macroinjection. Direct chemical methods include PEG-mediated, calcium phosphate co-precipitation, and liposome-mediated transformation
This document discusses several key concepts related to gene structure:
1. Genes in eukaryotes contain both coding (exon) and non-coding (intron) sequences. Introns are removed during RNA processing to form mRNA.
2. Benzer performed fine structure analysis of phage T4 genes which demonstrated that genes can undergo intragenic recombination, or crossing over within the gene. This established that genes have an internal structure smaller than previously believed.
3. Split genes were discovered, which have interrupted sequences (introns) between coding sequences (exons). RNA splicing removes introns to form mature mRNA from split genes.
This document discusses cytoplasmic male sterility (CMS), a maternally inherited trait in plants where the plant is unable to produce functional pollen. CMS is caused by mitochondrial mutations or rearrangements that interfere with pollen development. Nuclear restorer genes can suppress CMS by interacting with the mitochondrial genes. CMS is used in hybrid seed production systems in many crops.
Electroporation is a method to transform cells by creating transient pores in the cell membrane through applying brief high-voltage electric pulses, allowing DNA to enter the cell. It involves suspending cells in a solution with DNA between electrodes and applying pulses of 4000-8000 V/cm for milliseconds. This forms pores in the membrane through which DNA can enter. It is commonly used to transform bacteria, yeast, plant protoplasts, and transfect eukaryotic cells. Key factors influencing electroporation include field strength, pulse length, DNA purity and concentration, and cell growth conditions.
The document summarizes key information about Ti plasmids, which are plasmids found in Agrobacterium tumefaciens that cause crown gall disease in plants. The Ti plasmid transfers a segment of DNA called T-DNA into the host plant genome, integrating genes that cause tumor formation. The plasmid has regions for T-DNA, virulence genes needed for transfer, and sometimes opine catabolism genes. Ti plasmids are used to create transgenic plants by replacing the tumor genes with a gene of interest in the T-DNA.
This document summarizes molecular basis of mutations. It defines mutations as changes in genetic information and describes different types of mutations including point mutations, chromosomal mutations, germline mutations and somatic mutations. It also discusses various mutagens responsible for mutations like chemical mutagens such as alkylating agents, base analogs and reactive oxygen species, and physical mutagens like UV radiation and ionizing radiation. The mechanisms of different mutagens and types of mutations based on their phenotypic effects are also summarized.
C VALUE, C VALUE PARADOX , COT CURVE ANALYSIS.pptxMurugaveni B
This document discusses the C-value, C-value paradox, and COT curve analysis. It defines the C-value as the total amount of DNA in a genome. It explains that the C-value paradox arose because early research assumed complexity increased with DNA amount, but some organisms like salamanders have more DNA than humans despite lower complexity. The document outlines the COT curve technique which analyzes renaturation kinetics to measure genome complexity based on repetitive sequences. It applies COT curve analysis to understand genome size, sequence complexity, and the proportion of single-copy versus repetitive DNA.
1. There are two main methods of gene transfer - direct and indirect gene transfer. Indirect transfer uses Agrobacterium-mediated transformation while direct transfer uses physical or chemical methods.
2. Agrobacterium-mediated transformation uses Agrobacterium tumefaciens to transfer T-DNA containing the gene of interest into the plant genome. The process involves co-cultivation of plant explants with Agrobacterium followed by selection and regeneration of transgenic plants.
3. Direct physical methods include biolistic transformation, microinjection, electroporation, and macroinjection. Direct chemical methods include PEG-mediated, calcium phosphate co-precipitation, and liposome-mediated transformation
This document discusses several key concepts related to gene structure:
1. Genes in eukaryotes contain both coding (exon) and non-coding (intron) sequences. Introns are removed during RNA processing to form mRNA.
2. Benzer performed fine structure analysis of phage T4 genes which demonstrated that genes can undergo intragenic recombination, or crossing over within the gene. This established that genes have an internal structure smaller than previously believed.
3. Split genes were discovered, which have interrupted sequences (introns) between coding sequences (exons). RNA splicing removes introns to form mature mRNA from split genes.
This document discusses cytoplasmic male sterility (CMS), a maternally inherited trait in plants where the plant is unable to produce functional pollen. CMS is caused by mitochondrial mutations or rearrangements that interfere with pollen development. Nuclear restorer genes can suppress CMS by interacting with the mitochondrial genes. CMS is used in hybrid seed production systems in many crops.
Electroporation is a method to transform cells by creating transient pores in the cell membrane through applying brief high-voltage electric pulses, allowing DNA to enter the cell. It involves suspending cells in a solution with DNA between electrodes and applying pulses of 4000-8000 V/cm for milliseconds. This forms pores in the membrane through which DNA can enter. It is commonly used to transform bacteria, yeast, plant protoplasts, and transfect eukaryotic cells. Key factors influencing electroporation include field strength, pulse length, DNA purity and concentration, and cell growth conditions.
The document summarizes key information about Ti plasmids, which are plasmids found in Agrobacterium tumefaciens that cause crown gall disease in plants. The Ti plasmid transfers a segment of DNA called T-DNA into the host plant genome, integrating genes that cause tumor formation. The plasmid has regions for T-DNA, virulence genes needed for transfer, and sometimes opine catabolism genes. Ti plasmids are used to create transgenic plants by replacing the tumor genes with a gene of interest in the T-DNA.
This document discusses inheritance and provides examples of cytoplasmic inheritance. It describes Mendelian inheritance where genes located on chromosomes segregate in predictable ratios. Non-Mendelian inheritance involves genes located in the cytoplasm that are transmitted from the female parent only, with no segregation in F2 generations. Examples discussed include chloroplast inheritance in Mirabilis jalapa, kappa particles determining toxicity in Paramoecium, and shell coiling determined by cytoplasmic proteins in snails. Cytoplasmic male sterility is also summarized, where mitochondrial mutations cause pollen to be non-functional but are maternally inherited.
This document summarizes information about Arabidopsis thaliana, a small flowering plant that is widely used as a model organism. It describes A. thaliana's physical characteristics and life cycle, genome, and use in understanding flower development. Specifically, it outlines the ABC model of flower development in which three classes of genes (A, B, and C) interact to specify the four types of floral organs - sepals, petals, stamens, and carpels. Mutations in these genes result in homeotic transformations where one organ develops in place of another.
This document discusses numerical chromosomal aberrations. It defines euploidy as having an exact multiple of the haploid chromosome number, and aneuploidy as having more or less than the euploid number. The main types of euploidy are monoploidy, diploidy, and polyploidy. Polyploidy can be autopolyploidy, with identical chromosome sets, or allopolyploidy involving chromosomes from different species. Aneuploidy includes hypoploidy, with fewer chromosomes, and hyperploidy, with extras. Specific aneuploid conditions discussed are monosomy, nullisomy, trisomy, and tetrasomy.
Recombination model and cytological basis of crossing overAlex Harley
This study evaluated the effect of expressing multiple heterologous recombinases on increasing homologous recombination in tobacco plants. The recombinases RecA, RecG, RuvC, Rad51, Rad52 and DMC1 were expressed individually and in combinations in tobacco plants containing a recombination substrate. Expression of DMC1 alone produced the greatest stimulation of homologous recombination, increasing recombination frequency up to 1000-fold. Expression of other recombinases also increased recombination 2 to 380-fold. Increasing homologous recombination could improve the efficiency of gene targeting for plant biotechnology applications using CRISPR/Cas.
The document discusses selectable marker genes that are commonly used in plant transformation systems. Selectable marker genes are included in transformation vectors along with the target gene of interest. They confer resistance to transformed cells when grown on media containing toxic substances like antibiotics, herbicides, or antimetabolites. This allows transformed cells to survive while non-transformed cells die. There are three main categories of selectable marker genes: antibiotic resistance genes, antimetabolite marker genes, and herbicide resistance genes. Common examples of genes used include nptII for kanamycin resistance, pat/bar for phosphinothricin/glufosinate resistance, and epsps/aroA for glyphosate resistance.
This document discusses several topics in biochemical genetics:
1. Phenylketonuria is caused by a mutation that prevents the enzyme phenylalanine hydroxylase from functioning properly, causing phenylalanine to build up.
2. Alkaptonuria is a rare genetic disorder caused by mutations in the HGD gene, which prevents breakdown of phenylalanine and tyrosine. It causes darkening of the urine, joints, and other tissues over time.
3. Beadle and Tatum studied the biochemical pathway of arginine in Neurospora and found evidence supporting the one gene-one enzyme hypothesis, where each step in a metabolic pathway is controlled by a specific enzyme from a
The brief note on B-Chromosomes with characteristics and research case studies.
This particular studies has more scope for further experimental evidences.
Transposons are segments of DNA that can change position within a genome, causing mutations. There are two types: DNA transposons, which move directly between positions, and retrotransposons, which are transcribed to RNA and then reverse transcribed to DNA before inserting elsewhere. Transposons move via either a "cut and paste" mechanism or a "copy and paste" mechanism. They have been useful research tools for mutagenesis and studying gene expression, but can also cause genetic diseases.
Retrotransposons are genetic elements that copy and paste themselves throughout the genome using an RNA intermediate and reverse transcription. There are two main types: LTR retrotransposons, which mimic retroviruses through reverse transcription of an RNA copy into DNA; and non-LTR retrotransposons like LINEs and SINEs. LINEs (Long Interspersed Nuclear Elements) are autonomous retrotransposons over 6kb with endonuclease and reverse transcriptase proteins. SINEs (Short Interspersed Nuclear Elements) are shorter than 300bp and non-autonomous, relying on LINEs to reverse transcribe themselves.
Gene tagging uses recognizable DNA fragments like T-DNA or transposons to disrupt gene function and identify genes responsible for mutant phenotypes. T-DNA tagging in plants involves random integration of Agrobacterium T-DNA that can disrupt genes and create mutants. Transposon tagging relies on the ability of transposons to move within genomes and disrupt gene function. Both techniques have been used successfully to isolate numerous plant genes involved in traits like color and development.
Transportable elements are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are also known as “Jumping genes”.
This document discusses different concepts of genes including classical concepts like alleles and modern concepts like jumping genes, overlapping genes, split genes, nested genes, and fusion genes. It then focuses on jumping genes or transposons, providing details on their discovery by Barbara McClintock in maize in the 1940s. Transposons are able to move from one location in the chromosome to another. The document discusses types of transposons like IS-elements, P-elements, and retrotransposons. It also discusses the significance of transposons and examples of transposon systems in maize like the Ac-Ds system.
ANEUPLOIDY (Introduction, classification, merits and demerits)Bushra Hafeez
Aneuploidy is a type of chromosomal abnormality in which numbers of chromosomes are abnormal.Generally, the aneuploid chromosome set differs from wild type by only one or a small number of chromosomes. It is a genetic disorder causes birth defects. It is the second major category of chromosome mutations in which chromosome number is abnormal.
Aneuploid nomenclature is based on the number of copies of the specific chromosome in the aneuploid state. For example, the aneuploid condition 2n − 1 is called monosomic (meaning “one chromosome”) because only one copy of some specific chromosome is present instead of the usual two found in its diploid progenitor. The aneuploid 2n + 1 is called trisomic,2n − 2 is nullisomic, and n + 1 is disomic.
This document discusses yeast artificial chromosomes (YACs) and bacterial artificial chromosomes (BACs). YACs are engineered chromosomes derived from yeast DNA that can clone very large DNA sequences in yeast cells of up to 1 megabase. BACs are cloning vectors derived from bacterial DNA that can clone DNA fragments of up to 300 kilobases in E. coli. Both systems allow cloning and propagation of large DNA fragments, but YACs can hold more DNA while BACs are more stable and better for functional analysis in mammalian cells.
Somatic cell hybridization involves fusing cells from two different species, such as human and mouse cells, to form hybrid cells containing chromosomes from both species. This technique allows genes to be mapped to specific chromosomes. It works by using selective growth conditions that require the hybrid cell to retain certain human chromosomes in order to survive. Over successive cell divisions, human chromosomes are eliminated at random except for those required for survival. This allows the creation of cell lines containing partial sets of human chromosomes that can be analyzed to correlate genes with specific chromosomes. The technique has been important for mapping the human genome.
The document summarizes a case study where the whole genomes of six gamma-irradiated rice plants were sequenced to identify mutations induced by radiation exposure. High-quality sequencing data was obtained and analyzed to detect single nucleotide substitutions, short insertions/deletions, and structural variations compared to the reference genome. The identified mutations were further validated using PCR analysis. The study demonstrates how whole genome sequencing can be used to characterize mutations induced in plants by gamma radiation exposure.
Dr.S.KARTHIKUMAR
Associate Professor
Department of Biotechnology
Kamaraj College of Engineering and Technology, K.Vellakulam-625701, TN, India
Email: skarthikumar@gmail.com
Gene cloning involves copying a gene and inserting it into a self-replicating vector to produce multiple copies of the gene. PCR (polymerase chain reaction) is a technique used to amplify specific genes. Both gene cloning and PCR are important for obtaining pure samples of genes and amplifying them for various applications like sequencing, expression of proteins, and genetic engineering.
Basic principle of gene expression & methods ofshrikant wankhede
This document discusses gene expression and methods of gene transfer. It begins by defining gene expression as the process by which information from a gene is used to produce a functional product, often a protein. It then explains the central dogma of biology - that DNA is transcribed into RNA which is translated into protein. The document focuses on viral and non-viral methods of gene transfer, describing several types of viral vectors including retroviruses, lentiviruses, adenoviruses, and adeno-associated viruses. It also discusses non-viral methods such as electroporation, gene guns, oligonucleotides, and liposomes. Finally, it briefly mentions some applications of gene transfer technologies.
Transgenic plants are plants that have been genetically modified to express desirable traits. Genes can be transferred from one plant species to another using Agrobacterium tumefaciens, a soil bacterium. Agrobacterium transfers DNA from its tumor-inducing (Ti) plasmid into the plant genome. The Ti plasmid contains genes that cause tumors as well as a region that can be replaced with a gene of interest. Transformed plants are regenerated and screened for the introduced trait. Common traits introduced include herbicide and insect resistance, improved nutrition, and environmental stress tolerance.
Introduction
Definition
History
Why are the transgenic animals being produced
Transgenic mice
Mice: as model organism
Methods of creation of transgenic mice
knock-out mice
Application of transgenic mice
Conclusion
References
Transgenic animals are produced by introducing foreign DNA into an animal's genome. The first transgenic animal was a mouse created in 1974. Since then, various methods have been used to generate transgenic fish, livestock, and other species. Transgenic animals have applications in biomedical research, agriculture, and industry. They can serve as models for human disease or help produce pharmaceuticals in their milk. However, transgenesis also carries risks if the inserted gene has unintended effects on the animal's development or physiology.
This document discusses inheritance and provides examples of cytoplasmic inheritance. It describes Mendelian inheritance where genes located on chromosomes segregate in predictable ratios. Non-Mendelian inheritance involves genes located in the cytoplasm that are transmitted from the female parent only, with no segregation in F2 generations. Examples discussed include chloroplast inheritance in Mirabilis jalapa, kappa particles determining toxicity in Paramoecium, and shell coiling determined by cytoplasmic proteins in snails. Cytoplasmic male sterility is also summarized, where mitochondrial mutations cause pollen to be non-functional but are maternally inherited.
This document summarizes information about Arabidopsis thaliana, a small flowering plant that is widely used as a model organism. It describes A. thaliana's physical characteristics and life cycle, genome, and use in understanding flower development. Specifically, it outlines the ABC model of flower development in which three classes of genes (A, B, and C) interact to specify the four types of floral organs - sepals, petals, stamens, and carpels. Mutations in these genes result in homeotic transformations where one organ develops in place of another.
This document discusses numerical chromosomal aberrations. It defines euploidy as having an exact multiple of the haploid chromosome number, and aneuploidy as having more or less than the euploid number. The main types of euploidy are monoploidy, diploidy, and polyploidy. Polyploidy can be autopolyploidy, with identical chromosome sets, or allopolyploidy involving chromosomes from different species. Aneuploidy includes hypoploidy, with fewer chromosomes, and hyperploidy, with extras. Specific aneuploid conditions discussed are monosomy, nullisomy, trisomy, and tetrasomy.
Recombination model and cytological basis of crossing overAlex Harley
This study evaluated the effect of expressing multiple heterologous recombinases on increasing homologous recombination in tobacco plants. The recombinases RecA, RecG, RuvC, Rad51, Rad52 and DMC1 were expressed individually and in combinations in tobacco plants containing a recombination substrate. Expression of DMC1 alone produced the greatest stimulation of homologous recombination, increasing recombination frequency up to 1000-fold. Expression of other recombinases also increased recombination 2 to 380-fold. Increasing homologous recombination could improve the efficiency of gene targeting for plant biotechnology applications using CRISPR/Cas.
The document discusses selectable marker genes that are commonly used in plant transformation systems. Selectable marker genes are included in transformation vectors along with the target gene of interest. They confer resistance to transformed cells when grown on media containing toxic substances like antibiotics, herbicides, or antimetabolites. This allows transformed cells to survive while non-transformed cells die. There are three main categories of selectable marker genes: antibiotic resistance genes, antimetabolite marker genes, and herbicide resistance genes. Common examples of genes used include nptII for kanamycin resistance, pat/bar for phosphinothricin/glufosinate resistance, and epsps/aroA for glyphosate resistance.
This document discusses several topics in biochemical genetics:
1. Phenylketonuria is caused by a mutation that prevents the enzyme phenylalanine hydroxylase from functioning properly, causing phenylalanine to build up.
2. Alkaptonuria is a rare genetic disorder caused by mutations in the HGD gene, which prevents breakdown of phenylalanine and tyrosine. It causes darkening of the urine, joints, and other tissues over time.
3. Beadle and Tatum studied the biochemical pathway of arginine in Neurospora and found evidence supporting the one gene-one enzyme hypothesis, where each step in a metabolic pathway is controlled by a specific enzyme from a
The brief note on B-Chromosomes with characteristics and research case studies.
This particular studies has more scope for further experimental evidences.
Transposons are segments of DNA that can change position within a genome, causing mutations. There are two types: DNA transposons, which move directly between positions, and retrotransposons, which are transcribed to RNA and then reverse transcribed to DNA before inserting elsewhere. Transposons move via either a "cut and paste" mechanism or a "copy and paste" mechanism. They have been useful research tools for mutagenesis and studying gene expression, but can also cause genetic diseases.
Retrotransposons are genetic elements that copy and paste themselves throughout the genome using an RNA intermediate and reverse transcription. There are two main types: LTR retrotransposons, which mimic retroviruses through reverse transcription of an RNA copy into DNA; and non-LTR retrotransposons like LINEs and SINEs. LINEs (Long Interspersed Nuclear Elements) are autonomous retrotransposons over 6kb with endonuclease and reverse transcriptase proteins. SINEs (Short Interspersed Nuclear Elements) are shorter than 300bp and non-autonomous, relying on LINEs to reverse transcribe themselves.
Gene tagging uses recognizable DNA fragments like T-DNA or transposons to disrupt gene function and identify genes responsible for mutant phenotypes. T-DNA tagging in plants involves random integration of Agrobacterium T-DNA that can disrupt genes and create mutants. Transposon tagging relies on the ability of transposons to move within genomes and disrupt gene function. Both techniques have been used successfully to isolate numerous plant genes involved in traits like color and development.
Transportable elements are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are also known as “Jumping genes”.
This document discusses different concepts of genes including classical concepts like alleles and modern concepts like jumping genes, overlapping genes, split genes, nested genes, and fusion genes. It then focuses on jumping genes or transposons, providing details on their discovery by Barbara McClintock in maize in the 1940s. Transposons are able to move from one location in the chromosome to another. The document discusses types of transposons like IS-elements, P-elements, and retrotransposons. It also discusses the significance of transposons and examples of transposon systems in maize like the Ac-Ds system.
ANEUPLOIDY (Introduction, classification, merits and demerits)Bushra Hafeez
Aneuploidy is a type of chromosomal abnormality in which numbers of chromosomes are abnormal.Generally, the aneuploid chromosome set differs from wild type by only one or a small number of chromosomes. It is a genetic disorder causes birth defects. It is the second major category of chromosome mutations in which chromosome number is abnormal.
Aneuploid nomenclature is based on the number of copies of the specific chromosome in the aneuploid state. For example, the aneuploid condition 2n − 1 is called monosomic (meaning “one chromosome”) because only one copy of some specific chromosome is present instead of the usual two found in its diploid progenitor. The aneuploid 2n + 1 is called trisomic,2n − 2 is nullisomic, and n + 1 is disomic.
This document discusses yeast artificial chromosomes (YACs) and bacterial artificial chromosomes (BACs). YACs are engineered chromosomes derived from yeast DNA that can clone very large DNA sequences in yeast cells of up to 1 megabase. BACs are cloning vectors derived from bacterial DNA that can clone DNA fragments of up to 300 kilobases in E. coli. Both systems allow cloning and propagation of large DNA fragments, but YACs can hold more DNA while BACs are more stable and better for functional analysis in mammalian cells.
Somatic cell hybridization involves fusing cells from two different species, such as human and mouse cells, to form hybrid cells containing chromosomes from both species. This technique allows genes to be mapped to specific chromosomes. It works by using selective growth conditions that require the hybrid cell to retain certain human chromosomes in order to survive. Over successive cell divisions, human chromosomes are eliminated at random except for those required for survival. This allows the creation of cell lines containing partial sets of human chromosomes that can be analyzed to correlate genes with specific chromosomes. The technique has been important for mapping the human genome.
The document summarizes a case study where the whole genomes of six gamma-irradiated rice plants were sequenced to identify mutations induced by radiation exposure. High-quality sequencing data was obtained and analyzed to detect single nucleotide substitutions, short insertions/deletions, and structural variations compared to the reference genome. The identified mutations were further validated using PCR analysis. The study demonstrates how whole genome sequencing can be used to characterize mutations induced in plants by gamma radiation exposure.
Dr.S.KARTHIKUMAR
Associate Professor
Department of Biotechnology
Kamaraj College of Engineering and Technology, K.Vellakulam-625701, TN, India
Email: skarthikumar@gmail.com
Gene cloning involves copying a gene and inserting it into a self-replicating vector to produce multiple copies of the gene. PCR (polymerase chain reaction) is a technique used to amplify specific genes. Both gene cloning and PCR are important for obtaining pure samples of genes and amplifying them for various applications like sequencing, expression of proteins, and genetic engineering.
Basic principle of gene expression & methods ofshrikant wankhede
This document discusses gene expression and methods of gene transfer. It begins by defining gene expression as the process by which information from a gene is used to produce a functional product, often a protein. It then explains the central dogma of biology - that DNA is transcribed into RNA which is translated into protein. The document focuses on viral and non-viral methods of gene transfer, describing several types of viral vectors including retroviruses, lentiviruses, adenoviruses, and adeno-associated viruses. It also discusses non-viral methods such as electroporation, gene guns, oligonucleotides, and liposomes. Finally, it briefly mentions some applications of gene transfer technologies.
Transgenic plants are plants that have been genetically modified to express desirable traits. Genes can be transferred from one plant species to another using Agrobacterium tumefaciens, a soil bacterium. Agrobacterium transfers DNA from its tumor-inducing (Ti) plasmid into the plant genome. The Ti plasmid contains genes that cause tumors as well as a region that can be replaced with a gene of interest. Transformed plants are regenerated and screened for the introduced trait. Common traits introduced include herbicide and insect resistance, improved nutrition, and environmental stress tolerance.
Introduction
Definition
History
Why are the transgenic animals being produced
Transgenic mice
Mice: as model organism
Methods of creation of transgenic mice
knock-out mice
Application of transgenic mice
Conclusion
References
Transgenic animals are produced by introducing foreign DNA into an animal's genome. The first transgenic animal was a mouse created in 1974. Since then, various methods have been used to generate transgenic fish, livestock, and other species. Transgenic animals have applications in biomedical research, agriculture, and industry. They can serve as models for human disease or help produce pharmaceuticals in their milk. However, transgenesis also carries risks if the inserted gene has unintended effects on the animal's development or physiology.
Principal of genetic engineering & its applications laraib jameel
Genetic engineering has many applications in medicine, including producing insulin, human growth hormones, vaccines, and monoclonal antibodies to treat diseases. It is also used to create animal models of human diseases and potentially cure conditions through gene therapy or stem cell therapy. For example, genetically modified bacteria are used to mass produce human insulin for diabetes treatment. Researchers are also working on genetically engineering foods to contain vaccines to more easily deliver them in developing countries.
Transgenic animals are created through genetic engineering by introducing foreign genes into the animal's genome. This allows the animal to produce proteins it would not normally make. Methods for creating transgenic animals include microinjection of DNA into fertilized eggs or embryonic stem cells. Transgenic animals have various applications including serving as disease models, producing pharmaceuticals in their milk (transpharmers), providing organs or tissues for transplantation (xenotransplantation), and enhancing food production. However, transgenic animal research also raises ethical issues regarding animal welfare and the environmental impacts of genetic modification.
Transgenic organisms and methods of their production.Garima
This document provides an overview of transgenic organisms. It begins with definitions of key terms like transgene, genome, plasmid, and restriction enzyme. It then discusses the history of transgenic research, including the first genetically modified organism created in 1973 and the first transgenic animals. The main methods used to produce transgenic animals are described as DNA microinjection, embryonic stem cell-mediated gene transfer, and retrovirus-mediated gene transfer. Current applications of transgenic organisms are outlined, such as glowing fish and insects used for pest control. The document concludes by discussing the importance of transgenic organisms in medicine, agriculture, and industry.
Transgenic animals are organisms that have been genetically engineered to carry foreign DNA in their genome. This document discusses transgenic animals, including their definition, goals, benefits and risks, types, methods of production, and applications. Some key points covered are: transgenic animals are useful for studying gene function and producing human proteins; common types include mice, fish, cows, and pigs; methods to create them include pronuclear microinjection and using embryonic stem cells or retroviruses; they have applications in research, agriculture, and biotechnology.
Transgenic animals are organisms whose genome has been altered by the addition of foreign DNA from other species. This document discusses the history of transgenic animals, including the first transgenic mice created in the 1970s. It describes various methods used to create transgenic animals, such as microinjection and viral vectors. The benefits and risks of transgenic animals are outlined. Applications include producing human proteins and studying human diseases. While transgenic animals show promise for agriculture, medicine, and industry, issues around safety, ethics, and environmental impacts require further consideration.
M.Sc; Transgenic mice as a model of human diseases.pptxSiddharthaSarkar49
Transgenic mice are commonly used as models for human diseases. Mice share many genetic and biological similarities with humans and can be genetically engineered to model specific human diseases and conditions. Transgenic technology allows foreign DNA to be introduced into mice to study the effects of certain genes and their role in various diseases like cancer, heart disease, and neurodegenerative disorders. Genetically engineered mouse models are valuable for understanding disease pathogenesis and identifying new diagnostic or therapeutic approaches. They provide insights that cannot be gained through cell or tissue studies alone.
This presentation gives a comprehensive detail of transgenic animal, processes involve in the production of transgenic animal and also highlights several benefits of transgenic animal
This document provides an overview of genetically modified animals. It begins with an introduction that defines genetically modified animals and notes that most are still in the research stage. It then discusses the process of genetic modification, which involves altering an animal's DNA in a way that does not occur naturally. The document outlines the process of creating genetically modified mammals through gene insertion and screening offspring. It provides examples of genetically modified pigs, cows, goats, mice, sheep, and chickens. The advantages include faster growth, disease resistance, and improved nutrition. Disadvantages include unintended harm, mutations, expense, and complex natural interactions.
Transgenic Animals developement and uses(M.NAGAPRADHEESH).pptxMNAGAPRADHEESH
DEVELOPEMENT AND USES OF TRANSGENIC ANIMALS:
■Definitions about Transgenic Animals (or) Genetically Modified Animals(GMO).
■History and Developements of Transgenic Animals(Yearwise:1907-2017)
■Different Methods used for developement of Transgenic animals:
1.Microinjection Method
2.Retro Viral Method
3.Embryonic Stem cell method
■Applications of Transgenic Animals
■Advantages of Transgenic Animals
■Disadvantages of Transgenic Animals
■References.
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Transgenic animals are created through recombinant DNA technology by inserting foreign genes into the animal's genome. This is done to improve livestock, use animals as bioreactors for pharmaceutical production, and for research purposes. The main methods of creating transgenic animals are DNA microinjection, retrovirus-mediated gene transfer, embryonic stem cell transfer, and sperm-mediated gene transfer. Examples include transgenic cows that produce more nutritious milk, pigs with genes to reduce environmental pollution, and mice used widely as model organisms. While transgenic animals have benefits, there are also ethical concerns regarding animal welfare and unintended environmental impacts.
This document summarizes the benefits of transgenic animals. It discusses how transgenic animals can be engineered through gene insertion to have desired traits. This technology has potential applications in agriculture by creating livestock with increased wool/milk production; in medicine by developing cows' milk that contains insulin or other proteins; and in industry by producing goats' milk containing spider silk proteins. While promising, the document notes there are also ethical concerns regarding animal welfare and unintended environmental impacts to consider.
Transgenic animals are animals whose DNA has been modified by the addition of foreign genes. Common transgenic animals include goats, mice, rabbits, sheep, dogs, and monkeys. Transgenic goats have been used to produce human proteins like antithrombin and alpha-fetoprotein in their milk. Methods for creating transgenic goats include somatic cell nuclear transfer and pronuclear microinjection. Transgenic mice and rabbits are also important research models, with mice commonly used to study gene function and model human diseases, while rabbits can produce human proteins and antibodies for therapeutic purposes. Transgenic animals have applications in pharmaceuticals, agriculture, biotechnology, and research.
This is about methods of creating transgenic animals,applications of transgenic animals in biotechnology and application of transgenic animals in pharmaceuticals.
Transgenic animals are animals that have been genetically modified to carry foreign genes inserted into their genome. This document discusses the production of transgenic animals, their applications in medicine, agriculture and industry, as well as issues related to their use. Transgenic animals are produced using techniques like pronuclear microinjection, retrovirus-mediated gene transfer, and embryonic stem cell-mediated gene transfer. They can be used for research, increasing agricultural yields, producing pharmaceuticals, and testing chemicals. However, there are also biosafety, ethical and environmental issues to consider with transgenic animals. With proper research and regulation, transgenic animals could help address problems that currently lack solutions.
Introduction
History
Landmarks Events in Transgenic Livestock Research
Techniques/ Method for Gene Transfer
Examples of transgenesis
Importance
Application
Limitation
Issue related to Transgenic Technology
Ethical concerns and how to Overcome
Transgenic manipulation of animal embryos and its applicationDeveshMachhi
INTRODUCTION
Genetic manipulation in animal for higher productivity is also called genetic engineering, refer to the alteration of the gene of an organism.
Organisms containing integrated sequences of cloned dna (transgenes), transferred using techniques of genetic engineering (to include those of gene transfer and gene substitution) are called transgenic animals.
Transgenic technology has led to the development of fishes, live stock and other animals with altered genetic profiles which are useful to mankind.Genetically modified animals are proving ever more vital in the development of new treatments and cures for many serious diseases.
Transgenesis is a radically new technology for altering the characteristics of animals by introducing the foreign genetic material.
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Transgenic animals are produced by inserting foreign DNA into the genome of an animal. The first transgenic animals were mice created in 1974 by injecting foreign DNA into mouse embryos. The presentation discusses the history of transgenic animals and the process used to produce them, including microinjection of DNA into fertilized eggs and using retroviruses. Advantages include improved traits for research, agriculture, and producing human proteins. Concerns include potential human health impacts and effects on the environment.
This presentation aims to provide an in-depth understanding of the science behind creating transgenic animals, explore their potential applications, and delve into the ethical considerations surrounding this emerging field of research.
Definition and Background:
We begin by defining transgenic animals as organisms that have had their genetic material intentionally altered through the introduction of foreign genes. This groundbreaking field of genetic engineering has its roots in the development of recombinant DNA technology in the 1970s, which enabled the transfer of genes across different species.
Genetic Engineering Techniques:
This section delves into the techniques employed to create transgenic animals, emphasizing the following key methodologies:
a. DNA Microinjection: The introduction of foreign DNA into the pronucleus of a fertilized embryo, allowing the foreign gene to be incorporated into the animal's genome and expressed in its cells.
b. Gene Targeting: The precise modification of an organism's genome by replacing or disrupting specific genes using technologies such as homologous recombination or CRISPR-Cas9.
c. Somatic Cell Nuclear Transfer (SCNT): The cloning technique involving the transfer of a nucleus from a somatic cell into an enucleated egg, resulting in the creation of an embryo with the same genetic makeup as the somatic cell donor.
Applications of Transgenic Animals:
This section explores the wide-ranging applications of transgenic animals across various fields, including:
a. Biomedical Research: Transgenic animals serve as invaluable models for studying human diseases and testing potential therapies, enabling significant advancements in medical research.
b. Agriculture: Transgenic animals can be engineered to possess desirable traits, such as increased resistance to diseases or improved meat quality, offering the potential to enhance agricultural productivity and sustainability.
c. Pharmaceutical Production: Transgenic animals can be designed to produce therapeutic proteins or antibodies in their milk or blood, providing a cost-effective means of manufacturing valuable pharmaceutical products.
d. Organ Transplantation: Research on transgenic animals has explored the possibility of generating organs that are genetically compatible with humans, addressing the shortage of donor organs for transplantation.
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APPLICATIONS OF GM ANIMALS...........pptx
1. APPLICATIONS
OF GM ANIMALS
Submitted by,
Adhithya Madhavan K S
Roll no :2
M.Sc. Botany
Submitted to,
Dr . Liza Jacob
Associate professor
Department of Botany
2. What are Transgenic Animals?
• Transgenic animals are the animals with the modified genome.
• A foreign gene is inserted into the genome of the animal to alter its DNA.
• This method is done to improve the genetic traits of the target animal.
• The foreign gene that is introduced is known as the transgene, and the
animal whose genome is altered is known as transgenic.
• These genes are passed on to the successive generations.
3. • The transgenic animals are genetically engineered and are
also known as genetically modified organisms (GMO)
• The first genetically modified organism was engineered in
the year 1980.
• Pigs, chickens, cows, fish, and mosquitoes are some of the
genetically modified animals produced by scientist
• In these animals, the embryo is genetically altered by the
gene of interest, and the resulting animal produces more
milk and meat, prevents diseases, etc.
4. Methods for Creating Transgenic
Animals
Physical Transfection
• In this method, the gene of interest is directly injected
into the pronucleus of a fertilized ovum.
• It is the very first method that proved to be effective in
mammals.
• This method was applicable to a wide variety of
species.
• Other methods of physical transfection include
particle bombardment, ultrasound and electroporation.
5. Chemical Transfection
• One of the chemical methods of gene transfection includes transformation.
• In this method, the target DNA is taken up in the presence of calcium phosphate.
• The DNA and calcium phosphate co-precipitates, which facilitates DNA uptake.
• The mammalian cells possess the ability to take up foreign DNA from the
culture medium.
6. Retrovirus-Mediated Gene Transfer
• To increase the chances of expression, the gene is transferred by means of a
vector.
• Since retroviruses have the ability to infect the host cell, they are used as
vectors to transfect the gene of interest into the target genome.
Viral Vectors
• Viruses are used to transfect rDNA into the animal cell. The viruses possess
the ability to infect the host cell, express well and replicate efficiently.
7. Examples of Transgenic Animals
Dolly Sheep
• Dolly the sheep was the first mammal to be cloned from an adult
cell.
• In this, the udder cells from a 6-year-old Finn Dorset white
sheep were injected into an unfertilized egg from a Scottish
Blackface ewe, which had its nucleus removed.
• The cell was made to fuse by electrical pulses.
• After the fusion of the nucleus of the cell with the egg, the
resultant embryo was cultured for six to seven days.
• It was then implanted into another Scottish Blackface ewe which
gave birth to the transgenic sheep, Dolly.
8. Transgenic Mice
• Transgenic mice are developed by injecting DNA into the oocytes or 1-2
celled embryos taken from female mice.
• After injecting the DNA, the embryo is implanted into the uterus of receptive
females.
9. APPLICATIONS OF GM ANIMALS
IN BASIC RESEARCH
• Genetically modified (GM) animals have a wide range of applications in
basic research, enabling scientists to study various biological
processes, diseases, and developmental mechanisms in ways that
were not possible before.
• Disease Modelling
• Gene Function Studies
• Developmental Biology
10. Disease Modeling:
• GM animals can be engineered to mimic human diseases, allowing researchers to
study disease progression, develop treatments, and understand underlying
mechanisms.
• For example, mice can be modified to develop symptoms similar to Parkinson's
disease, Alzheimer's disease, cancer, diabetes, and many other conditions.
• These models help researchers understand the genetic basis of diseases and test
potential therapies.
11. Gene Function Studies:
• By creating animals with specific genes knocked out (gene knockout) or
overexpressed (gene overexpression), scientists can determine the functions of
these genes in vivo.
• This approach is particularly useful for studying genes with unknown functions or
those implicated in diseases.
• For instance, researchers can create knockout mice lacking a particular gene to
observe the effects on development, behavior, or physiology.
12. Developmental Biology:
• GM animals are valuable tools for studying embryonic development and
organogenesis.
• By manipulating gene expression during embryonic development,
researchers can investigate the roles of specific genes in the formation of
tissues and organs.
• This research provides insights into normal development as well as the
causes of developmental disorders.
13. IN PRODUCING NOVEL PROTEIN
Transgenic animals were initially recognized as a novel platform for the
production of recombinant drug products for a number of reasons:
• It was demonstrated that transgenic approaches could reliably and safely
express novel proteins due to the unique nature of the mammary gland’s
capacity for production of complex molecules.
• Ability to produce significantly greater amounts of protein with higher
expression levels and volume output than the traditional protein culture
systems
14. • Transgenics demonstrated the potential for a significant reduction in the cost per
unit protein due to the animal being the true “bioreactor,” requiring less
complicated monitoring and industrial hardware than a traditional recombinant
cell culture system
• Genetically engineered animals held out the possibility of developing safer and
more sustainable and flexible manufacturing sources for vital human protein
replacements and blood products.
15. FOR DISEASE STUDIES
• The recent sequencing of the human and mouse genomes has revealed
remarkable similarities.
• Ninety-nine percent of the genes in these two genomes have direct counterparts
in the two species, although they have slightly different structures and functions.
• Because of this, the mouse is used as a model for research on human diseases.
• In GM models, detailed analyses of the development, physiology and
biochemistry of a particular disease can be related to a specific gene or group of
gene.
16. • It then becomes possible to understand the often complex relationship
between the gene and the disease process.
• The animals that are used most frequently to model the genetics of human
disease are the mouse, rat and zebrafish
17. Disease models in the mouse
• Gene dysfunction is at the root of all genetically determined disease processes.
• Checking how often mouse mutants reproduce the effect of mutations in the
corresponding human gene, it is possible to assess the utility and relevance of
disease models.
1) Diabetes:
• Mutations in the glucokinase gene in humans lead to a form of type II diabetes.
• Mutations in the glucokinase gene in the mouse also develop a type II diabetes,
very similar to that seen in humans.
• These mutants provide a useful model to investigate the relationship between
mutations in the glucokinase gene and the pathogenesis and severity of the
disease
18. 2) Human Immunodeficiency Virus/ Acquired Immunodeficiency Syndrome:
• Tg26 HIVAN Mouse Model was the first transgenic model developed in 1991 for
HIV.
• These transgenic animals can express HIV-1 proteins; develop symptoms and
immune deficiencies similar to the manifestations of AIDS in humans.
3) Cancer diseases:
• Oncomouse was first transgenic animal to be patented.
• Its germ cells and somatic cells contain an activated human oncogene sequence
introduced into the animal at an early embryonic stage to ensure that the oncogene
is present in all the animal cells.
19. For prevention and cure diseases
• Genetically modified (GM) animals hold significant potential for the prevention of
diseases through various approaches, including vaccine production, disease-
resistant animals, and gene editing technologies.
• Vaccine Production:
• GM animals can be engineered to produce vaccines against specific diseases.
• For example, researchers can introduce genes encoding antigens from pathogens
into the genome of animals such as goats, chickens, or pigs.
20. • These animals then produce the antigens in their milk, eggs, or blood, which can
be collected and used to manufacture vaccines.
• GM animals can be designed to produce edible vaccines
• the antigen is expressed in an edible part of the plant or animal, offering a
convenient and needle-free vaccination method.
• For example, measles vaccine is grown in chick embryo cells and polio vaccines
are grown in a mouse cell line.
• Another animal cell line, now being used to make egg-free flu vaccine, was
derived in 1958 from the kidney of a cocker spaniel.
21. Disease-Resistant Animals:
• Through genetic engineering, animals can be made resistant to specific
diseases.
• For example, pigs have been genetically modified to be resistant to porcine
reproductive and respiratory syndrome virus (PRRSV), a highly contagious and
economically significant disease in the swine industry.
• Disease-resistant GM animals also have implications for human health by
reducing the risk of zoonotic diseases, which can transmit from animals to
humans.
22. Gene Editing Technologies:
• gene editing technologies, such as CRISPR-Cas9, have revolutionized the field of
genetic engineering and opened up new possibilities for disease prevention in
animals.
• CRISPR-based techniques allow precise modification of the animal genome to
introduce or remove specific genes associated with disease susceptibility.
• For example, researchers have used CRISPR-Cas9 to create mosquitoes resistant
to malaria by altering genes involved in the parasite's lifecycle or in the mosquito's
immune response.