The Hardy- Weinberg principal is one of the recommended attributes used to calculate the gene frequency by scientists.
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The document provides information and instructions for an upcoming exam. It advises students to arrive early to review and relax, as arriving even a minute late could result in a zero grade. All personal items must be placed at the front of the room, and only a pencil and eraser are allowed during the exam. Use of any electronic devices will result in a zero. Students must write their name on the exam paper and Scantron, and bring a photo ID and student number to turn in the materials. Answer keys will be posted after the exam without photos allowed. Grades will be posted as soon as possible. Cheating is strictly prohibited.
The document provides an overview of the reproductive systems of vertebrates. It describes the general structures and functions of the male and female reproductive systems. Key points include: 1) The female system produces eggs and houses the embryo, while the male system produces sperm. 2) Structures such as ovaries, oviducts, uterus, and vagina are present across vertebrate classes with some variations. 3) Testes, ducts and accessory glands are the main male structures. 4) Fertilization and copulation methods vary between external in frogs to internal in mammals. 5) The cloaca is modified in different groups, remaining primitive in some and separating functions in others like mammals.
Polytene chromosomes are large chromosomes formed through repeated DNA replication without cell division in specialized cells like the salivary glands of Drosophila melanogaster. This process produces many sister chromatids that remain attached, increasing cell volume. Polytene chromosomes were first observed in insect larvae and are characterized by distinctive light and dark banding patterns that can be used to identify genetic changes. They provide benefits like high gene expression levels and have been useful for studying chromatin structure and genomic equivalence in organisms.
DNA barcoding uses a short, standardized gene sequence from a uniform region of mitochondrial or nuclear DNA to identify species. It has potential to identify the estimated 10 million eukaryotic species on Earth. The cytochrome c oxidase I (COI) gene region is commonly used for animals. DNA barcoding can identify specimens at all life stages, resolve taxonomic ambiguities, and enable development of electronic field guides. It involves tissue sampling, DNA extraction and amplification, sequencing, and comparing sequences to reference databases. Costs and time for the process are decreasing with new technologies. Global efforts aim to compile barcodes for all known eukaryotes.
Gene mapping | Genetic map | Physical Map | DNA Data Analysis (upgraded)NARC, Islamabad
Genes are useful markers but not ideal.
Mapped feature that are not genes are called DNA markers.
DNA markers must have at least two alleles to be useful.
DNA sequence features that satisfy this requirement are-
– Restriction Fragment Length Polymorphism (RFLP)
Southern hybridization
PCR
– Simple Sequence Length Polymorphism (SSLP)
– Single Nucleotide Polymorphism (SNP)
Mapping- determining the location of elements with in a genome, with respect to identifiable land marks.
Gene mapping describes the methods used to identify the locus of a gene and the distances between genes.
In simple mapping of genes to specific locations on chromosomes.
Two types
Genetic map
Physical Map
They are useful in predicting results of dihybrid and trihybrid crosses.
It allows geneticists to understand the overall complexity and genetic organization of a particular species.
Identify genes responsible for diseases.
Identify genes responsible for traits.
genetic maps are useful from an evolutionary point of view.
Genetic code is a dictionary that corresponds with sequence of nucleotides and sequence of amino acids.
Genetic code is a set of rules by which information encoded in genetic material(DNA or RNA sequences) is translated into proteins by living cells.
Term given By ″ Goerge Gamow ʺ
Dr. B. Victor is a retired biology professor with over 32 years of experience teaching and researching reproductive technology in fishes. His presentation outlines various forms of reproduction including asexual, sexual, and parthenogenesis. It also discusses cloning technology such as embryo splitting, nuclear transfer, and the three main types of cloning - recombinant DNA cloning, reproductive cloning, and therapeutic cloning. The benefits and applications of cloning as well as techniques for transgenic animal production are also summarized.
The document provides information and instructions for an upcoming exam. It advises students to arrive early to review and relax, as arriving even a minute late could result in a zero grade. All personal items must be placed at the front of the room, and only a pencil and eraser are allowed during the exam. Use of any electronic devices will result in a zero. Students must write their name on the exam paper and Scantron, and bring a photo ID and student number to turn in the materials. Answer keys will be posted after the exam without photos allowed. Grades will be posted as soon as possible. Cheating is strictly prohibited.
The document provides an overview of the reproductive systems of vertebrates. It describes the general structures and functions of the male and female reproductive systems. Key points include: 1) The female system produces eggs and houses the embryo, while the male system produces sperm. 2) Structures such as ovaries, oviducts, uterus, and vagina are present across vertebrate classes with some variations. 3) Testes, ducts and accessory glands are the main male structures. 4) Fertilization and copulation methods vary between external in frogs to internal in mammals. 5) The cloaca is modified in different groups, remaining primitive in some and separating functions in others like mammals.
Polytene chromosomes are large chromosomes formed through repeated DNA replication without cell division in specialized cells like the salivary glands of Drosophila melanogaster. This process produces many sister chromatids that remain attached, increasing cell volume. Polytene chromosomes were first observed in insect larvae and are characterized by distinctive light and dark banding patterns that can be used to identify genetic changes. They provide benefits like high gene expression levels and have been useful for studying chromatin structure and genomic equivalence in organisms.
DNA barcoding uses a short, standardized gene sequence from a uniform region of mitochondrial or nuclear DNA to identify species. It has potential to identify the estimated 10 million eukaryotic species on Earth. The cytochrome c oxidase I (COI) gene region is commonly used for animals. DNA barcoding can identify specimens at all life stages, resolve taxonomic ambiguities, and enable development of electronic field guides. It involves tissue sampling, DNA extraction and amplification, sequencing, and comparing sequences to reference databases. Costs and time for the process are decreasing with new technologies. Global efforts aim to compile barcodes for all known eukaryotes.
Gene mapping | Genetic map | Physical Map | DNA Data Analysis (upgraded)NARC, Islamabad
Genes are useful markers but not ideal.
Mapped feature that are not genes are called DNA markers.
DNA markers must have at least two alleles to be useful.
DNA sequence features that satisfy this requirement are-
– Restriction Fragment Length Polymorphism (RFLP)
Southern hybridization
PCR
– Simple Sequence Length Polymorphism (SSLP)
– Single Nucleotide Polymorphism (SNP)
Mapping- determining the location of elements with in a genome, with respect to identifiable land marks.
Gene mapping describes the methods used to identify the locus of a gene and the distances between genes.
In simple mapping of genes to specific locations on chromosomes.
Two types
Genetic map
Physical Map
They are useful in predicting results of dihybrid and trihybrid crosses.
It allows geneticists to understand the overall complexity and genetic organization of a particular species.
Identify genes responsible for diseases.
Identify genes responsible for traits.
genetic maps are useful from an evolutionary point of view.
Genetic code is a dictionary that corresponds with sequence of nucleotides and sequence of amino acids.
Genetic code is a set of rules by which information encoded in genetic material(DNA or RNA sequences) is translated into proteins by living cells.
Term given By ″ Goerge Gamow ʺ
Dr. B. Victor is a retired biology professor with over 32 years of experience teaching and researching reproductive technology in fishes. His presentation outlines various forms of reproduction including asexual, sexual, and parthenogenesis. It also discusses cloning technology such as embryo splitting, nuclear transfer, and the three main types of cloning - recombinant DNA cloning, reproductive cloning, and therapeutic cloning. The benefits and applications of cloning as well as techniques for transgenic animal production are also summarized.
DNA barcoding is a standardized approach to identifying plants and animals by minimal sequences of DNA, called DNA barcodes.
DNA barcode - short gene sequences taken from a standardized portion of the genome that is used to identify species
and this presentation gives much introducing about DNA barcodes developed for Prokaryotes and Eukaryotes.
Various barcoding genes which are evolutionary conserved.
techniques to develop a DNA bar-code and its future perspectives
Current technologies and future technologies of DNA barcoding. Applications regarding environment awareness. it also contains 2-3 case studies
This document discusses DNA barcoding, which is a technique for species identification using short DNA sequences. DNA barcoding uses a standard fragment of the mitochondrial cytochrome c oxidase subunit I (COI) gene to identify species. The technique was formally proposed in 2003 and has since been developed by organizations like the International Barcode of Life project to create a global reference library. DNA barcoding is now used for applications like conservation, pest identification, food safety, and forensics.
This document discusses the C-Value Paradox, which is the observation that there is no correlation between the complexity of an organism and the amount of DNA (C-value) in its genome. The document provides examples showing that C-values, or the amount of DNA per haploid cell, can vary widely both within and across species, from 105 base pairs in mycoplasma to over 109 base pairs in mammals. While complexity tends to increase with higher C-values, exceptions exist, demonstrating there is no direct linear relationship between genome size and organism complexity. The term "C-value" refers to the haploid DNA content of a species.
Changes In Number And Structure Of Chromosomes SMGsajigeorge64
A brief account of the changes in number and structure of chromosomes : Haploidy, Polyploidy, Aneuploidy, Deletion, Duplication, Inversion and Translocation
Basic concepts in developmental biologydrammarmehdi
Cell differentiation allows for the formation of distinct cell types through differential gene expression. A cell's fate and potency become progressively restricted through developmental commitments in response to cytoplasmic determinants or inductive signals from other cells. Pattern formation organizes cells in the embryo according to their position through mechanisms like morphogen gradients, which establish regional identities and compartments that segment the body plan.
A DNA library is a collection of cloned restriction fragments of the DNA of an organism.
Two kinds of libraries will be discussed: genomic libraries and complementary DNA (cDNA) libraries.
Genomic libraries ideally contain a copy of every DNA nucleotide sequence in the genome.
In contrast, cDNA libraries contain those DNA sequences that appear as mRNA molecules, and these differ from one cell type to another.
This document provides an overview of different DNA typing methods used in forensic analysis, including their history, techniques, uses, and key developments. It discusses early methods like Restriction Fragment Length Polymorphism (RFLP) analysis and how newer Short Tandem Repeat (STR) analysis allows analysis from smaller DNA samples. STR analysis examines repeat regions that are highly variable between individuals. Additional methods covered include mitochondrial DNA analysis, Y-chromosome STR analysis, low copy number DNA analysis, and the use of CODIS for DNA databases. Key applications of DNA typing include criminal investigations, immigration eligibility, paternity testing, and medical and population genetics research.
1. DNA polymorphisms, such as single nucleotide polymorphisms (SNPs) and variable number tandem repeats (VNTRs), are natural variations in DNA sequences among individuals.
2. These polymorphisms can be used for indirect DNA diagnosis of genetic diseases through detection of restriction fragment length polymorphisms (RFLPs). DNA from family members is digested with restriction enzymes and analyzed through gel electrophoresis and Southern blotting.
3. If a polymorphism is found near a disease-causing mutation and is linked to it, its inheritance pattern can help determine which family members have inherited the mutation and are at risk for the associated genetic disease.
1. Meroblastic cleavage is incomplete cell division that occurs in eggs with large amounts of yolk, like those of reptiles and birds. It results in two main types - discoidal cleavage, restricted to the cytoplasmic disc, and superficial cleavage, limited to the thin surface area.
2. During gastrulation, massive cell proliferation, movement and rearrangement occurs in the blastula, forming the three germ layers - ectoderm, endoderm and mesoderm. This involves morphogenetic cell movements that shape the embryo and form the archenteron cavity.
3. Types of morphogenetic movements include epiboly such as extension and intercalation that thin and spread
This document provides an overview of genome organization in viruses, prokaryotes, and eukaryotes. It discusses the differences between DNA and RNA, various structural forms of DNA, and levels of genome organization. In viruses, genomes can be single or double-stranded DNA or RNA, linear or circular, and range in size from 2,000 to 2,000,000 base pairs. Prokaryotic genomes are typically single, circular chromosomes that are organized via nucleoid formation, supercoiling, and DNA looping. Eukaryotic genomes are located in the nucleus and mitochondria, arranged in linear chromosomes via interactions with histone proteins to form nucleosomes, chromatin fibers, euchromatin, and heter
The horseshoe crab Limulus polyphemus is an ancient genus that has changed little in over 250 million years. It is more closely related to chelicerates than crustaceans. Its body consists of a prosoma with six pairs of legs and two types of eyes, and an opisthosoma with six pairs of appendages that aid in respiration, reproduction, and locomotion. The first pair forms a genital operculum and the remaining five pairs are modified into gills. Horseshoe crabs are long-lived for invertebrates, with males maturing between 9-11 years and females between 10-12 years.
PCR is a technique used to amplify specific DNA sequences. It involves using DNA polymerase to replicate target DNA sequences across multiple temperature cycles. Key points:
1. PCR amplifies specific DNA segments through repeated cycles of heating and cooling. This allows millions of copies of the target DNA to be generated.
2. It was invented by Kary Mullis in 1983 and revolutionized molecular biology. Mullis shared the 1993 Nobel Prize in Chemistry for his invention.
3. PCR has many applications including pathogen detection, genetic testing, forensics, and molecular cloning. It is a core technique in molecular biology and genetics research.
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.
The document summarizes tissue engineering of the skin. It describes the three layers of skin - epidermis, dermis and subcutaneous layer. It then discusses current methods for treating severe burns, including skin grafts. Skin engineering is presented as an alternative where skin cells are grown in vitro on scaffolds, with three categories - epidermal, dermal and dermo-epidermal substitutes. The process of skin engineering and some current products like Integra are outlined. Limitations and the future of more advanced skin substitutes that better mimic real skin are also mentioned.
cell lineage , cell fate - diverse class of cell fate, cell fate in plant meristem, mammalian development cell fate, nutritional effects on epigenetics, epigenetics of plants,
control of cell fate.
Mutations are changes or alterations in the DNA sequence that can disrupt genes and alter protein production. Mutations can occur during sexual or asexual reproduction and be inherited or non-inherited. Causes of mutation include heredity, carcinogens like chemicals and radiation, and chance mistakes during DNA replication. Major types of mutations include transposons that insert into chromosomes, crossover failures in meiosis, and single gene mutations like substitutions where nucleotides are replaced or deletions where nucleotides are removed. The results of mutations can include genetic variation and hereditary disorders or cancer depending on if they are inherited or non-inherited.
This document discusses various chromosome banding techniques used to identify chromosomes and detect abnormalities. It describes:
1) Karyotyping, which analyzes chromosome morphology, and how it is used to compare relatedness between species.
2) Banding techniques that selectively stain regions of chromosomes based on DNA composition, allowing identification. These include Q, G, R, C, and T bands.
3) The techniques involve staining with fluorescent dyes or Giemsa followed by heat/chemical treatments to differentially darken bands for analysis under microscopes. Banding patterns are consistent and chromosome-specific.
This document provides information about population genetics and the Hardy-Weinberg principle of genetic equilibrium. It defines key population genetics concepts such as gene pool, allele frequencies, and genotypes. It describes the five conditions required for Hardy-Weinberg equilibrium: large population size, random mating, no mutations, no migration, and no natural selection. Examples are provided to demonstrate how to calculate allele and genotype frequencies using the Hardy-Weinberg equation.
This document contains information about Hardy-Weinberg equilibrium and natural selection. It includes 10 multiple choice questions about Hardy-Weinberg equilibrium concepts like allele frequencies and genotype frequencies. It also includes 10 multiple choice questions about different types of natural selection like directional, disruptive, and stabilizing selection. Examples are provided for each type of natural selection.
DNA barcoding is a standardized approach to identifying plants and animals by minimal sequences of DNA, called DNA barcodes.
DNA barcode - short gene sequences taken from a standardized portion of the genome that is used to identify species
and this presentation gives much introducing about DNA barcodes developed for Prokaryotes and Eukaryotes.
Various barcoding genes which are evolutionary conserved.
techniques to develop a DNA bar-code and its future perspectives
Current technologies and future technologies of DNA barcoding. Applications regarding environment awareness. it also contains 2-3 case studies
This document discusses DNA barcoding, which is a technique for species identification using short DNA sequences. DNA barcoding uses a standard fragment of the mitochondrial cytochrome c oxidase subunit I (COI) gene to identify species. The technique was formally proposed in 2003 and has since been developed by organizations like the International Barcode of Life project to create a global reference library. DNA barcoding is now used for applications like conservation, pest identification, food safety, and forensics.
This document discusses the C-Value Paradox, which is the observation that there is no correlation between the complexity of an organism and the amount of DNA (C-value) in its genome. The document provides examples showing that C-values, or the amount of DNA per haploid cell, can vary widely both within and across species, from 105 base pairs in mycoplasma to over 109 base pairs in mammals. While complexity tends to increase with higher C-values, exceptions exist, demonstrating there is no direct linear relationship between genome size and organism complexity. The term "C-value" refers to the haploid DNA content of a species.
Changes In Number And Structure Of Chromosomes SMGsajigeorge64
A brief account of the changes in number and structure of chromosomes : Haploidy, Polyploidy, Aneuploidy, Deletion, Duplication, Inversion and Translocation
Basic concepts in developmental biologydrammarmehdi
Cell differentiation allows for the formation of distinct cell types through differential gene expression. A cell's fate and potency become progressively restricted through developmental commitments in response to cytoplasmic determinants or inductive signals from other cells. Pattern formation organizes cells in the embryo according to their position through mechanisms like morphogen gradients, which establish regional identities and compartments that segment the body plan.
A DNA library is a collection of cloned restriction fragments of the DNA of an organism.
Two kinds of libraries will be discussed: genomic libraries and complementary DNA (cDNA) libraries.
Genomic libraries ideally contain a copy of every DNA nucleotide sequence in the genome.
In contrast, cDNA libraries contain those DNA sequences that appear as mRNA molecules, and these differ from one cell type to another.
This document provides an overview of different DNA typing methods used in forensic analysis, including their history, techniques, uses, and key developments. It discusses early methods like Restriction Fragment Length Polymorphism (RFLP) analysis and how newer Short Tandem Repeat (STR) analysis allows analysis from smaller DNA samples. STR analysis examines repeat regions that are highly variable between individuals. Additional methods covered include mitochondrial DNA analysis, Y-chromosome STR analysis, low copy number DNA analysis, and the use of CODIS for DNA databases. Key applications of DNA typing include criminal investigations, immigration eligibility, paternity testing, and medical and population genetics research.
1. DNA polymorphisms, such as single nucleotide polymorphisms (SNPs) and variable number tandem repeats (VNTRs), are natural variations in DNA sequences among individuals.
2. These polymorphisms can be used for indirect DNA diagnosis of genetic diseases through detection of restriction fragment length polymorphisms (RFLPs). DNA from family members is digested with restriction enzymes and analyzed through gel electrophoresis and Southern blotting.
3. If a polymorphism is found near a disease-causing mutation and is linked to it, its inheritance pattern can help determine which family members have inherited the mutation and are at risk for the associated genetic disease.
1. Meroblastic cleavage is incomplete cell division that occurs in eggs with large amounts of yolk, like those of reptiles and birds. It results in two main types - discoidal cleavage, restricted to the cytoplasmic disc, and superficial cleavage, limited to the thin surface area.
2. During gastrulation, massive cell proliferation, movement and rearrangement occurs in the blastula, forming the three germ layers - ectoderm, endoderm and mesoderm. This involves morphogenetic cell movements that shape the embryo and form the archenteron cavity.
3. Types of morphogenetic movements include epiboly such as extension and intercalation that thin and spread
This document provides an overview of genome organization in viruses, prokaryotes, and eukaryotes. It discusses the differences between DNA and RNA, various structural forms of DNA, and levels of genome organization. In viruses, genomes can be single or double-stranded DNA or RNA, linear or circular, and range in size from 2,000 to 2,000,000 base pairs. Prokaryotic genomes are typically single, circular chromosomes that are organized via nucleoid formation, supercoiling, and DNA looping. Eukaryotic genomes are located in the nucleus and mitochondria, arranged in linear chromosomes via interactions with histone proteins to form nucleosomes, chromatin fibers, euchromatin, and heter
The horseshoe crab Limulus polyphemus is an ancient genus that has changed little in over 250 million years. It is more closely related to chelicerates than crustaceans. Its body consists of a prosoma with six pairs of legs and two types of eyes, and an opisthosoma with six pairs of appendages that aid in respiration, reproduction, and locomotion. The first pair forms a genital operculum and the remaining five pairs are modified into gills. Horseshoe crabs are long-lived for invertebrates, with males maturing between 9-11 years and females between 10-12 years.
PCR is a technique used to amplify specific DNA sequences. It involves using DNA polymerase to replicate target DNA sequences across multiple temperature cycles. Key points:
1. PCR amplifies specific DNA segments through repeated cycles of heating and cooling. This allows millions of copies of the target DNA to be generated.
2. It was invented by Kary Mullis in 1983 and revolutionized molecular biology. Mullis shared the 1993 Nobel Prize in Chemistry for his invention.
3. PCR has many applications including pathogen detection, genetic testing, forensics, and molecular cloning. It is a core technique in molecular biology and genetics research.
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.
The document summarizes tissue engineering of the skin. It describes the three layers of skin - epidermis, dermis and subcutaneous layer. It then discusses current methods for treating severe burns, including skin grafts. Skin engineering is presented as an alternative where skin cells are grown in vitro on scaffolds, with three categories - epidermal, dermal and dermo-epidermal substitutes. The process of skin engineering and some current products like Integra are outlined. Limitations and the future of more advanced skin substitutes that better mimic real skin are also mentioned.
cell lineage , cell fate - diverse class of cell fate, cell fate in plant meristem, mammalian development cell fate, nutritional effects on epigenetics, epigenetics of plants,
control of cell fate.
Mutations are changes or alterations in the DNA sequence that can disrupt genes and alter protein production. Mutations can occur during sexual or asexual reproduction and be inherited or non-inherited. Causes of mutation include heredity, carcinogens like chemicals and radiation, and chance mistakes during DNA replication. Major types of mutations include transposons that insert into chromosomes, crossover failures in meiosis, and single gene mutations like substitutions where nucleotides are replaced or deletions where nucleotides are removed. The results of mutations can include genetic variation and hereditary disorders or cancer depending on if they are inherited or non-inherited.
This document discusses various chromosome banding techniques used to identify chromosomes and detect abnormalities. It describes:
1) Karyotyping, which analyzes chromosome morphology, and how it is used to compare relatedness between species.
2) Banding techniques that selectively stain regions of chromosomes based on DNA composition, allowing identification. These include Q, G, R, C, and T bands.
3) The techniques involve staining with fluorescent dyes or Giemsa followed by heat/chemical treatments to differentially darken bands for analysis under microscopes. Banding patterns are consistent and chromosome-specific.
This document provides information about population genetics and the Hardy-Weinberg principle of genetic equilibrium. It defines key population genetics concepts such as gene pool, allele frequencies, and genotypes. It describes the five conditions required for Hardy-Weinberg equilibrium: large population size, random mating, no mutations, no migration, and no natural selection. Examples are provided to demonstrate how to calculate allele and genotype frequencies using the Hardy-Weinberg equation.
This document contains information about Hardy-Weinberg equilibrium and natural selection. It includes 10 multiple choice questions about Hardy-Weinberg equilibrium concepts like allele frequencies and genotype frequencies. It also includes 10 multiple choice questions about different types of natural selection like directional, disruptive, and stabilizing selection. Examples are provided for each type of natural selection.
Hardy-Weinberg-Castle Principle of EquilibriumHenry Sergio Jr
The Hardy-Weinberg-Castle Principle states that under conditions of large population size, no mutation, no immigration or emigration, random mating, and random reproductive success, allelic and phenotypic frequencies will remain constant across generations. Natural populations rarely meet all these conditions, experiencing factors like non-random mating and selective pressures that drive evolution by changing frequencies over time. Studying this principle proves that natural selection is necessary for evolution and allows measurement of selective effects by comparing actual and expected allelic or phenotypic frequencies.
The document discusses key concepts related to gene pools and Hardy-Weinberg equilibrium. It defines a gene pool as the total set of genes in a population and explains that gene and genotype frequencies can be used to describe the proportions of alleles and genotypes in a population. The Hardy-Weinberg law states that allele frequencies will remain constant across generations if a population is large, randomly mating and experiences no evolutionary influences. The document provides an example calculation of expected genotype frequencies based on known allele frequencies according to the Hardy-Weinberg model.
B.sc. agri i pog unit 4 population geneticsRai University
This document provides an overview of population genetics and principles of evolution. It discusses how genetic variation is maintained in populations through mechanisms such as sexual reproduction, genetic drift, mutation and natural selection. A key concept is that evolution occurs through changes in allele frequencies in populations over generations. The document also covers Mendelian inheritance, Darwinian evolution, the Hardy-Weinberg principle of genetic equilibrium, and factors that can lead to deviations from equilibrium, driving microevolutionary changes within populations.
The document discusses the Hardy-Weinberg law, which states that allele and genotype frequencies in a population remain constant from generation to generation if the population meets certain conditions. These conditions include large population size, random mating, no mutations, no migration, and no natural selection. The Hardy-Weinberg equations can be used to calculate expected genotype frequencies based on allele frequencies in populations that are in Hardy-Weinberg equilibrium. Two examples are provided to demonstrate calculating allele and genotype frequencies.
The document discusses the Hardy-Weinberg law of genetic equilibrium. It states that the law describes how allele and genotype frequencies in a population remain constant from generation to generation if the population meets five assumptions: large population size, random mating, no mutations, no migration, and no natural selection. It provides examples of using the Hardy-Weinberg equations to calculate allele and genotype frequencies for populations of rats and cattle.
The evolution of populations population geneticsStephanie Beck
This document discusses population genetics and the Hardy-Weinberg theorem. It defines key terms like population, gene pool, allele frequency, and microevolution. The Hardy-Weinberg theorem states that allele frequencies will remain constant between generations if a population is large, random mating occurs, there is no mutation, migration or natural selection. The document provides examples of how to use the Hardy-Weinberg equation to calculate allele frequencies and genotype proportions in populations.
1) The document discusses Hardy-Weinberg equilibrium, which states that allele and genotype frequencies in a population remain constant from generation to generation if the population is large, randomly mating, and not experiencing selection, migration, mutation or genetic drift.
2) It provides an example showing how the frequencies of genotypes AA, Aa and aa are calculated based on the allele frequencies p and q in the parental generation.
3) The document explains that under Hardy-Weinberg equilibrium, the allele frequencies p and q will remain the same in subsequent generations, even as the specific genotype frequencies may change during mating.
The Hardy-Weinberg law states that gene frequencies in a population will remain constant from generation to generation if the population is large, randomly mating, and experiences no evolutionary influences like mutation, migration, or natural selection. The law can be represented through a simple formula and is used to calculate the expected frequencies of genotypes in a population based on the gene frequencies. It provides a foundation for studying population genetics and evolution through a mathematical approach.
This document discusses measuring evolution in populations through changes in allele frequencies over time. It introduces the five main agents that can cause such changes: mutation, gene flow, genetic drift, selection, and non-random mating. It then explains key concepts like populations, gene pools, and allele frequencies. Finally, it outlines Hardy-Weinberg equilibrium, which models a hypothetical non-evolving population, and the Hardy-Weinberg theorem which provides a way to calculate genotype frequencies based on allele frequencies.
The document discusses the Hardy-Weinberg principle of population genetics. It states that the frequency of alleles in a population will remain constant over generations if the population is large, randomly mating, and not subject to mutations, gene flow, or selection pressures. It provides an example using cat coat color alleles to demonstrate calculating genotype frequencies based on observed phenotypes and applying the Hardy-Weinberg equations. Factors that can disrupt Hardy-Weinberg equilibrium and cause allele frequencies to change are also noted, including mutation, migration, natural selection, and genetic drift.
The document discusses the Hardy-Weinberg equation, which relates allele and genotype frequencies in a population at genetic equilibrium. It describes how the equation predicts that allele and genotype frequencies will remain constant from generation to generation if certain conditions are met, including no mutations, natural selection, migration, genetic drift or non-random mating. It provides examples of using the Hardy-Weinberg equation to calculate expected genotype and allele frequencies based on observed data from populations of horses and butterflies.
Population genetics reconciled Darwin and Mendel's ideas by showing how natural selection could act on variation present in populations. The Hardy-Weinberg theorem describes genetic equilibrium in a population where allele frequencies remain constant between generations unless disrupted by factors like genetic drift, migration, non-random mating, mutation, or natural selection. These disruptions to equilibrium allow for microevolution and populations to change over time through natural selection acting on genetic variation.
Foundations of Biological Sciences I Evolutionary Agents - 1 .docxbudbarber38650
Foundations of Biological Sciences I Evolutionary Agents - 1
A quick recap….
There are several terms that need to be clarified so that you can more easily follow the exercise. A gene is a
piece of DNA that directs the expression of a particular characteristic (trait). Genes are located on
chromosomes, and the location where a particular gene is found is referred to as the locus (plural: loci) of that
gene. An allele is a gene for which there is an alternative expression, which can lead to the alterative form of a
trait. For example, a diploid organism carries the allele “A” on one homologous chromosome, and the allele “A”
on the other. The genotype of this organism is then AA and it is said to be homozygous. An organism may also
carry two different alleles. For example on one chromosome it could carry the allele “A” and on the other it
could carry the allele “a”. The genotype of such an organisms is then Aa, and it is described as heterozygous for
this chromosomal locus.
The genotype of an organism is the listing of the two alleles for each trait that it possesses. The phenotype of an
organism is a description of the way a trait is displayed in the structure, behavior, or physiology of the organism.
Some alleles are dominant to others and mask the presence of other alleles. The dominant condition is indicated
by uppercase letters (e.g., “A”). The alleles that are masked are called recessive alleles. The recessive condition
is indicated by lowercase letters (e.g., “a”). When both dominants are present in the genotype (AA), the organism
is said to be homozygous dominant for the trait, and the organisms will show the dominant phenotype (trait
expression A). When both recessives are present in the genotype (aa), the organism is said to be homozygous
recessive for the trait, and the organisms will show the recessive phenotype (trait expression a). In the case of
complete dominance, the dominant allele completely masks the recessive allele, and an organism with a
heterozygous genotype (Aa) will show the dominant phenotype (trait expression A).
Evolutionary Agents
Evolution is a process resulting in changes in gene frequencies (= the genetic make-up) of a population over
time. The mechanisms of evolution include selection (which can cause change over time & adaptation), and
forces that provide variation and cause change over time (but not adaptation). Factors that change gene
frequencies over time are referred to as evolutionary agents.
A powerful way to detect the presence of evolutionary agents is the use of the Hardy–Weinberg model. This
model can be applied to traits that are influenced by several loci; the simplest case is for a trait that is regulated
by one locus with two alleles.
With the Hardy–Weinberg model, the frequency of genotypes in the population can be predicted from the
probability of encounters between gametes bearing the different alleles. With alleles R .
This document discusses population genetics and key concepts in evolutionary biology. It covers Mendelian genetics, the Hardy-Weinberg principle of equilibrium, mechanisms of evolution like genetic variation, natural selection and genetic drift. It also discusses applications of population genetics like estimating allele frequencies, measuring genetic variation, and using DNA polymorphisms in forensics.
The document discusses several key concepts related to microevolution and population genetics, including:
- Gene pools and allelic frequencies changing over time through mutations, gene flow, genetic drift, and non-random mating can cause microevolution.
- Hardy-Weinberg principle states that allele frequencies remain stable in a population not experiencing these evolutionary forces.
- Types of natural selection include directional, stabilizing, and disruptive selection.
- Speciation occurs when reproductive isolation leads to the splitting of one species into two or more distinct species over time. Mechanisms of isolation can be prezygotic or postzygotic.
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HARDY –WEINBERG’S GROP SIX-1-1_113253.pptx
1. HARDY –WEINBERG’S
PRINCIPLE
GROUP SIX
ORYEM DIANA DIDI 22/U/6829
MUSENE REAGAN 22/U/3448/PS
KALYANGO BRIAN 21/U/0764
WAISWA DERRICK 22/U/7040
YOKWE LORDIN 22/U/3967/PS
KASIRYE ABDALAH SOWEDI
22/U/6076
2. Hardy- Weinberg equilibrium
Dr. Wilhelm Weinberg
(German Physician)
G.H Hardy ( British
mathematician)
This equilibrium was put forward by G.H. Hardy
and Dr. Weinberg in 1908 but independently
3. Hardy- Weinberg equilibrium states
that the gene and genotype
frequencies in a population will
remain constant from generation to
generation provided that the
population is large and interbreeding
occurs, mating is random, no
selection occurs, no emigration or
immigration occurs, and no
mutations occur
4. Conditions for Hardy Weinberg’s
principle
A large population size (small populations are more
susceptible to genetic drift)
No gene mutations may occur and therefore allele changes
do not occur.
There must be no migration of individuals either into or out
of the population.
Random mating must occur, meaning individuals mate by
chance.
No genetic drift, a chance change in allele frequency, may
occur.
No natural selection, a change in allele frequency due to
environment, may occur.
5. Limitations of the principle
Hardy-Weinberg Equilibrium never occurs in nature because there is always at
least one rule being violated. Hardy-Weinberg Equilibrium is an ideal state
that provides a baseline against which scientists measure gene evolution in a
given population.
6. Application of Hardy-Weinberg
1st – Determine the allele and genotypic frequencies of a population
2nd – Compare with the data that we actually observe for the population in
subsequent generations
Changes in allele frequencies provide evidence for the occurrence of
evolution in a population
Helps us to understand how and why human populations evolve over time
Used in medicine to determine the the probability of human matings that may
result in defective offsprings
7. Hardy-Weinberg Equations
The Hardy-Weinberg equations can be used for any population; the population
does not need to be in equilibrium.
There are two equations necessary to solve a Hardy-Weinberg Equilibrium
question:
𝑝 + 𝑞 = 1
𝑝² + 2𝑝𝑞 + 𝑞²
= 1
8. What do all those p’s and q’s mean???
p.= frequency of the dominant allele for a particular gene in a population
q.= frequency of the recessive allele for a particular gene in a population
p2 = frequency of homozygous dominant individuals within a population
2pq = frequency of heterozygous individuals within a population
q2 = frequency of homozygous recessive individuals within a population
9. Examples
Example 1a:
A population of cats can be either black or white; the black allele (B) has
complete dominance over the white allele (b). Given a population of 1,000 cats,
840 black and 160 white, determine the allele frequency, the frequency of
individuals per genotype, and number of individuals per genotype. solution
To solve this problem, solve for all the preceding variables (𝑝, 𝑞, 𝑝², 2𝑝𝑞, 𝑞²
Step 1: Find the frequency of white cats, the homozygous recessive genotype, as they have
only one genotype, bb. Black cats can have either the genotype Bb or the genotype BB, and
therefore, the frequency cannot be directly determined.
10. calculations
Frequency of white cats = 0.16; therefore, 𝑞² = 0.16
Step 2: Find 𝑞𝑞 by taking the square root of 𝑞².
√(𝑞²) = √(0.16)
𝑞 = 0.4
Step 3: Use the first Hardy-Weinberg equation (𝑝 + 𝑞 = 1) to solve for 𝑝.
𝑝 + 𝑞 = 1
𝑝 = 1 −𝑞
𝑝 = 1 − (0.4)
𝑝 = 0.6
Now that the allele frequencies in the population are known, solve for the remaining
frequency of individuals by using 𝑝² + 2𝑝𝑞 + 𝑞² = 1.
Step 4: Square 𝑝 to find 𝑝².
11. 𝑝 = 0.6
𝑝² = (0.6)²
𝑝² = 0.36
Step 5: Multiply 2 × 𝑝 × 𝑞 to get 2𝑝𝑞.
2𝑝𝑞 = 2(0.6)(0.4)
2𝑝𝑞 = 0.48 Therefore:
The frequency of the dominant alleles: 𝑝 = 0.6
The frequency of the recessive alleles: 𝑞 = 0.4
The frequency of individuals with the dominant genotype: 𝑝² = 0.36
The frequency of individuals with the heterozygous genotype: 2𝑝𝑞 = 0.48
The frequency of individuals with the recessive genotype: 𝑞² = 0.16
Remember: Frequencies can be checked by substituting the values above back into the
Hardy-Weinberg equations.
0.6 + 0.4 = 1
0.36 + 0.48 + 0.16 = 1
Step 6: Multiply the frequency of individuals (𝑝², 2𝑝𝑞, 𝑞²) by the total population to get the
number of individuals with that given genotype.
𝑝² × total population = 0.36 × 1,000 = 360 black cats, BB genotype
12. 2𝑝𝑞 × total population = 0.48 × 1,000 = 480 black cats, Bb genotype.
𝑞² × total population = 0.16 × 1,000 = 160 white cats, bb
genotype.
Comparing Generations
To know if a population is in Hardy-Weinberg Equilibrium scientists have
to observe at least two generations. If the allele frequencies are the same for
both generations then the population is in Hardy-Weinberg Equilibrium.
13. .
Example 1b:
Recall: the previous generation had allele frequencies of 𝑝 = 0.6 and 𝑞 = 0.4.
The next generation of cats has a total population of 800 cats, 672 black and 128 white. Is
the population in Hardy-Weinberg Equilibrium?
Step 1: Solve for 𝑞².
= 0.16
Step 2: Use 𝑞² to solve for 𝑞. There is no need to solve the entire equation, because if 𝑞 has
changed, then 𝑝 has also changed. If 𝑞 remains the same, then 𝑝 will remain the same.
𝑞² = 0.16
√(𝑞²) = √(0.16)
𝑞 = 0.4
Because the recessive allele frequency (𝑞) has remained the same, the population is in a state
of Hardy-Weinberg Equilibrium.
14. Example 2a:
The beak color of finches has a complete dominance relationship where black beaks are dominant
over yellow beaks. There are 210 individuals with the genotype DD, 245 individuals with the
genotype Dd and 45 individuals with the genotype dd.
Find: the frequency of the dominant and recessive alleles and the frequency of individuals with
dominant, heterozygous, and recessive traits.
Step 1: Add up all the individuals to calculate the total population.
210 + 245 + 45 = 500
Step 2: Find 𝑞².
= 0.09
15. Step 3: Take the square root of 𝑞² to find 𝑞.
𝑞² = 0.09
√(𝑞²) = √(0.09)
𝑞 = 0.3
Step 4: Use the first Hardy-Weinberg equation (𝑝 + 𝑞 = 1) to solve for 𝑝.
𝑝 + 𝑞 = 1
𝑝 = 1 − 𝑞
𝑝 = 1 − (0.3)
𝑝 = 0.7
Now that the allele frequencies in the population are known, solve for the frequency
of all individuals by using 𝑝² + 2𝑝𝑞 + 𝑞² = 1.
Step 5: Square 𝑝𝑝 to find 𝑝𝑝².
𝑝 = 0.7
𝑝² = (0.7)²
𝑝² = 0.49
Step 6: Multiply 2 × 𝑝 × 𝑞 to get 2𝑝𝑞.
2𝑝𝑞 = 2 × 0.7 × 0.3
16. 2𝑝𝑞 = 0.42
Therefore:
The frequency of the dominant alleles: 𝑝 = 0.7
The frequency of the recessive alleles: 𝑞 = 0.3
The frequency of individuals with the dominant genotype: 𝑝² = 0.49
The frequency of individuals with the heterozygous genotype: 2𝑝𝑞 = 0.42
The frequency of individuals with the recessive genotype: 𝑞² = 0.09
17. Example 2b:
The next generation of finches has a population of 400. There are 336 with black beaks and
64 with yellow beaks. Is this population in Hardy-Weinberg Equilibrium?
Step 1: Solve for 𝑞².
= 0.16
Step 2: Take the square root of 𝑞² to find 𝑞.
𝑞² = 0.16
√(𝑞²) = √(0.16)
𝑞 = 0.4
Because the recessive allele frequency (𝑞) has changed, the population is NOT in a state of
Hardy-Weinberg Equilibrium.
18. Practice questions
1. Scale coloration of lizards has a complete dominance relationship where green scales are
dominant over blue scales. There are 1,024 individuals with the genotype GG, 512
individuals with the genotype Gg, and 64 individuals with the genotype gg.
Find: the frequency of the dominant and recessive alleles and the frequency of individuals
with dominant, heterozygous, and recessive genotype.
2. The next generation of lizards has 1092 individuals with green scales and 108 individuals
with blue scales. Is the population in Hardy-Weinberg Equilibrium? Solve for p and q.
3. Rabbit’s ears can be either short or floppy, where short ears are dominant over floppy ears.
There are 653 individuals in a population. 104 rabbits have floppy ears and 549 have short
ears.
19. questions
Find: the frequency of the dominant and recessive alleles and the frequency of individuals
with dominant, heterozygous, and recessive genotypes.
1. The next generation of rabbits has 560 individuals with short ears and 840 individuals with
floppy ears. Is the population in Hardy-Weinberg Equilibrium? Solve for p and q.
2. Petal coloration of pea plants has a complete dominance relationship where purple petals are
dominant over white petals. There are 276 plants, 273 have purple petals.
Find: the frequency of the dominant and recessive alleles and the frequency of individuals
with the dominant, heterozygous, and recessive genotype.
3. The next generation of pea plants has 552 plants, 546 have purple petals. Is the population in
Hardy-Weinberg Equilibrium? Solve for p and q.