DNA (Deoxyribo nucleic acid) is the principal genetic material of all organisms, except some viruses.
In 1953, James Watson and Francis Crick proposed the structural model of DNA for which they received the Nobel Prize in 1962.
DNA Replication In Eukaryotes (Bsc.Zoology)DebaPrakash2
This Slide Is explanation of Mechanism of DNA Replication In Eukaryotes.
As we know we all have DNA as the genetic material and So we should know how this DNA getting Duplicated so that it'll pass to daughter cells.
DNA Replication In Eukaryotes (Bsc.Zoology)DebaPrakash2
This Slide Is explanation of Mechanism of DNA Replication In Eukaryotes.
As we know we all have DNA as the genetic material and So we should know how this DNA getting Duplicated so that it'll pass to daughter cells.
Molecular biology is the study of biology at a molecular level.
In broad sense, the study of gene structure and functions at the molecular level to understand the molecular basis of hereditary, genetic variation, and the expression patterns of genes.The field overlaps with other areas of biology and chemistry, particularly genetics and biochemistry.
DNA as a Genetic Material - Dr. P. Saranraj, Assistant Professor, Department of Microbiology, Sacred Heart College (Autonomous), Tirupattur, Vellore District, Tamil Nadu, India.
Hello There,
DNA Footprinting Is A Molecular Biology Technique With Wide Applications In Many Areas Of Biological Sciences And Importantly It Is Used For Crime Detection In Forensic Sciences. In This Presentation, You Will Learn What It Is, The Technology, Protocol, Pictorial Representation, Applications And References For Further Study.
This power point presentation explains double helical structure of DNA as proposed by Watson and Crick (1953).Attempts have also been made to high light the valuable contributions made by Rosalind Franklin and Wilkins. Brief details of different types of DNA have also been included.
Molecular biology is the study of biology at a molecular level.
In broad sense, the study of gene structure and functions at the molecular level to understand the molecular basis of hereditary, genetic variation, and the expression patterns of genes.The field overlaps with other areas of biology and chemistry, particularly genetics and biochemistry.
DNA as a Genetic Material - Dr. P. Saranraj, Assistant Professor, Department of Microbiology, Sacred Heart College (Autonomous), Tirupattur, Vellore District, Tamil Nadu, India.
Hello There,
DNA Footprinting Is A Molecular Biology Technique With Wide Applications In Many Areas Of Biological Sciences And Importantly It Is Used For Crime Detection In Forensic Sciences. In This Presentation, You Will Learn What It Is, The Technology, Protocol, Pictorial Representation, Applications And References For Further Study.
This power point presentation explains double helical structure of DNA as proposed by Watson and Crick (1953).Attempts have also been made to high light the valuable contributions made by Rosalind Franklin and Wilkins. Brief details of different types of DNA have also been included.
Deoxyribonucleic acid is a polymer composed of two polynucleotide chains that coil around each other to form a double helix. The polymer carries genetic instructions for the development, functioning, growth and reproduction of all known organisms and many viruses. DNA and ribonucleic acid are nucleic acids.
Nucleic acid-DNA and RNA
Gene-part of DNA
Functions of DNA
RNA-Functions, different types of RNA-Ribosomal RNAs (rRNAs), Messenger RNAs (mRNAs), Transfer RNAs (tRNAs)-Other RNA-Small nuclear RNA (snRNA), Micro RNA (miRNA), Small interfering RNA (siRNA), Heterogenous RNA (hnRNA).
Nucleic acid-nucleotides-nucleoside
Components of nucleotide-a nitrogenous (nitrogen-containing) base (pyrimidine and purine), (2) a pentose, and (3) a phosphate
Structure of pentose sugar, and 5 major bases (cytosine, thymine, uracil-pyrimidine bases and adenine, guanine-purine bases).
Deoxyribonucleotides and Ribo nucleotides-Molecular structure of deoxyadenosine monophosphate (dAMP), deoxyguanosine monophosphate (dGMP), deoxythymidine monophosphate (dTMP), deoxycytidine monophosphate (dCMP) and Adenosine monophosphate (AMP), Guanosine monophosphate (GMP), Cytosine monophosphate (CMP) and Uridine monophosphate (UMP), Watson crick base pairing, Hoogsteen base pairing,
Helical structure-Heterocylic N -Glycosides, Syn and Anti Conformers, detailed structure of single strand and double stranded DNA.
DNA Nucleotides and Tautomeric Form-Tautomers of Adenine, Cytosine, Guanine, and Thymine
Template strand, non coding strand and coding strand
Hydrogen bonds, phosphodiester linkage, hydrolysis of DNA and RNA.
Different forms of DNA-A, B, and Z forms.
Palindrome sequence, Linear DNA, Cruciform DNA, H DNA (Triplex DNA), Denaturation of DNA, Hyperchromicity, Tm, Renaturation of DNA, Tertiary structure of DNA, Difference of DNA and RNA, RNA structural elements, primary. secondary and tertiary structure of RNA. Detailed structure and functions of tRNA, mRNA, rRNA, miRNA, siRNA, hn RNA, snRNA.
Nucleic acid hybridization, C0t analysis, Buoyant density of DNA, Isopycnic centrifugation.
Double fertilization is the process found in angiosperms in which out of the two male gametes released inside the embryo sac, one fuses with the egg cell (syngamy) and another fuse with secondary nucleus (triple fusion).
Photosynthesis is an anabolic process by which simple inorganic substances like CO2 and H2O are converted into a complex substance like a carbohydrate in the presence of light and chlorophyll.
Genetics (Greek word ‘genesis’ = to grow into)
i. The branch of biology which deals with the study of heredity and variation is known as genetics.
ii. The term genetics were coined by Bateson (1906).
2. Heredity :
The transmission of character from one generation to the others is called as heredity.
Gregor Johann Mendel (July 20, 1822 – January 6, 1884) was a Czech-German Augustinian friar and scientist, who gained posthumous fame as the founder of the new science of genetics for his study of the inheritance of certain traits in pea plants. Mendel showed that the inheritance of these traits follows particular laws, which were later named after him. The significance of Mendel’s work was not recognized until the turn of the 20th century. The independent rediscovery of these laws formed the foundation of the modern science of genetics.
In incomplete dominance the genes of an allelomorphic pair are not expressed as dominant or recessive.
ii. They express them self partially when present together in hybrid.
iii. One gene cannot suppress the expression of the other completely.
iv. As a result F1, hybrid shows characters intermediate to the effect of two genes of the parent.
v. In such cases both the alleles of contrasting characters express as blend or mixing.
Mitosis is an equational division, dividing the mother cell into two daughter cells which are identical to one another and also to the mother cell in having the same number and kind of chromosome.
Meiosis is reductional division in which the chromosome number is reduced to half. During meiosis, four haploid daughter cells are formed from one parental cell.
It is a process in which the chromosomes duplicate only once but the cell divides twice.
It results in formation of four haploid cells. Hence, it is also called reduction division.
The lichens are slow growing, long living organisms.
Theophrastus was first to use the word lichen.
Lichens are formed by close association of two different partners,
A) Phycobiont or photobiont: The algal component of lichens is called phycobiont.
It mostly belong to Chlorophyceae(green algae)
Or cyanobacteria ( blue green algae)
B) Mycobiont: The fungal component of the lichens is called mycobiont. It belongs to ascomycetes and rearly Basidomycetes or Deuteromycetes.
Kingdom Fungi includes Unicellular ( Yeast) or multicellular and filamentous (Penicillium) organisms.
Unicellular organisms have a protoplast with many nuclei e.g. Rhizopus or with a single nucleus e.g. Yeast.
Filamentous organisms consist of a body called Mycelium in which a number of thread like structures called Hypae are present.
What is cell division?
Ans: Cell division is a process by which a cell divides into two or more daughter cells.
Every cell arises from the pre-existing cell by the process of cell division.
Q. What is generation time?
Ans: The period between two successive divisions is called generation time.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...
Dna as genetic material ppt
1. DNA as genetic material
Deparment Of Botany
Preapared by
Dr. P. B.Cholke
(Assistant Professor in Botany)
Pune District Education Association’s
Anantrao Pawar College ,Pirangut,
Tal-Mulshi, Dist-Pune- 412115
8. • DNA (Deoxyribo nucleic acid) is the principal
genetic material of all organisms, except some
viruses.
• In 1953, James Watson and Francis Crick
proposed the structural model of DNA for
which they received the Nobel Prize in 1962.
9.
10. Structure of DNA
• A) Double Helix :
a. The DNA molecule
consists of two strands
(chains).
• b. The two strands
are spirally coiled
around each other and
around a central
imaginary axis in a
regular manner to
form a double helix.
and shows alternating
major and minor
grooves.
11. B)Structure of each strand :
a. Each strand of DNA is a
polynucleotide chain, i.e. formed -of
many nucleotides.
b. The backbone of each strand
consists of alternating deoxyribose
sugar and phosphate groups.
c. Each phosphate group is
joined to 3rd carbon atom of one
deoxyribose sugar molecule and
5th carbon atom of successive
deoxyribose molecule of the same
strand by phospho-diester bond.
d. Each sugar in the strand has
one nitrogen base attached to it at 1st
carbon by glycosidic bond
12. C)Base Pairing :
a. The two strands are joined together by pairs of nitrogen bases.
b. In each pair, one base is always purine and the other base is
pyrimidine.
c. The base pairing is very specific. The purine base Adenine (A) of
one strand will always pair
with the pyrimidine base Thymine (T) of another strand. .
d. The purine base Guanine (G) of one strand always pairs with the
pyrimidine base Cytosine (C)
of another strand.
13. • The nitrogen containing
bases along with
hydrogen bonds make
up the rungs of the
ladder.
• These are also referred
to as transverse bars.
14. Chargaff’s rule
• Purine - Pyrimidine ratio :
a. In a DNA molecule, total number of A = total
number of T and total number of G = total
number of C. In other words, A + G = T + C. This is
called Chargaff's rule.
b.Thus, purine: pyrimidine ratio is 1 : 1.
c. It may be represented as follows :
or A + G =T + C.
A G
T C
1
15. Polarity
• F) Polarity of strands :
• Both the polynucleotide strands of
DNA show polarity, i.e. direction.
• One end of each strand has a free' –
OH' group at 3rd carbon of
deoxyribose sugar.
• This end of the strand is called 3' end
or C–3. It is not linked to any
nucleotide.
• Other end of the strand has a free
phosphate group at 5th carbon atom
of the deoxyribose sugar.
• This end of the strand is called 5' end
or C– 5. It is also not linked to any
nucleotide.
• One strand of DNA is oriented in 3'–5'
and complementary strand is
oriented in 5'–3' manner
Fig. Structure of DNA (Watson and Crick model)
16. Antiparallel strand
• G) Antiparallel strands :
• The two strands of DNA
are parallel to each other,
but are placed in opposite
direction.
• One strand runs in (5' to 3')
direction, while the other
in (3' to 5') direction.
• Such strands are called
antiparallel strands.
17. Dimentions
• Dimensions :
a. The diameter of a DNA molecule is
20 nm (20 A)o . It remains constant
throughout the length of DNA.
b. The length of one complete turn
(spiral or gyre or pitch) is 3.4nm
(34 Ao). One turn is the distance
between two successive major
grooves or minor grooves.
c. In one complete turn of DNA, 10
base pairs are present.
d. Therefore, the distance between
the successive base pairs is 0.34
nm (3.4 Ao).
Fig. Structure of DNA (Watson and Crick model)