GENETIC MATERIAL refers to the material of which genes are made up of. It includes both DNA and RNA. Though in most of the organism DNA is playing this role, but in certain viruses RNA is storing all the genetic information of the individual. Here we are discussing about the discovery and property of these genetic material.
DNA is tightly packed in the nucleus of every cell. DNA wraps around special proteins called histones, which form loops of DNA called nucleosomes. These nucleosomes coil and stack together to form fibers called chromatin. Chromatin in turn forms larger loops and coils to form chromosomes.
DNA packaging is crucial because it makes sure that those excessive DNA are able to fit nicely in a cell that is many times smaller.
The DNA in bacterial cells are either circular or linear. To accommodate the size of bacterial cell, supercoiled DNA are folded into loops with each loop resembles shape of bead-like packets containing small basic proteins that is analogous to histone found in Eukaryotes.
This power point presentation is an attempt to present some direct and some indirect evidences in favour of DNA as genetic material. Very few organisms have RNA as genetic material for example plant virus and some bacteriophages
DNA as a Genetic Material - Dr. P. Saranraj, Assistant Professor, Department of Microbiology, Sacred Heart College (Autonomous), Tirupattur, Vellore District, Tamil Nadu, India.
DNA is tightly packed in the nucleus of every cell. DNA wraps around special proteins called histones, which form loops of DNA called nucleosomes. These nucleosomes coil and stack together to form fibers called chromatin. Chromatin in turn forms larger loops and coils to form chromosomes.
DNA packaging is crucial because it makes sure that those excessive DNA are able to fit nicely in a cell that is many times smaller.
The DNA in bacterial cells are either circular or linear. To accommodate the size of bacterial cell, supercoiled DNA are folded into loops with each loop resembles shape of bead-like packets containing small basic proteins that is analogous to histone found in Eukaryotes.
This power point presentation is an attempt to present some direct and some indirect evidences in favour of DNA as genetic material. Very few organisms have RNA as genetic material for example plant virus and some bacteriophages
DNA as a Genetic Material - Dr. P. Saranraj, Assistant Professor, Department of Microbiology, Sacred Heart College (Autonomous), Tirupattur, Vellore District, Tamil Nadu, India.
A complementation test (sometimes called a "cis-trans" test) can be used to test whether the mutations in two strains are in different genes. By taking an example of Benzer's work, complementation has been explained.
The genetic material of a cell or an organism refers to those materials found in the nucleus, mitochondria and cytoplasm, which play a fundamental role in determining the structure and nature of cell substances, and capable of self-propagating and variation.
Chromatin is the complex combination of DNA and proteins that makes up chromosomes. It can be made visible by staining with specific techniques and stain (thus the name chromatin which literally means colored material). The major proteins involved in chromatin are histone proteins; although many other chromosomal proteins have prominent roles too. The functions of chromatin is to package DNA into smaller volume to fit in the cell, to strengthen the DNA to allow mitosis and meiosis and to serve as a mechanism to control gene expression and DNA replication.
A complementation test (sometimes called a "cis-trans" test) can be used to test whether the mutations in two strains are in different genes. By taking an example of Benzer's work, complementation has been explained.
The genetic material of a cell or an organism refers to those materials found in the nucleus, mitochondria and cytoplasm, which play a fundamental role in determining the structure and nature of cell substances, and capable of self-propagating and variation.
Chromatin is the complex combination of DNA and proteins that makes up chromosomes. It can be made visible by staining with specific techniques and stain (thus the name chromatin which literally means colored material). The major proteins involved in chromatin are histone proteins; although many other chromosomal proteins have prominent roles too. The functions of chromatin is to package DNA into smaller volume to fit in the cell, to strengthen the DNA to allow mitosis and meiosis and to serve as a mechanism to control gene expression and DNA replication.
Genetic material
Anant Mohan Sharma
All cell have the capability to give rise to the cell and
the encoded information in living cell is passed from
one generation to another. The information encoded
material is the genetic material or hereditary material
of the cell.
The genetic material is long sequence of nucleic
acids that contain the genetic instruction. Nucleic
acid are macromolecules in the form of DNA or
RNA.
Experimental evidences
Griffith’s experiment
Avery, MacLeod &McCarty experiment
Hershey & Chase experiment
RNA as genetic material
DNA structure
Z- DNA
V. Sasisekharan RL model
Types of RNA
DNA is a double helical structure that transfers the genetic information from one generation to another. it consists of two strands with the four nucleotide basis .The four nucleotides contains adenine, cytosine, guanine, thymine .These four nuclic basis are such arranged and coiled with the help of hydrogen bonds and forms the helical structure of DNA. In RNA the thymine is replaced with uracil. Here you will learn the replication ,transcription and translation process in DNA.
DNA- deoxyribonucleic acid
A long molecule that looks like a twisted ladder made up of four types of simple units and the sequence of these units carries genetic information.
Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA).
genetic material in organization, Central dogma,transcription in prokaryotes ...Patelrushi11
Historical background of molecular genetics, genetics material in organisams- Experiments, Nucleic acid as genetic material, central dogma, transcription in prokaryotes eukaryotes, genetic codegenetic code and its characteristics, silent feature of genetic codon,wobbal hypothesis
Cross- pollinated crops are highly heterozygous due to the free intermating among their plants. They are often referred to as random mating populations because each individual of the population has equal opportunity of mating with any other individual of that population. Such a population is also known as Mendelian population or panmictic population. A population, in this case, consists of all such individuals that share the same gene pool, i.e., have an opportunity to intermate with each other and contribute to the next generation of the population. To understand the genetic make - up of such populations a sophisticated field of study, population genetics, has been developed. The Hardy Weinberg law states that in a large random mating population gene and genotype frequency remain constant generation after generation unless there is selection, mutation, migration or random drift. This is the fundamental law of population genetics and provides the basis for studying Mendelian populations. The law is proposed independently by G. H. Hardy (a mathematician) and W. Weinberg (a physician).
The genetic material must produce a large number of copies of itself during the life cycle of an organism. The process by which a DNA molecule makes its identical copies is called DNA replication. The DNA molecule that undergoes replication may be termed as ‘parent molecule or template molecule, while the two molecules produced by replication may be called progeny molecules or daughter molecules.
The base sequence information present in the gene (DNA) is copied into an RNA molecule, which directly participates in protein synthesis and provides information for amino acid sequence of the protein. This RNA molecule is called messenger RNA or mRNA. The process of production of RNA copy of a DNA sequence is called transcription; this reaction is catalyzed by DNA-directed RNA polymerase, or simply RNA polymerase.
The information for the proteins found in a cell is encoded in genes of the genome of the cell. A protein- coding gene is expressed by the process of transcription to produce an mRNA, followed by translation of the mRNA. Translation involves the conversion of the base sequence of the mRNA into the amino acid sequence of a polypeptide.
Hybridization between individuals from different species belonging to the same genus or two different genera, is termed as distant hybridization or wide hybridization, and such crosses are known as distant crosses or wide crosses.
The modes of reproduction in crop plants may be broadly grouped into two categories: asexual and sexual.
Sexual reproduction involves the fusion of male and female gametes, whereas in asexual reproduction new plants may develop from vegetative parts of the plant (vegetative reproduction) or may arise from embryos that develop without fertilization (apomixis).
The plant breeder frequently uses different tools/ instruments and materials to carry out selfing, artificial crossing and for taking field observations.
Multiple inbred founder lines are inter-mated for several generations prior to creating inbred lines, resulting in a diverse population whose genomes are fine scale mosaics of contributions from all founders.
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 .
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
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.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
(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.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
1. THE GENETIC MATERIAL
Prepared By:
Dr. Asit Prasad Dash
Assistant Professor
DEPARTMENT OF PLANT BREEDING AND GENETICS
INSTITUTE OF AGRICULTURAL SCIENCES
SIKSHA ‘O’ ANUSANDHAN (DEEMED TO BE UNIVERSITY), BHUBANESWAR,
751029
2. THE GENETIC MATERIAL:
It refers to the material of which genes are made.
Properties:
• High fidelity replication.
• Ability to express itself.
• Ability of store information.
• Must provide some error for origin of genetic variation.
IDENTIFICATION OF THE GENETIC MATERIAL
v The process of identification of genetic material began in 1928
with the experiments of Griffith and concluded in 1952 with the
studies of Hershey and Chase.
v Another ingenious experiment by Frankel-Conrat and Singer in
1957 established that in some viruses RNA functions as the
genetic material.
3. v But nuclic acids were discovered much earlier in 1871 by
Meischer who called them nuclein.
v There are two types of nucleic acids, viz., deoxyribose nucleic
acid (DNA) and ribose nucleic acid (RNA).
v In eukaryotes, chromosomes contain genes, and they are made
up of chromatin, i.e., DNA + proteins.
v Obviously, either DNA or protein would be the genetic material.
There was a prolonged controversy before DNA was
unequivocally accepted as the genetic material.
4. Experiment of Griffith
v Griffith discovered the phenomenon of transformation through
his studies on Diplococcus pneumoniae, which causes pneumonia
in most of the mammals.
v Different strains of Diplococcus form one of the following two
types of colonies: (1) smooth and (2) rough.
v The cells of strains forming smooth colonies are able to produce
pneumonia and are called virulent.
v But strains producing rough colonies are avirulent since they
cannot produce pneumonia.
v When live cells of the avirulent strain IIR (R is for rough
colonies) were injected into mice, all the mice survived as they did
not suffer from pneumonia.
v On the other hand, when mice were injected with live IIIS (S is for
smooth colonies; virulent) cells, all the mice died due to
pneumonia.
5.
6. v Further, mice injected with heat-killed cells of the virulent strain
IIIS did not develop pneumonia.
v However, when mice were injected with a mixture of heat-killed
IIIS cells and live IIR cells, some of them died due to pneumonia.
v Diplococcus cells isolated from the dead mice were of the type IIIS.
v Since all the cells of the heat-killed IIIS culture were dead, it was
postulated that some of the cells of IIR changed into the IIIS type
due to the influence of dead IIIS cells present in the mixture.
v This phenomenon was called transformation. The component of
IIIS cells, which induced the conversion of IIR cells into IIIS cells
was named as the transforming principle.
v The experiments of Griffith demonstrated transformation, but they
did not hint at the identity of the transforming principle. It was
later shown by Avery and co-workers that DNA is the
transforming principle.
7. Experiments of Avery,
MacLeod and McCarty
Avery and associates
carried out the
experiments of Griffith in
vitro on a glass vessel in
the place of mice (in
vivo).
8. Experiments of Hershey and Chase
v The results of these experiments, led to the universal acceptance
of DNA as the genetic material.
v Hershey and Chase studied the life cycle of T2 phage of E. coli;
they clearly showed that only the DNA component of T2 particles
is transmitted to the progeny phage particles.
v T2 and other bacteriophages are composed of protein and DNA.
v Head coat and tail are made up of protein, while the DNA is
packed inside the head coat.
v DNA contains phosphorus (P) but no sulphur (S), while
proteins contain S but no P.
v Therefore, they labelled T2 DNA with 32P, while proteins were
labelled with 35S.
9.
10.
11. RNA as Genetic Material
v In several viruses, e.g., TMV (tobacco mosaic virus), DNA is absent.
These viruses are composed of RNA and protein.
v TMV particles are like hollow cylinders. Their RNA is coiled like a
spring, while the protein molecules are arranged on the outside of the
coil.
v Frankel-Conrat and Singer demonstrated that RNA functions as
the genetic material in TMV.
v Proteins and RNA of TMV can be separated chemically; when
they are remixed under appropriate conditions, they reassociate to
produce active TMV particles.
v In one experiment, Frankel-Conrat and Singer used either RNA or
the proteins isolated from TMV for infection of tobacco leaves.
v Mosaic symptoms developed only when RNA was used for
infection (and not when the proteins were used).
v Clearly, only RNA fraction of TMV is capable of producing the
disease, and hence appears to be the genetic material.
12.
13. Components of DNA
Chemical analyses have shown that nucleic acids (DNA and RNA) are composed of
the following three types of molecules
1. Phosphoric Acid
Phosphoric acid (H3PO4) is involved in forming the sugar-phosphate backbone of
DNA, which is linked to the 5'C of one and the 3’C of the other neighbouring
pentose sugar molecule of DNA to produce the phosphodiester (5'C-0-P-0-C3')
linkage.
2. Pentose Sugar
The pentose present in RNA is called ribose from which this nucleic acid gets its
name. Similarly, DNA contains deoxyribose, which is the reason for the name
deoxyribose nucleic acid.
3. Organic Bases/ Nitrogenous bases
DNA ordinarily contains four different bases called, adenine (A), guanine (G),
cytosine (C) and thymine (T). RNA contains the same bases except for thymine
in it has uracil (U). These five bases (A, G, C, T, U) are grouped into two classes:
(I) pyrimidine (C, T, U) and (2) purine (A, G).
14.
15.
16. Nucleosides
Nucleosides are formed by the linkage of an organic base to the
pentose sugar with the help of a covalent bond.
Organic base + Ribose Riboside + 1H20
Organic base + Deoxyribose Deoxyriboside + 1H20
Ribosides and deoxyribosides = Nucleosides
Nucleotides
A Nucleotide is formed when a phosphate group is attached to the
pentose molecule of a nucleoside.
Organic base + Ribose + phosphate Ribotide + 2H20
Organic base + Deoxyribose + phosphate Deoxyribotide+ 2H20
Ribotides and deoxyribotides = Nucleotides
17.
18. PRIMARY STRUCTURE OF DNA
• A native DNA molecule is double-stranded.
• Each of the two strands of a DNA molecule has many deoxyribonucleotides, and
is known as a polynucleotide.
• These nucleotides are joined with each other by phosphodiester linkages.
• In a phosphodiester linkage, the 5'C of the pentose of one nucleotide is linked
with one -O- of the phosphate, while the 3'C of pentose of the other nucleotide
is linked with another -O- of the same phosphate residue. This produces a 5'C-
0-P-0-C3' linkage.
• Thus a polynucleotide chain consists of a backbone made-up of several alternating
pentose and phosphate molecules linked with each other; this is called sugar-
phosphate backbone.
• Each pentose has any one of the four organic bases.
• At one end of the polynucleotide chain, the 5'C of pentose has a free -OH (-OH of
the phosphate group attached to the 5'C), while the 3'C of the pentose at the
opposite end has a free -OH; these ends are known as 5'- and 3'-ends,
respectively.
19.
20. THE DNA DOUBLE HELIX
Chemical analyses of DNA by Chargaff to and others during 1940s
clearly demonstrated the following features. (Chargaff’s principle)
v The quantity of A is always equal to that of T, while the
quantity of G is equal to that of C.
v As a rule, the number of pyrimidine bases, i.e., C+T, is equal to
that of purine bases, viz., A + G.
v Similarly, A + C content of DNA is equivalent to that of G + T.
These findings were available by early 1950s, and were used by
Watson and Crick to develop the double helix model of DNA
formally proposed in 1953. This model was soon universally
accepted.
21. Main features of double helix model of DNA (Watson and Crick)
v A DNA molecule is made up of two polydeoxyribonucleotide (or simply
polynueleiotide) strands or chains.
v Each polynucleotide strand is composed of many deoxyribonucleotiries.
v The two strands of a DNA molecule are oriented antiparallel to each
other. This antiparallel orientation of the two strands is essential for the
formation of hydrogen bonds between the pairs of DNA bases
v The base sequences of the two strands of a DNA molecule show the
following universal relationship.
(a) Wherever adenine occurs in one strand, thymine is present in the
corresponding position of the other strand and vice-versa.
(b) the sites at which guanine is present in one strand are occupied
by cytosine in the second strand and vice-versa.
v Therefore, the two strands of a DNA molecule are called complementary
strands. Thus, if the base sequence of one strand of DNA is known, the
base sequence of its complementary stand can be easily deduced.
22. v The adenine present in one strand of a DNA molecule is linked by two hydrogen
bonds with the thymine located opposite to it in the second strand, and vice-versa.
v Similarly, G located in one strand forms three hydrogen bonds with the C present
opposite to it in the second strand and vice-versa.
v The two strands of a DNA molecule are coiled together in a right-handed helix
forming the DNA double helix.
v The diameter of this helix is 20 Å, while its pitch (length of helix required to
complete one turn) is 34 Å.
v In each DNA strand, the bases occur at a regular interval of 3.4 Å so that about 10
base pairs are present in one pitch of a DNA double helix. The base pairs in a
DNA molecule are stacked between sugar phosphate backbones of the two strands.
v During replication, the two strands of a DNA molecule uncoil. The unpaired bases
in the single-stranded regions of the two strands pair with their complementary
bases. These nucleotides become joined with each other and yield the
complementary strands of the old ones. This provides for an almost error-free
replication of the genetic material.
v Sometimes, errors in base-pairing may occur during replication. This would
account for the occurrence of mutations.
23.
24. THE A, B, C AND Z FORMS OF DNA
The above description is of the B-from of DNA. DNA is also known
to occur in three other forms (Table 1).
TABLE 1: Main differences between different forms of DNAs
Characteristic A-DNA B-DNA C-DNA Z-DNA
Coiling Right-
handed
Right-
handed
Right-
handed
Left-handed
Pitch 28 Å 34 Å 31 Å 69 Å
Base pairs per turn 11 10 9.33 12
Diameter 23 Å 19 Å 19 Å 18 Å
Vertical rise per
base pair
2.56 Å 3.38 Å 3.32 Å 5.71 Å
Sugar-phosphate
backbone
Regular Regular Regular Zig-zag
25. STRUCTURE OF RNA MOLECULES
v RNA, like DNA, is a polynucleotide.
v It is produced by phosphodiester linkages between
ribonucleotides in the same manner as in the case of DNA.
v RNA nucleotides have ribose sugar (in place of deoxyribose in
DNA), which participates in the formation of sugar-phosphate
backbone of RNA.
v Thymine is usually absent in RNA, and uracil is found in its place.
26. COMPARISON BETWEEN DNAAND RNA
Characteristics DNA RNA
Pentose sugar Deoxyribose Ribose
Organic base Ordinarily, thymine present
and uracil absent
Ordinarily, uracil present and
thymine absent.
Number of
strands
Generally, double-stranded Generally, single-stranded
Function Genetic material only (i) Generally, nongenetic functions,
e.g., mRNA rRNA, tRNA, etc.
(ii) In some viruses, genetic
material
Origin (i) Replication of pre-existing
DNA (ii) In case of infection
by RNA viruses, reverse
transcription of genetic RNA
(i) Transcription of DNA, or
(ii) Through replication of RNA by
RNA-dependent RNA polymerase
Native form Double-stranded DNA usually
in B-form
Double-stranded RNA usually in
A-form