dna structure, the bonds involved and it seperation
TRANSCRIPT
DNA STRUCTURE
Outline Terms used. Polarity Bonds present Proteins involved Properties of nucleosides and nucleotides Structure of DNA
Watson Crick model Types of DNA DNA sequencing
Terminologies…. Nitrogenous base.
Nitrogen containing. Free pyrimidines and purines are weakly basic
compounds and thus are called bases
Sugar 2-Deoxy D-ribose pentose sugar
Terminologies…. Nucleoside
nitrogenous (nitrogen-containing) base a pentose
Nucleoside with Purine base have suffix –sine Pyrimidine base have suffix –dine
Nucleotide nitrogenous (nitrogen-containing) base a pentose a phosphate
Nucleic acid Linear polymers of nucleotides
Introns Non-coding, intervening , silent areas
Exons Coding, expressed regions
Cistrons Unit of gene expression, biochemical counterpart of
gene Gene
A segment of a DNA molecule that contains the information required for the synthesis of a functional biological product, whether protein or RNA.
Bases involved
Why thymine in DNA???
Deoxyribonucleosides Adenine Deoxyribose Deoxy-
adenosine(d-adenosine)
Guanine Deoxyribose Deoxy-guanosine(d-guanosine)
Cytosine Deoxyribose Deoxy-cytidine(d-cytidine)
Thymine Deoxyribose Deoxy-thymidine(d-thymidine)
Polarity In DNA the base sequence is always written in
5I end to 3I end direction By definition, the 5 end lacks a nucleotide
at the 5 position and the 3 end lacks a nucleotide at the 3 position.
5I -OH and 3I- OH ends. The 5 to 3 orientation of a strand of nucleic
acid refers to the ends of the strand.
Bonds involved… N-9 of a purine or N-1 of a pyrimidine is
attached to C-1 of the sugar The base lies above the plane of sugar when
the structure is written in the standard orientation;
The configuration of the N-glycosidic linkage is β .
Bonds involved… The successive nucleotides of DNA covalently
linked through phosphate-group “bridges” 5-phosphate group of one nucleotide unit is
joined to the 3-hydroxyl group of the next nucleotide
3I- to 5I Phosphodiester linkage
Covalent backbones of nucleic acids consist of alternating phosphate and pentose residues,
Nitrogenous bases as side groups joined at regular intervals.
Linkages can be cleaved hydrolytically by chemicals or enzymatically by family of Nucleases.
Comments… The covalent backbone of DNA and RNA is
subject to slow, non-enzymatic hydrolysis of the phosphodiester bonds.
In the test tube, RNA is hydrolyzed rapidly under alkaline conditions but DNA is not.
Hydrogen bonds Involving the amino and carbonyl groups are
the most important mode of interaction between two complementary strands of nucleic acid.
Required for specificity of base pairing
Other bonds… The stacking also involves a combination of
van der Waals and dipole-dipole interactions between the bases.
Base stacking helps to minimize contact of the bases with water, and
Base -stacking interactions are very important in stabilizing the three dimensional structure of nucleic acids
Base stacking in DNA is also favored by the conformations of the relatively rigid five-membered rings of the backbone sugars.
The sugar rigidity affects both the single-stranded and the double-helical forms.
Properties of nucleosides and nucleotidesPhysical properties Charged phosphate groups provide
interaction. Electron delocalization among atoms in the
ring gives most of the bonds partial double-bond character.
Strong absorption at wavelengths near 260 nm.
Purines have higher molar extinction coefficient.
Structural propertiesSugar puckering Displacement of 2 and 3 carbon atom above
the plane of C1-O4-C4 By convention above is the direction in which
the base and C5I project from the ring and is termed the endo face of the pentose.
If C2 is above it is called C2 endo If C3 is above it is called C3 endo Orientation of glycosidic bond and the
distance of the phosphate bond changes. DNA: C2 endo and RNA C3 endo.
Anti- & Syn- conformation… Nucleosides are planar. Still free rotation of glycosidic bond is
possible. In purines
H8 above sugar- anti conformation H8 below and far with bulk og purine ring above
sugar- syn In pyrimidines in pyrimidines
H6 is above sugar- anti conformation O2 is above sugar- syn conformation
Comments… Purines favour anti conformation..
Interconvert between the two Guanine 5I nucleotides is always an exception
Favours syn conformation.Importance Defines the handedness of the DNA helix. Anti conformation- right handed helix Syn- conformation- left handed helix DNA having more of G will have left handed
helix
Handedness If you look up through
the bottom of a helix along the central axis and the helix spirals away from you in a clockwise direction it is a right-handed helix.
If it spirals away from you in a counter-clockwise direction, it is a left handed helix.
Proteins involved… Histones
Genes for histones seem to have no introns
Nucleosome Dna wraps twice around histone octamer
Nucleosome
Condensed Chromosome Structures AreMaintained by…. A third major class of chromatin proteins SMC
proteins (structural maintenance of chromosomes).
Proteins in the SMC family are found in all types of organisms, from bacteria to humans.
Eukaryotes have two major types, cohesins and condensins.
Cohesins linking together sister chromatids
Condensins – condensation of chromosomes as cells enter mitosis
DNA & its history… DNA is in nucleus.. Storage of inorganic phosphate.. It carries genetic information It is passed to daughter cell…
Then Experiments to elucidate the structure..
DNA helix in history…. DNA was first isolated and characterized by
Friedrich Miescher in 1868. He called the phosphorus-containing
substance “nuclein.” Alfred D. Hershey and Martha Chase, in which
they studied the infection of bacterial cells by a virus (bacteriophage) with radioactively labeled DNA or protein, removed any remaining doubt that DNA, not protein, carried the genetic information
1951—Rosalind Franklin—X-ray crystallography
Chargaff—Chargaff’s rules. Ratio of nitrogenous bases in DNA. Complimentary bases.
Watson & Crick--1953
Erwin Chargaff
Chargaff’s conclusions Base composition of DNA varies from one species to
another. DNA specimens isolated from different tissues of the
same species have the same base composition. The base composition of DNA in a given species does
not change with an organism’s age, nutritional state, or changing environment.
In all cellular DNAs, regardless of the species, Number of adenosine residues is equal to thymidine
residues (that Number of guanosine residues is equal to cytidine residues
Sum of the purine residues equals pyrimidine residues
Watson Crick model
Two helical polynucleotide chains are coiled around a common axis. The chains run in opposite directions.
The sugar-phosphate backbones are on the outside and, therefore,
Purine and pyrimidine bases lie on the inside of the helix.
The bases are nearly perpendicular to the helix axis, and adjacent bases are separated by 3.4 Å.
The helical structure repeats every 34 Å, so there are 10 bases (= 34 Å per repeat/3.4 Å per base) per turn of helix.
There is a rotation of 36 degrees per base (360 degrees per full turn/10 bases per turn).
The diameter of the helix is 20 Å. The complimentary nitrogenous bases form
hydrogen bonds between the strands. A is complimentary to T and G is
complimentary to C.
B- DNA, right handed, 10 base pairs per turn. Two chains coiled around a common axis:
Axis of symmetry. Pairs in an anti- parallel manner i.e. 5′- end
pairs with 3′- end of other strand. Phosphate molecules are hydrophillic,
whereas bases forms the hydrophobic molecules.
Spatial arrangement of two strands creates Major (wide) & minor (narrow) Groove.
Bases are perpendicular to axis, sugars are at right angle to those of bases.
Diameter of helix is 20nm, adjacent bases separated by 3.4Ǻ.
One complete turn of 10 BP occurs at interval of 34Ǻ.
Circular DNA molecules Each chromosome in the nucleus of a eukaryote
contains one long linear molecule of dsDNA. Eukaryotes have closed circular DNA molecules
in their mitochondria. A prokaryotic organism contains a single, double-
stranded, supercoiled, circular chromosome. Each prokaryotic chromosome is associated with
histone-like proteins and RNA that can condense the DNA to form a nucleoid.
Species of bacteria also contain small, circular, extrachromosomal DNA molecules called plasmids.
Other types of DNA Bent DNA
4-6 adenines separated by 10 bp. Minor grooves compressed Interaction with proteins & enzymes
Cruciform DNA Disruption of hydrogen bonds between
complimentary bp Formation of intra strand hydrogen bonds. Formation of hairpin
Other types of DNA Triple stranded DNA
Polynucleotides of Poly (dA) & poly (dT) Hoogsteen triple helix TAT, CGC triplet bp
Four stranded DNA Rich in guanine nucleotides. G-quartets. Guanine with hoogsteen hydrogen bonds. Existence invivo not proven
Slipped DNA Direct repeat symmetry Formation of two single stranded loops. Fragile X syndrome typical example of triple
repeat sequence. Frame shift mutation explained on this basis.
Triple stranded DNA
Melting temperature Temperature at which one half of the helical
structure is lost is defined as the melting temperature (Tm).
The loss of helical structure in DNA, called denaturation, can be monitored by measuring its absorbance at 260 nm
Ss DNA has a higher relative absorbance at this wavelength than does ds DNA.
Complementary DNA strands can reform the double helix by the process called renaturation (or reannealing).
Importance of Tm Critical importance in any technique that
relies on complementary base pairing Designing PCR primers Southern blots Northern blots Colony hybridization
Factors Affecting Tm G-C content of sample Presence of intercalating agents (anything
that disrupts H-bonds or base stacking) Salt concentration pH Length
DNA packaging
DNA Sequencing
1. Sanger dideoxynucleotide chain termination method
A. Manual method B. Automated method2. Chemical cleavage method (Maxam and
Gilbert method) Not used nowadaysUse of the technique Provides the order of the nucleotides in a
given DNA
Sanger Method
Partial copies of DNA fragments made with DNA polymerase
Collection of DNA fragments that terminate with A,C,G or T using ddNTP
Separate by gel electrophoresis Read DNA sequence
Requirements for Sanger Method DNA to be sequenced must be in single strand
form. The region to be sequenced must be 3I
flanked by known sequence. Reagents needed:
A primer complementary to the known region to start and direct chain synthesis. (15-30 nucleotides in length)
DNA polymerase. 4 deoxynucleotide triphosphates (dNTPs). 4 dideoxynucleotide triphosphates (ddNTPs)
Take home message… All life on earth use nucleic acid to store
genetic information. Except some viruses(RNA) it is stored in DNA. So why DNA??? Chemical stability.. Store vast genetic informationAnd most important!!!!!
Encode this vast genetic information with simple four letter code(A,G,C &T)
References.. Text Book Of Biochemistry With Clinical
Correlation By Thomas Devlin 7th Edition Lehninger Principles Of Biochemistry. 5th
Edition Lippincott's Illustrated Reviews: Biochemistry
4th Edition Stryer's Biochemistry- 5th edition Marks’ Basic Medical Biochemistry: A Clinical
Approach, 2nd Edition Textbook Of Biochemistry DM Vasudevan 6th
Edition