DNA: Consists of two strands that form a double helix structure, Each DNA strand is composed of nucleotides, The sequences of nitrogenous bases on the two strands are complementary, The nitrogenous base pairs are joined by hydrogen bonds, The two strands of DNA are antiparallel
RNA: Uses the sugar ribose instead of deoxyribose, Generally single-stranded, Contains uracil in place of thymine
Central Dogma of Molecular Biology: DNA contains the complete genetic information that defines the structure and function of an organism, Proteins are formed using the genetic code of the DNA, Conversion of DNA encoded information to RNA is essential to form proteins
DNA replication: Semi-conservative mode, Resulting daughter molecules each have one parental (old) strand and one newly synthesized strand, Watson and Crick base pairing maintained, DNA is synthesized in the 5' to 3' method, A primer is needed for initiation
Stages of Replication: Initiation:Origin of Replication - sequence of DNA at which replication is initiated, DNA gyrase and topoisomerases relaxes supercoiling ahead of the replication fork, Replication fork - the point at which replication actively occurs, The two strands of parental DNA are unwound by helicase, Primers - signal the starting point of DNA replication, synthesized by primase
Stages of Replication: Elongation: Leading strand - continuous, one primer, DNA polymerase, 5' to 3', Lagging strand - synthesized opposite to the fork movement, discontinuous, several primers, DNA polymerase, 5' to 3', Okazaki fragments
Stages of Replication: Termination: Forks converge until all intervening DNA is unwound, Any remaining gaps are filled and ligated (DNA ligase), Replication proteins are unloaded
Transcription: RNA polymerase binds to the DNA at a site called the promoter, RNA polymerase synthesize mRNA in the 5' - 3' direction, RNA synthesis continues until RNA polymerase reaches a site on the DNA called the terminator
Translation: Also known as protein synthesis, The language of mRNA is in the form of codons (groups of 3 nucleotides), The sequence of codons on an mRNA molecule determines the sequence of amino acids that will be in the protein being synthesized
Genetic Code: There are 61 possible codons but only 20 amino acids, Third Base Degeneracy or Wobble Hypothesis states that codons for same amino acid usually differ in 3rd position only
Steps in Translation: The ribosome binds to mRNA at a specific area, The ribosome starts matching tRNA anticodon sequences to the mRNA codon sequence, Each time a new tRNA comes into the ribosome, the amino acid that it was carrying gets added to the elongating polypeptide chain, The ribosome continues until it hits a stop sequence, then it releases the polypeptide and the mRNA, The polypeptide forms into its native shape and starts acting as a functional protein in the cell
Mutation: Any heritable alteration in the base sequence of the genetic material, Can either be spontaneous or induced
Types of Mutation: Base Substitution (point mutation or base pair changes), Transition (purine to purine or pyrimidine to pyrimidine), Transversion (purine to pyrimidine)
Mutation is the initial and final states of the organisms
When established, mutation may be permanently present whether or not the conditions of development of the mutated organism allow their detection
Mutation it can either be spontaneous or induced
Spontaneous mutation is occurs without external intervention, and most result from occasional errors in the pairing of bases by DNA polymerase during DNA replication
Induced mutation: Caused by agents in the environment and include mutations made deliberately by humans, Results from exposure to natural radiation that alters the structure of bases in the DNA, or from a variety of chemicals that chemically modify DNA
Base Substitution: Also called as point mutation or base pair changes, A single base at one point in the DNA sequence is replaced with a different base during replication, Can either be (1) transition – purine to purine (A→G) or pyrimidine to pyrimidine (C→T) – or (2) transversion – purine to pyrimidine or vice versa
Consequences of Base Substitutions: Missense mutation, Nonsense mutation, Silent mutation
Missense mutation: Changes a codon for one amino acid to a codon for another amino acid, Results in an amino acid substitution in the protein product
Nonsense mutation it changes a codon for an amino acid with a codon for chain termination (UAG, UAA, UGA)
Silent mutation is a change in codon composition that has no effect on the resulting polypeptide
Frameshift mutation: Adds or deletes one or two bases (or any non-multiple of 3) from a coding sequence in a DNA, so that the genetic code is read out-of-phase, Consequences: (a) incorrect amino acid or premature termination and/or (b) severe phenotypic effects
Deletion is a mutation in which a region of the DNA has been eliminated
Insertion it occurs when new bases are added to the DNA
Mutagens is physical or chemical agents that changes the genetic material
Electromagnetic radiations: Gamma rays, X-rays and ultraviolet rays, Penetration power is inversely proportional to their wavelength
Ionizing radiations (Gamma rays and X-rays): Direct effect: Single or double-stranded breaks in the DNA molecules, Indirect effect: Free radicals created; form compounds, HO2 – initiate harmful chemical reactions within the cells; can lead to cell death
Non-ionizing radiations (UV rays) is formation of pyrimidine dimers – most are immediately repaired, but some escape repair and inhibit replication and transcription
Particulate Radiations: Are in the form of sub-atomic particles emitted from the atoms with high energy, Penetrating power: Beta particles > alpha particles because of its smaller size, Neutrons: extremely penetrant, and can cause severe damage to the living tissues as well as genetic material, Result: Single strand or double strands break in the DNA
Chemical Mutagens: Deaminating agents, Base Analogs, Alkylating Agents, Intercalating Agents
Deaminating agents it cause the loss of the amino group. Examples are nitric oxide, nitrous acid and N-nitrosoindoles
Base Analogs: Structurally resemble purines and pyrimidines and may be incorporated into DNA in place of the normal bases during DNA replication, They induce mutations because they often have different base-pairing rules than the bases they replace