DNA Structure
Historical Context of DNA Discovery
Key Figures in DNA Research
James D. Watson and Francis H. Crick: Developed the double helix model of DNA in 1962, which earned them the Nobel Prize in Physiology and Medicine.
Rosalind Franklin: Her X-ray diffraction images of DNA were crucial in revealing its helical structure, although she did not receive the same recognition during her lifetime.
Maurice H. Wilkins: Collaborated with Franklin and Watson & Crick, contributing to the understanding of DNA's structure.
The Significance of the Double Helix Model
The double helix model proposed by Watson and Crick explained how genetic information is stored and replicated.
The model illustrated the complementary base pairing, which is fundamental for DNA replication and function.
Structure of DNA
Composition of DNA
DNA is a nucleic acid composed of nucleotides, which are the monomers of DNA.
Each nucleotide consists of three components: a phosphate group, a deoxyribose sugar, and a nitrogenous base.
Types of Nitrogenous Bases
Pyrimidines: Single-ring structures including Cytosine (C) and Thymine (T) (only in DNA).
Purines: Double-ring structures including Adenine (A) and Guanine (G).
Base pairing rules: A pairs with T (2 hydrogen bonds), and C pairs with G (3 hydrogen bonds).
DNA vs. RNA
DNA and RNA differ in several key aspects:
DNA is double-stranded, while RNA is single-stranded.
DNA contains deoxyribose sugar; RNA contains ribose sugar.
DNA has Thymine (T), whereas RNA has Uracil (U).
DNA Replication Process
Overview of DNA Replication
DNA replication is a semi-conservative process, meaning each new DNA molecule consists of one old strand and one new strand.
The process is initiated at origins of replication, where the double helix unwinds.
Enzymes Involved in DNA Replication
Helicase: Unwinds the DNA strands.
DNA Polymerase III: Adds nucleotides to the growing DNA strand and proofreads for errors.
DNA Polymerase I: Removes RNA primers and replaces them with DNA nucleotides.
Ligase: Joins Okazaki fragments on the lagging strand.
Leading vs. Lagging Strand Synthesis
The leading strand is synthesized continuously in the 5’ to 3’ direction.
The lagging strand is synthesized discontinuously, forming short segments called Okazaki fragments, which are later joined together.
DNA Repair Mechanisms
Proofreading and Error Correction
DNA polymerase has proofreading capabilities, correcting errors during replication at a rate of 1 in 10,000 bases.
Mismatch repair enzymes correct incorrectly paired bases after DNA synthesis.
Nucleotide Excision Repair
Nucleases cut out damaged DNA segments, which are then replaced by DNA polymerase and ligase.
Example: Xeroderma pigmentosum is a genetic disorder caused by mutations in DNA repair enzymes, leading to increased skin cancer risk.
Mutation Rates and Implications
Mutations can occur at a rate of 1 per 10,000 bases, with a higher cumulative effect due to the large human genome.
Each individual may inherit 3-4 mutations, which can contribute to genetic diversity and disease.