Early Research: DNA's discovery has historical roots in genetics and scientific collaboration.
Key Figures: James Watson, Francis Crick, and Rosalind Franklin are notable contributors to the understanding of DNA's structure.
Configuration: DNA is composed of two antiparallel sugar-phosphate backbones with nitrogenous bases paired in the interior.
Base Pairing: Adenine pairs with Thymine (A-T), while Guanine pairs with Cytosine (G-C).
Double Helix: Watson and Crick developed the double helical model of DNA.
Mechanism: DNA replication is described as semi-conservative, meaning each new DNA molecule consists of one old and one new strand.
Key Enzymes:
DNA Polymerases: crucial for synthesizing new DNA strands and involved in repair processes.
Helicase: unwinds the DNA.
Primase: synthesizes RNA primers.
Ligase: seals nicks in the DNA backbone.
Prokaryotic vs. Eukaryotic:
Prokaryotes have a single origin of replication; Eukaryotes have multiple.
Speed: Prokaryotes replicate DNA at approx. 1000 nucleotides/sec; Eukaryotes at 50-100 nucleotides/sec.
Overview: An international scientific project that began in 1990 and was declared completed in April 2003, with about 92% of the human genome sequenced.
Purpose: Goals included sequencing all the nucleotides in human DNA and identifying all genes.
Levels of Packaging:
Nucleosomes: DNA wrapped around histones, forming a bead-like structure.
Chromatin: further coiling of nucleosomes into higher-order structures.
Metaphase Chromosome: highly condensed state observed just before cell division.
Types of Chromatin:
Euchromatin: loosely packed; often expressed.
Heterochromatin: densely packed; generally not expressed.
Definition: Structures that contain DNA and protein, found in the nucleus of eukaryotic cells.
Types:
Autosomes: all chromosomes except sex chromosomes.
Sex Chromosomes: determine biological sex, represented by X and Y (XX = female; XY = male).
Ploidy:
Diploid (2n): cells with pairs of homologous chromosomes (e.g., human somatic cells).
Haploid (1n): cells with a single set of chromosomes (e.g., human gametes).
Importance: To ensure the integrity of the genetic material by correcting any errors that occur during replication.
Mechanisms:
DNA Proofreading: performed by DNA polymerases which check and replace incorrect nucleotides.
Nucleotide Excision Repair: removes bulky lesions and corrects mismatches.
Error Types:
Point Mutations: changes at a single nucleotide.
Frameshift Mutations: insertions or deletions that change reading frame.
Chromosomal Mutations: larger-scale changes to chromosome structure.