Genetics: Study of genes, how they carry information, their expression, and replication.
Gene: Segment of DNA encoding a functional product, typically protein.
Chromosome: Structure containing DNA that carries hereditary information; contains genes.
Genome: Complete genetic content of a cell.
Genomics: Molecular study of genomes.
Genotype: The genetic makeup of an organism.
Phenotype: Observable expression of genes.
Image Reference 8.1a: Depicts a disrupted E. coli cell's chromosome structure.
Image Reference 8.1b: Genetic map of E. coli's chromosome showcasing various metabolic functions and processes.
Figure 8.2: Overview of how genetic information within a cell is expressed to produce necessary proteins, involving processes of transcription and translation, including cell metabolism and growth.
Composition: DNA is a polymer of nucleotides (adenine, thymine, cytosine, guanine).
Structure: Double helix with a deoxyribose-phosphate backbone; strands held together by hydrogen bonds between AT/CG pairs.
Strand Orientation: Strands are antiparallel and complementary.
Definition: DNA is transcribed to produce RNA (mRNA, tRNA, rRNA).
Steps:
Initiation: RNA polymerase binds to the promoter sequence.
Elongation: RNA strand is synthesized in the 5' to 3' direction.
Termination: Process ends at the terminator sequence.
Figure 8.7: Shows RNA polymerase action from initiation to termination.
Mechanism: mRNA is translated at ribosomes into proteins by tRNA carrying amino acids via codons.
Key Points:
Begins at start codon (AUG), stops at nonsense codons (UAA, UAG, UGA).
The genetic code includes 64 codons for 20 amino acids, demonstrating degeneracy.
Figures 8.9 and 8.10: Illustrate the sequential steps of translation from initiation, peptide bond formation, to termination.
Definition: Changes in genetic material that can be neutral, beneficial, or harmful.
Types:
Spontaneous mutations: Occurs without mutagens.
Missense mutation: Alters one base, changing amino acid.
Nonsense mutation: Produces a stop codon due to base substitution.
Frameshift mutation: Caused by insertions or deletions that disrupt reading frames.
Detection: Via experiments like the Ames test which evaluates mutagenic potential.
Gene Transfer Methods:
Vertical Gene Transfer: Transmission during reproduction between generations.
Horizontal Gene Transfer: Transfer of genes between cells of the same generation, includes transformation, transduction, and conjugation.
Figures 8.24-8.29: Illustrate crossing over, transformation via naked DNA, and conjugation mechanism.
Plasmids: Circular DNA that can replicate independently; carry genes such as antibiotic resistance (0 R factors).
Transposons: DNA segments that can move within the genome, facilitating genetic variation.
Types of Transposons: Insertion sequences (simplest), complex ones carrying additional genes.
Role in Evolution: Mutations and recombination increase diversity, providing material for natural selection, influencing organism adaptation.