Diversity in genome sizes:
Ranges from small viruses to larger eukaryotes (e.g., flowering plants, mammals).
Genome size is measured in Megabases (Mb).
Species and their Genome Size:
Examples include:
Viruses (e.g., Bacteriophage) with small genomes.
Bacteria like E. coli have compact genomes.
Eukaryotes (e.g., mammals, plants) exhibit larger genome sizes owing to different factors.
Historical Costs:
First human genome sequence cost approximately $3 billion.
As of today, costs have reduced to below $5,000.
Completed Species Genomes:
As of 2014, over 500 eukaryotic and 17,000 prokaryotic genomes were sequenced.
Differences arise primarily due to:
Non-coding DNA: Much of the genome may not code for proteins.
Cell volume: Larger nuclei may facilitate larger genomes.
Transposons: Movements of genetic material within genomes contribute to size variations.
Gene Complexity:
Number of genes is not the sole determinant of phenotype complexity.
Gene regulatory networks vary among organisms and affect phenotypes.
Non-coding regions can play significant regulatory roles.
Alternative splicing allows one gene to code for multiple proteins.
Viruses:
SARS Coronavirus RNA: Approximately 21,485 bp with key proteins (Spike (S), Nucleocapsid (N), etc.).
Hepatitis B DNA: Contains multiple surface proteins and a polymerase gene.
Bacterial Genome (E. coli):
Contains various features influencing pathogenicity such as virulence factors and toxin production.
Methods:
Transduction: Transfer of DNA via bacteriophages.
Transformation: Uptake of environmental DNA.
Conjugation: Transfer of plasmid DNA from one bacterium to another.
Implications: Enables rapid genetic variations and adaptations.
Human Genome Composition:
Protein-coding genes: ~1.5%.
Non-coding regions including introns and transposable elements (50% of human genome).
Mitochondrial Genome:
Significant as it reflects a separate lineage due to endosymbiosis.
Mechanisms include:
Descent with Modification: Changes in genomes over time.
Duplication Events: Lead to gene families and functional variability.
Retrotransportation: mRNA converted back to DNA, creating duplicates without introns.
Pseudogenes: Non-functional duplicates resulting from mutations.
Introgression: Mixing of alleles between species; significant in evolutionary history (e.g., Neanderthal genes in Homo sapiens).
Incomplete Lineage Sorting: Can lead to incorrect phylogenetic inferences if based on single genes.
Using whole genomes can clarify evolutionary relationships better than single genes.
Out-of-Africa Model: Supported by phylogenetic data reflecting human development and migration patterns.
Exons: Coding regions of DNA.
Introns: Non-coding segments spliced out before protein synthesis.
Transposable Elements: Mobile genetic elements influencing genome structure and evolution.