In genomic sequencing the sequence of nucleotide bases can be determined for individual genes and entire genomes
Many genomes have been sequenced, particularly of disease-causing organisms, pest species and species that are important model organisms for research
Genomes from different species are often compared
comparison of genomes reveals that many genes are highly conserved across different organisms
Bioinformatics is the use of computer analysis and statistical analysis to compare genomic sequence data
Computer programs can be used to identify base sequences similar to known genes
Phylogenetics is the study of the evolutionary relatedness among groups of organisms
Comparison of sequences provides evidence of the three domains of life- bacteria, archaea and eukaryotes
The data from genomic sequencing is used to work out the evolutionary history and relationships of different species
Species with more similarity in their genomes are more closely related
A phylogenetic tree can be read like a map of evolutionary history
The vertical lines, called branches represent the lineage
Phylogenetics can be used to work out:
lineage- the exact sequence in which species can be traced back through ancestral populations
sequencedivergence- how and when lineages diverged from common ancestry
A molecular clock is a measure of evolutionary change over time at the molecular level
Molecular clocks use sequence data to measure the number of mutations that accumulate in a DNA sequence over time to show when species diverged during evolution
Molecular clocks assume that DNA sequences and amino acid sequences mutate at a constant rate
Therefore, differences in sequence data between species indicate the time of divergence from a common ancestor
Evidence from phylogenectics and molecular clocks has been used to determine the main sequence of events in evolution
Sequence data (from phylogenetics), along with fossil evidence, has allowed biologists to determine the main sequence of events in the evolution of life.
cells
last universal ancestor
prokaryotes
photosynthetic organisms
eukaryotes
multicellular life
animals
verebrates
land plants
Medical researchers may use genomic information to compare the DNA of individuals who bear an inherited disease with those who are unaffected
Differences between their genomes may reveal the presise mutation and cause of their condition
An individual's genome can be analysed to predict the likelihood of developing certain diseases
Pharmacogenetics is the use of genome information in the choice of drugs
An individual's personal genome sequence can be used to select the most effective drugs and dosage to treat their disease.