Ch 9 - How Genes and Genomes Evolve Flashcards
Alu sequence
family of mobile genetic elements that comprises about 10% of the human genome; this short, repetitive sequence is no longer mobile on its own, but requires enzymes encoded by other elements to transpose
conserved synteny
the preservation of gene order in the genomes of different species
exon shuffling
mechanism for the evolution of new genes; in the process, coding sequences from different genes are brought together to generate a protein with a new combination of domains
gamete
cell type in a diploid organism that carries only one set of chromosomes and is specialized for sexual reproduction. a sperm or an egg; also called a germ cell
gene duplication and divergence
a process by which new genes can form; involves the accidental generation of an additional copy of a stretch of DNA containing one or more genes, followed by an accumulation of mutations that over time can alter the function or expression of either the original or its copy
gene family
a set of related genes that has arisen through a process of gene duplication and divergence
germ line
the lineage of reproductive cells that contributes to the formation of a new generation of organisms, as distinct from somatic cells, which form the body and leave no descendants in the next generation
homologous gene
describes genes, chromosomes or any structures that are similar because of their common evolutionary origin. can also refer to similarities between protein sequences or nucleic acid sequences
horizontal gene transfer
process by which DNA is passed from the genome of one organism to that of another, even to an individual from another species. this contrasts with ‘vertical gene transfer’, which refers to the transfer of genetic information from parent to progeny
L1 element
type of retrotransposon that constitutes 15% of the human genome; also called LINE-1
mobile genetic element
short segment of DNA that can move, sometimes through an RNA intermediate, from one location in a genome to another; an important source of genetic variation in most genomes. also called a transposon
open reading frame (ORF)
long sequence of nucleotides that contains no stop codon; used to identify potential protein-coding sequences in DNA
phylogenetic tree
diagram or ‘family tree’ showing the evolutionary relationships among groups of organisms or proteins
point mutation
change in a single nucleotide pair in a DNA sequence
purifying selection
preservation of a specific nucleotide sequence by the elimination of individuals carrying mutations that interfere with its functions