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25 Cards in this Set

  • Front
  • Back
genome
all of the DNA in a nucleus of a cell; humans have a lot of foreign DNA scattered throughout the genome, including transposons...as cellular DNA amounts increase there is a correlation in an increase in cell complexity and cell size
genome evolution
differences in species generation times lead to different rate of evolution
genes and gene families
many highly conserved during evolution; others are unique to each species
looking at conserved sequences allow.
comparison of two species and offers information about genetic basis of human diseases.
human vs/ tiger pufferfish
- last common ancestor 450 mya
- overall, the pufferfish genome has less DNA than the human genome
- 25% human genes have no counterpart in pufferfish
- repetitive DNA: 97% in humans, less than 16% in pufferfish but gene rearranging has been extensive in the genomes of the two vertebrates
- genes regulating the basic cellular metabolism are conserved in both species
human vs/ mouse
- human has 400 million more nucleotides but have about the same number of genes
- share a common ancestor more recently than humans with pufferfish
- share about 99% of genes
- 300 genes unique to either (only 1%)
- conservation of genes has been great in both genomes
- mouse genome has experienced a greater rate (2x) of chromosomal rearrangements than humans have
human vs/ chimp
- diverged 4.1 mya
- estimated genome sizes and number of genes is very similar in humans and chimpanzees
- less than 1% difference in protein coding genes confirms that humans and chimps are sibling species
- some insertion-deletions (indels) lead to loss of function changes in the two genomes
- mutations have led to major differences in gene expression
synteny
conserved arrangement of segments of DNA in related genomes which can be seen when linear order of genes is preserved over long sequences with a chromosome
polyploidy
caused when an entire genome duplicates in one species or from hybridization of two different species so that 3 or more complete copies of the genome exist in each cell
allopolyploids
results from hybridization and subsequent duplication of the genomes of two different species
duplicate genes
- can share the ancestral function of the original gene but usually do not share the same pattern of gene expression
- can lose their ancestral function and/or gain a derived function through subsequent mutation
- duplication is most likely to occur in growth and development genes, immune system genes, and cell-surface receptor genes
Arabidopsis vs/ Oryza
- distant relatives but share 80% genes
- they each have very high copy numbers (slightly divergent copies of a gene), probably indicating episodes of polyploidy and/or segmental duplication
duplication of DNA segments
when gene duplicates, the most likely fates of the duplicate gene are
1. loosing function through subsequent mutation
2. gaining a novel function through subsequent mutation
3. having the total function of the ancestral gene partitioned into the two duplicates
genes controlling basic metabolism
least likely to be duplicated
loss of gene function
- evolutionary mechanism

Consider: 60% of human OR (olfactory receptor) genes are pseudogenes (sequences of DNA that are very similar to functional genes but do not produce a functional product)...this inactivation may be because we rely on other senses so selection pressure against loss of OR genes reduced.
vertical gene transfer (VGT)
genes are passed from generation to generation
horizontal gene transfer (HGT)
genes are transferred from one species to another; this infrequently happens but happened more frequently in the distant past
pseudogenes
DNA sequences similar to functional genes, but which appear not to produce functional products; often created by gene inactivation
paralogues
two genes within an organism that have arisen from the duplication of a single gene in an ancestor and may be pseudogenes or evolve new functions
orthologues
reflects conservation of a single gene from a common ancestor therefore are likely to have the same function
evolution of speech
- the protein coded by the FOXP2 gene differs by only two amino acids in humans and chimps
- the FOXP2 gene is involved in the control of the neuromuscular pathway leading to complex sound formation
- in humans a single point mutation in the FOXP2 gene impairs speech and grammar
- FOXP2 may be involved in songbird singing and mouse vocalization
Plasmodium falciparum
- P. falciparum has many genes with similar function clustered together on its chromosomes
- P. falciparum is difficult for the immune system to target because it "cloaks" itself inside of red blood cells
plasmodium apicoplast
chloroplast-like organelle inherited from chloroplast of an alga and found only in plasmodium and its relatives; site where 12% of its proteins produce fatty acids; may offer vulnerability
transposons
small segments of DNA that move from one part of the genome to another part
transposase
- recognizes inverted repeast
- cleaves at both ends of the transposable element
- carries the transposable element to a new site on the DNA
- cleaves the target DNA at staggered sites