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DNA-DNA hybridisation
combine strands of DNA at high temperatures
the higher the temperature the stronger the hydrogen bonding and the closer related the DNA strands are
mitochondrial DNA
mutates faster than nuclear DNA
no repair enzymes
slowly degrades after death
D-loop
hypervariable segment in mtDNA
RFLPs
restriction fragment length polymorphisms, the length can be used to group people by haplotypes into haplogroups
HVR1 and HVR2
control region includes 2 hyper variable regions that mutate faster and by sequencing them you ca define a person’s mitochondrial haplotype
mitochondrial “Eve”
root of mtDNA in Africa 200,000 years ago
there was not a single Eve and African populations are more diverse than non-African
Y chromosome
mtDNA is tracked to be much younger of an African origin, no recombination
difference between human and ape genomes
98.8% similar, differ in the dosage / regulation of identical genes
FOXP2
language gene
human accelerated regions (HARs)
region in the genome where the human lineage shows the highest number of changes
HAR1
most dramatically accelerated HAR, active in developing humans and expressed in testes
VLDLR gene
(very low density lipoprotein receptor) Turkish family who walk on all fours have a missense mutation in this gene causing disorder with cerebellar dysfunction and gait
other gene candidates for bipedality
genes of HOX family and the loss of GDF6 (opposable toe) growth differentiation factor 6
Recent African Origin Model
modern humans arose in Africa 100,000 years ago and spread throughout the world completely replacing other archaic human populations with no interbreeding
(African) Hybridisation and Replacement Model
humans spread from Africa and interbred with the other populations eventually replacing them
Assimilation Model
arose in Africa and migrated out, interbred extensively leading to genetic mixing rather than complete replacement
Multiregional Evolution Model
denies African origin and emphasises genetic continuity and gene flow between continents