Slide 52
Fig. 21-10b
(b) The human -globin and -globin gene families
Heme
Hemoglobin
-Globin
-Globin
-Globin gene family
-Globin gene family
Chromosome 16
Chromosome 11
2
1
2
1
G
A
Embryo
Embryo
Fetus
Fetus
and adult
Adult
Slide 53
Concept 21.5: Duplication, rearrangement, and mutation of DNA contribute to genome evolution
The basis of change at the genomic level is mutation, which underlies much of genome evolution
The earliest forms of life likely had a minimal number of genes, including only those necessary for survival and reproduction
The size of genomes has increased over evolutionary time, with the extra genetic material providing raw material for gene diversification
Slide 54
Accidents in meiosis can lead to one or more extra sets of chromosomes, a condition known as polyploidy
The genes in one or more of the extra sets can diverge by accumulating mutations; these variations may persist if the organism carrying them survives and reproduces
Slide 55
Humans have 23 pairs of chromosomes, while chimpanzees have 24 pairs
Following the divergence of humans and chimpanzees from a common ancestor, two ancestral chromosomes fused in the human line
Duplications and inversions result from mistakes during meiotic recombination
Comparative analysis between chromosomes of humans and 7 mammalian species paints a hypothetical chromosomal evolutionary history
Slide 56
Fig. 21-11
Human chromosome 16
Blocks of DNA
sequence
Blocks of similar sequences in four mouse chromosomes:
7
8
16
17
Slide 57
The rate of duplications and inversions seems to have accelerated about 100 million years ago
This coincides with when large dinosaurs went extinct and mammals diversified
Chromosomal rearrangements are thought to contribute to the generation of new species
Some of the recombination “hot spots” associated with chromosomal rearrangement are also locations that are associated with diseases
Slide 58