In:
Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 100, No. 14 ( 2003-07-08), p. 8331-8336
Kurzfassung:
The study of genomic divergence between humans and primates may provide
insight into the origins of human beings and the genetic basis of unique human traits and diseases. Chromosome 21 is the smallest chromosome in the human
genome, and some of its regions have been implicated in mental retardation and other diseases. In this study, we sequenced the coding and regulatory regions
of 127 known genes on human chromosome 21 in DNA samples from human and chimpanzees and a part of the corresponding genes from orangutan, gorilla, and
macaque. Overall, 3,003 nucleotide differences between human and chimpanzee were identified over ≈400 kb. The differences in coding, promoter, and
exon–intron junction regions were 0.51 ± 0.02%, 0.88 ± 0.03%, and 0.85 ± 0.02%, respectively, much lower than the previously
reported 1.23% in genomic regions, which suggests the presence of purifying selection. Significant variation in substitution rate among genes was observed
by comparing the divergence between human and chimpanzee. Furthermore, by implementing a bioinformatics-based approach, we showed that the
identification of genetic variants specific to the human lineage might lead to an understanding of the mechanisms that are attributable to the phenotypes
that unique to humans, by changing the structure and/or dosage of the proteins expressed. A phylogenetic analysis unambiguously confirms the conclusion that
chimpanzees were our closest relatives to the exclusion of other primates and the relative divergence of the Homo – Pan and that of
( Homo – Pan )– Gorilla are 4.93 million
years and 7.26 million years, respectively.
Materialart:
Online-Ressource
ISSN:
0027-8424
,
1091-6490
DOI:
10.1073/pnas.1332748100
Sprache:
Englisch
Verlag:
Proceedings of the National Academy of Sciences
Publikationsdatum:
2003
ZDB Id:
209104-5
ZDB Id:
1461794-8
SSG:
11
SSG:
12
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