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人类和黑猩猩的微卫星等位基因频率及其对等位基因大小限制的影响

Microsatellite allele frequencies in humans and chimpanzees, with implications for constraints on allele size.

作者信息

Garza J C, Slatkin M, Freimer N B

机构信息

Department of Integrative Biology, University of California, Berkeley 94720, USA.

出版信息

Mol Biol Evol. 1995 Jul;12(4):594-603. doi: 10.1093/oxfordjournals.molbev.a040239.

Abstract

The distributions of allele sizes at eight simple-sequence repeat (SSR) or microsatellite loci in chimpanzees are found and compared with the distributions previously obtained from several human populations. At several loci, the differences in average allele size between chimpanzees and humans are sufficiently small that there might be a constraint on the evolution of average allele size. Furthermore, a model that allows for a bias in the mutation process shows that for some loci a weak bias can account for the observations. Several alleles at one of the loci (Mfd 59) were sequenced. Differences between alleles of different lengths were found to be more complex than previously assumed. An 8-base-pair deletion was present in the nonvariable region of the chimpanzee locus. This locus contains a previously unrecognized repeated region, which is imperfect in humans and perfect in chimpanzees. The apparently greater opportunity for mutation conferred by the two perfect repeat regions in chimpanzees is reflected in the higher variance in repeat number at Mfd 59 in chimpanzees than in humans. These data indicate that interspecific differences in allele length are not always attributable to simple changes in the number of repeats.

摘要

研究发现了黑猩猩八个简单序列重复(SSR)或微卫星位点的等位基因大小分布,并将其与之前从几个人类群体中获得的分布进行比较。在几个位点上,黑猩猩和人类之间平均等位基因大小的差异足够小,以至于平均等位基因大小的进化可能存在限制。此外,一个考虑到突变过程中偏差的模型表明,对于某些位点,微弱的偏差可以解释这些观察结果。对其中一个位点(Mfd 59)的几个等位基因进行了测序。发现不同长度等位基因之间的差异比之前假设的更为复杂。在黑猩猩位点的非可变区域存在一个8个碱基对的缺失。该位点包含一个以前未被识别的重复区域,在人类中是不完美的,而在黑猩猩中是完美的。黑猩猩中两个完美重复区域赋予的明显更大的突变机会,反映在黑猩猩中Mfd 59位点重复数的方差高于人类。这些数据表明,等位基因长度的种间差异并不总是归因于重复数目的简单变化。

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