1] deCODE Genetics/Amgen, Inc., Reykjavik, Iceland. [2] Department of Anthropology, University of Iceland, Reykjavik, Iceland.
deCODE Genetics/Amgen, Inc., Reykjavik, Iceland.
Nat Genet. 2015 May;47(5):453-7. doi: 10.1038/ng.3171. Epub 2015 Mar 25.
Mutations are the fundamental source of biological variation, and their rate is a crucial parameter for evolutionary and medical studies. Here we used whole-genome sequence data from 753 Icelandic males, grouped into 274 patrilines, to estimate the point mutation rate for 21.3 Mb of male-specific Y chromosome (MSY) sequence, on the basis of 1,365 meioses (47,123 years). The combined mutation rate for 15.2 Mb of X-degenerate (XDG), X-transposed (XTR) and ampliconic excluding palindromes (rAMP) sequence was 8.71 × 10(-10) mutations per position per year (PPPY). We observed a lower rate (P = 0.04) of 7.37 × 10(-10) PPPY for 6.1 Mb of sequence from palindromes (PAL), which was not statistically different from the rate of 7.2 × 10(-10) PPPY for paternally transmitted autosomes. We postulate that the difference between PAL and the other MSY regions may provide an indication of the rate at which nascent autosomal and PAL de novo mutations are repaired as a result of gene conversion.
突变是生物变异的根本来源,其速率是进化和医学研究的关键参数。在这里,我们使用了来自 753 名冰岛男性的全基因组序列数据,这些男性分为 274 个父系谱系,根据 1365 次减数分裂(47123 年),估算了 21.3Mb 的男性特异性 Y 染色体(MSY)序列的点突变率。15.2Mb 的 X 退化(XDG)、X 转位(XTR)和非回文重复扩增子(rAMP)序列的综合突变率为 8.71×10(-10)个突变/位置/年(PPPY)。我们观察到来自回文序列(PAL)的 6.1Mb 序列的速率较低(P=0.04),为 7.37×10(-10) PPPY,与父系染色体的 7.2×10(-10) PPPY 速率没有统计学差异。我们假设 PAL 和其他 MSY 区域之间的差异可能表明新生常染色体和 PAL 新生突变由于基因转换而被修复的速率。