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Y染色体微卫星突变率:基因座之间和基因座内部突变率的差异。

Y-chromosomal microsatellite mutation rates: differences in mutation rate between and within loci.

作者信息

Dupuy B Myhre, Stenersen M, Egeland T, Olaisen B

机构信息

Institute of Forensic Medicine, University of Oslo, Rikshospitalet, Oslo, Norway.

Biostatistics, Rikshospitalet, Oslo, Norway.

出版信息

Hum Mutat. 2004 Feb;23(2):117-124. doi: 10.1002/humu.10294.

Abstract

Precise estimates of mutation rates at Y-chromosomal microsatellite STR (short tandem repeat) loci make an important basis for paternity diagnostics and dating of Y chromosome lineage origins. There are indications of considerable locus mutation rate variability between (inter-) and within (intra-) loci. We have studied nine Y-STR loci-DYS19, DYS389I/II, DYS390, DYS391, DYS392, DYS393, DYS385, and DYS388-in 1,766 father-son pairs of confirmed paternity (a total of 15,894 meioses). Five biallelic markers were also analyzed in the fathers-Tat, YAP, 12f2, SRY1532, and 92R7-defining haplogroups 1, 2, 3, 4, 9, and 16, respectively. A total of 36 fragment length mutations were observed: 24 gains (22 single-step, two double-step) and 12 single-step losses. Thus, there was a significant surplus of gains (p=0.045). Overall, the mutation rate was positively correlated to STR repeat length and there was a significant relative excess of losses in long alleles and gains in short alleles (p=0.043). In contrast to the situation in autosomal STR loci and in MSY-1, no noteworthy correlation between mutation rate and the father's age at the child's birth was observed. We observed significant interlocus differences in Y-STR mutation rates (p<0.01). The number of observed mutations ranged from zero in DYS392 to eight in DYS391 and DYS390. We have also demonstrated obvious differences in mutation rates between the haplogroups studied (p=0.024), a phenomenon that is a reflection of the dependence of mutation rate on allele size. Our study has thus demonstrated the necessity of not only locus-specific, but even allele-specific, mutation rate estimates for forensic and population genetic purposes, and provides a considerable basis for such estimates.

摘要

精确估计Y染色体微卫星STR(短串联重复序列)位点的突变率是亲子鉴定和Y染色体谱系起源追溯的重要基础。有迹象表明,不同位点间(位点间)和同一位点内(位点内)的突变率存在显著差异。我们研究了1766对经确认父子关系的父子对中的9个Y-STR位点——DYS19、DYS389I/II、DYS390、DYS391、DYS392、DYS393、DYS385和DYS388(共15894次减数分裂)。还对父亲中的5个双等位基因标记——Tat、YAP、12f2、SRY1532和92R7进行了分析,它们分别定义单倍群1、2、3、4、9和16。共观察到36次片段长度突变:24次增加(22次单步、2次两步)和12次单步减少。因此,增加的数量显著过剩(p = 0.045)。总体而言,突变率与STR重复长度呈正相关,长等位基因的减少和短等位基因的增加存在显著的相对过剩(p = 0.043)。与常染色体STR位点和MSY-1的情况不同,未观察到突变率与孩子出生时父亲年龄之间的显著相关性。我们观察到Y-STR突变率存在显著的位点间差异(p < 0.01)。观察到的突变数量从DYS392中的零到DYS391和DYS390中的八不等。我们还证明了所研究的单倍群之间突变率存在明显差异(p = 0.024),这一现象反映了突变率对等位基因大小的依赖性。因此,我们的研究表明,出于法医和群体遗传学目的,不仅需要进行位点特异性的突变率估计,甚至需要进行等位基因特异性的突变率估计,并为此类估计提供了大量依据。

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