Rovio Anja T, Abel Josef, Ahola Arja L, Andres Aida M, Bertranpetit Jaume, Blancher Antoine, Bontrop Ronald E, Chemnick Leona G, Cooke Howard J, Cummins James M, Davis Heidi A, Elliott David J, Fritsche Ellen, Hargreave Timothy B, Hoffman Susan M G, Jequier Anne M, Kao Shu-Huei, Kim Heui-Soo, Marchington David R, Mehmet Denise, Otting Nel, Poulton Joanna, Ryder Oliver A, Schuppe Hans-Christian, Takenaka Osamu, Wei Yau-Huei, Wichmann Lars, Jacobs Howard T
Institute of Medical Technology and Tampere University Hospital, University of Tampere, FIN-33014, Finland.
Mamm Genome. 2004 Jun;15(6):492-502. doi: 10.1007/s00335-004-3049-x.
The human nuclear gene for the catalytic subunit of mitochondrial DNA polymerase gamma ( POLG) contains within its coding region a CAG microsatellite encoding a polyglutamine repeat. Previous studies demonstrated an association between length variation at this repeat and male infertility, suggesting a mechanism whereby the prevalent (CAG)(10) allele, which occurs at a frequency of >80% in different populations, could be maintained by selection. Sequence analysis of the POLG CAG microsatellite region of more than 1000 human chromosomes reveals that virtually all allelic variation at the locus is accounted for by length variation of the CAG repeat. Analysis of POLG from African great apes shows that a prevalent length allele is present in each species, although its exact length is species-specific. In common chimpanzee ( Pan troglodytes) a number of different sequence variants contribute to the prevalent length allele, strongly supporting the idea that the length of the POLG microsatellite region, rather than its exact nucleotide or amino acid sequence, is what is maintained. Analysis of POLG in other primates indicates that the repeat has expanded from a shorter, glutamine-rich sequence, present in the common ancestor of Old and New World monkeys.
线粒体DNA聚合酶γ(POLG)催化亚基的人类核基因在其编码区域内含有一个编码聚谷氨酰胺重复序列的CAG微卫星。先前的研究表明,该重复序列长度变异与男性不育之间存在关联,这提示了一种机制,通过这种机制,在不同人群中出现频率>80%的常见(CAG)(10)等位基因可能通过选择得以维持。对1000多条人类染色体的POLG CAG微卫星区域进行序列分析发现,该位点几乎所有的等位基因变异都由CAG重复序列的长度变异所导致。对非洲大型猿类的POLG分析表明,每个物种中都存在一个常见的长度等位基因,尽管其确切长度具有物种特异性。在普通黑猩猩(Pan troglodytes)中,一些不同的序列变异促成了常见的长度等位基因,这有力地支持了这样一种观点,即维持的是POLG微卫星区域的长度,而非其确切的核苷酸或氨基酸序列。对其他灵长类动物的POLG分析表明,该重复序列是从旧世界猴和新世界猴的共同祖先中存在的较短的富含谷氨酰胺的序列扩展而来的。