Carroll M L, Roy-Engel A M, Nguyen S V, Salem A H, Vogel E, Vincent B, Myers J, Ahmad Z, Nguyen L, Sammarco M, Watkins W S, Henke J, Makalowski W, Jorde L B, Deininger P L, Batzer M A
Departments of Pathology, Genetics Biochemistry and Molecular Biology Stanley S. Scott Cancer Center Neuroscience Center of Excellence, Louisiana State University Health Sciences Center, 1901 Perdido Street, New Orleans 70112, USA.
J Mol Biol. 2001 Aug 3;311(1):17-40. doi: 10.1006/jmbi.2001.4847.
We have utilized computational biology to screen GenBank for the presence of recently integrated Ya5 and Yb8 Alu family members. Our analysis identified 2640 Ya5 Alu family members and 1852 Yb8 Alu family members from the draft sequence of the human genome. We selected a set of 475 of these elements for detailed analyses. Analysis of the DNA sequences from the individual Alu elements revealed a low level of random mutations within both subfamilies consistent with the recent origin of these elements within the human genome. Polymerase chain reaction assays were used to determine the phylogenetic distribution and human genomic variation associated with each Alu repeat. Over 99 % of the Ya5 and Yb8 Alu family members were restricted to the human genome and absent from orthologous positions within the genomes of several non-human primates, confirming the recent origin of these Alu subfamilies in the human genome. Approximately 1 % of the analyzed Ya5 and Yb8 Alu family members had integrated into previously undefined repeated regions of the human genome. Analysis of mosaic Yb8 elements suggests gene conversion played an important role in generating sequence diversity among these elements. Of the 475 evaluated elements, a total of 106 of the Ya5 and Yb8 Alu family members were polymorphic for insertion presence/absence within the genomes of a diverse array of human populations. The newly identified Alu insertion polymorphisms will be useful tools for the study of human genomic diversity.
我们利用计算生物学在GenBank中筛选最近整合的Ya5和Yb8 Alu家族成员。我们的分析从人类基因组草图序列中鉴定出2640个Ya5 Alu家族成员和1852个Yb8 Alu家族成员。我们选择了其中475个元件进行详细分析。对单个Alu元件的DNA序列分析显示,两个亚家族内的随机突变水平较低,这与这些元件在人类基因组中的近期起源一致。聚合酶链反应分析用于确定与每个Alu重复相关的系统发育分布和人类基因组变异。超过99%的Ya5和Yb8 Alu家族成员局限于人类基因组,在几种非人类灵长类动物基因组的直系同源位置中不存在,这证实了这些Alu亚家族在人类基因组中的近期起源。大约1%的分析过的Ya5和Yb8 Alu家族成员已整合到人类基因组中以前未定义的重复区域。对镶嵌Yb8元件的分析表明,基因转换在这些元件之间产生序列多样性方面发挥了重要作用。在475个评估元件中,总共106个Ya5和Yb8 Alu家族成员在多种人类群体的基因组中插入存在/缺失方面具有多态性。新鉴定的Alu插入多态性将成为研究人类基因组多样性的有用工具。