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旧世界猴的成年α-珠蛋白基因座:Alu家族重复序列插入位点界定了与人类序列相似性的突然中断。

The adult alpha-globin locus of Old World monkeys: an abrupt breakdown of sequence similarity to human is defined by an Alu family repeat insertion site.

作者信息

Shaw J P, Marks J, Shen C K

机构信息

Department of Genetics, University of California, Davis 95616.

出版信息

J Mol Evol. 1991 Dec;33(6):506-13. doi: 10.1007/BF02102803.

Abstract

The haploid genomes of all known primates have two or more adult alpha-globin genes contained within tandemly arranged duplication units. Although the tandem duplication event generating these alpha-globin loci is believed to occur prior to the divergence of primates, a number of length polymorphisms exist within the loci among different primate species. In order to understand the molecular basis of these length polymorphisms, we have cloned and determined the nucleotide sequence of a major portion of the rhesus monkey adult alpha-globin locus. Sequence comparison to human suggests that the length difference between the adult alpha-globin loci of human and Old World monkey is the result of one or more DNA recombination processes, all of which appeared to be related to the transposition of Alu family repeats. First, the finding of a monomeric Alu family repeat at the junction between nonhomology block I and homology block Y of the alpha 2 gene-containing unit in rhesus macaque suggests that the dimeric Alu family repeat, Alu 3, at the orthologous position in human was generated by insertion of a monomeric Alu family repeat into the 3' end of another preexisting Alu family repeat. Second, two Alu family repeats, Alu 1 and Alu 2, exist in human at the 3' end of each of the two X homology blocks, respectively. However, this pair of paralogous Alu family repeats is absent at the corresponding positions in rhesus macaques. This raises interesting questions regarding the evolutionary origin of Alu 1 and Alu 2. Finally, DNA sequences immediately downstream from the insertion site of Alu 2 are completely different between human and rhesus macaque.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

所有已知灵长类动物的单倍体基因组都有两个或更多成体α-珠蛋白基因,这些基因包含在串联排列的重复单元中。尽管产生这些α-珠蛋白基因座的串联重复事件被认为发生在灵长类动物分化之前,但不同灵长类物种的基因座内存在许多长度多态性。为了理解这些长度多态性的分子基础,我们克隆并测定了恒河猴成体α-珠蛋白基因座主要部分的核苷酸序列。与人类的序列比较表明,人类和旧世界猴成体α-珠蛋白基因座之间的长度差异是一个或多个DNA重组过程的结果,所有这些过程似乎都与Alu家族重复序列的转座有关。首先,在恒河猴含α2基因单元的非同源块I和同源块Y之间的连接处发现了一个单体Alu家族重复序列,这表明人类直系同源位置的二聚体Alu家族重复序列Alu 3是由一个单体Alu家族重复序列插入另一个预先存在的Alu家族重复序列的3'端产生的。其次,人类在两个X同源块的每一个的3'端分别存在两个Alu家族重复序列Alu 1和Alu 2。然而,恒河猴的相应位置没有这对旁系同源Alu家族重复序列。这就引发了关于Alu 1和Alu 2进化起源的有趣问题。最后,人类和恒河猴之间Alu 2插入位点下游的DNA序列完全不同。(摘要截短于250字)

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