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转位的人类免疫球蛋白Vκ基因区域携带保守序列元件簇。

Transposed human immunoglobulin V kappa gene regions carry clusters of conserved sequence elements.

作者信息

Lötscher E, Siwka W, Zimmer F J, Grummt F, Zachau H G

机构信息

Institut für Physiologische Chemie, Universität München, F.R.G.

出版信息

Gene. 1988 Sep 30;69(2):225-36. doi: 10.1016/0378-1119(88)90433-7.

Abstract

The V kappa I gene regions which have been transposed in evolution from the site of the kappa locus on chromosome 2 to chromosomes 1, 22, and other chromosomes, are very similar and may have been derived from one ancestor gene. Upstream from the transposed genes (called orphons) two types of conserved sequence elements were found using a mouse cell assay system. One type is homologous to the murine sequences which were previously thought to be ARS elements; the other one is related to the binding site of the replication/transcription factor NFIII. Such a combination of elements was seen neither in hybridization experiments with the 1 Mb of the kappa locus available on cosmid clones nor in a computer-aided search of sequence data libraries. We speculate that in the evolutionary past, the clustered elements played a role in the transposition of the V kappa genes, perhaps by causing an over-replication and/or by facilitating the integration of the genes.

摘要

VκI基因区域在进化过程中已从2号染色体上的κ基因座位点转座到1号、22号和其他染色体上,它们非常相似,可能源自一个祖先基因。利用小鼠细胞检测系统,在转座基因(称为孤基因)的上游发现了两种类型的保守序列元件。一种类型与先前被认为是自主复制序列元件的小鼠序列同源;另一种与复制/转录因子NFIII的结合位点相关。在与黏粒克隆上可用的1 Mb κ基因座进行的杂交实验中,以及在对序列数据库的计算机辅助搜索中,均未发现这种元件组合。我们推测,在进化过程中,这些成簇的元件可能在Vκ基因的转座中发挥了作用,也许是通过导致过度复制和/或促进基因整合来实现的。

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