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一种磷酸甘油酸变位酶脑同工型(PGAM 1)假基因定位于人类门克斯病基因(ATP7 A)内。

A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7 A).

作者信息

Dierick H A, Mercer J F, Glover T W

机构信息

Department of Pediatrics, University of Michigan, Ann Arbor 48109-0618, USA.

出版信息

Gene. 1997 Oct 1;198(1-2):37-41. doi: 10.1016/s0378-1119(97)00289-8.

Abstract

We have identified a phosphoglycerate mutase brain isoform (PGAM 1, PGAM B) cDNA that is localized between exons 1 and 2 of the Menkes disease gene (ATP7 A, MNK) at Xq13.3. The cDNA shows 98% identity to the previously identified PGAM 1 cDNA (Sakoda et al., J. Biol. Chem. 263 (1988) 16899-16905) and probably represents a recent retroposition of this parent PGAM 1 mRNA. Although the typical features of a processed pseudogene are present, the open reading frame (ORF) of this PGAM cDNA is potentially expressed. There are 11 bp changes in the 765 bp ORF, none of which are nonsense mutations or deletions. The region upstream from the ORF shows some features of a possible promoter region, although it lacks a CpG island often associated with functional promoters. We analyzed the expression of this PGAM 1 cDNA using RT-PCR followed by restriction enzyme digestion based on a 1 bp missmatch in this cDNA to distinguish it from normal PGAM 1 gene expression. With this sensitive method, we could not find expression in any of the tissues examined. Taken together, we conclude that the PGAM 1 cDNA upstream from exon 2 of the Menkes gene is likely to be a processed pseudogene originating from a very recent retroposition of a PGAM 1 transcript. To our knowledge this is the first report of a pseudogene located within a gene.

摘要

我们鉴定出一种磷酸甘油酸变位酶脑同工型(PGAM 1,PGAM B)的cDNA,其定位于Xq13.3处的门克斯病基因(ATP7 A,MNK)第1外显子和第2外显子之间。该cDNA与先前鉴定的PGAM 1 cDNA显示出98%的同一性(坂田等人,《生物化学杂志》263卷(1988年)16899 - 16905页),可能代表了该亲本PGAM 1 mRNA近期的反转录转座。尽管存在加工假基因的典型特征,但该PGAM cDNA的开放阅读框(ORF)有潜在表达能力。在765 bp的ORF中有11个碱基变化,其中没有一个是无义突变或缺失。ORF上游区域显示出一些可能的启动子区域特征,尽管它缺乏通常与功能性启动子相关的CpG岛。我们使用逆转录聚合酶链反应(RT-PCR),然后基于该cDNA中的1个碱基错配进行限制性内切酶消化来分析此PGAM 1 cDNA的表达,以将其与正常PGAM 1基因表达区分开来。通过这种灵敏的方法,我们在任何检测的组织中都未发现表达。综上所述,我们得出结论,门克斯基因第2外显子上游的PGAM 1 cDNA可能是一个加工假基因,源自PGAM 1转录本近期的反转录转座。据我们所知,这是关于位于一个基因内的假基因的首次报道。

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