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人类CALM1钙调蛋白基因的结构以及两个与CALM1相关的假基因CALM1P1和CALM1P2的鉴定。

Structure of the human CALM1 calmodulin gene and identification of two CALM1-related pseudogenes CALM1P1 and CALM1P2.

作者信息

Rhyner J A, Ottiger M, Wicki R, Greenwood T M, Strehler E E

机构信息

Laboratory for Biochemistry, Swiss Federal Institute of Technology, ETH Zentrum, Zurich.

出版信息

Eur J Biochem. 1994 Oct 1;225(1):71-82. doi: 10.1111/j.1432-1033.1994.00071.x.

Abstract

The human CALM1 calmodulin gene has been isolated and characterized. The gene contains six exons spread over about 10 kb of genomic DNA. The exon-intron structure is identical to that of the human CALM3 and of the rat CALM1 and CALM3 genes. A cluster of transcription-start sites was identified 200 bp upstream of the ATG translation-start codon, and several putative regulatory elements were found in the 5' flanking region as well as in intron 1. Sequence comparison with the rat CALM1 gene revealed significant similarities in the promoter regions of the two genes and an even more striking degree of identity (70%) in the available intron 1 sequences. A short CAG trinucleotide repeat region was identified in the 5' untranslated region of the human CALM1 gene; this sequence is not conserved in the rat counterpart. Expression of the CALM1 gene was detected in all human tissues tested, although at varying levels. A 1.7-kb mRNA was uniformly present at comparable levels, whereas a 4.2-kb mRNA species was particularly abundant in brain and skeletal muscle. Clones for two different CALM1-related pseudogenes CALM1P1 and CALM1P2 were also isolated and characterized. Both pseudogenes are intronless and non-functional as judged from the presence of mutations abolishing the open reading frame. Genomic Southern analysis indicates that the human CALM1 gene/pseudogene subfamily comprises at least three but probably no more than four members. The entire family consists of three bona fide CALM genes, at least one expressed calmodulin-like CALML gene as well as at least five pseudogenes.

摘要

人类CALM1钙调蛋白基因已被分离并进行了特征分析。该基因包含六个外显子,分布在约10 kb的基因组DNA上。外显子-内含子结构与人类CALM3以及大鼠CALM1和CALM3基因相同。在ATG翻译起始密码子上游200 bp处鉴定出一组转录起始位点,并且在5'侧翼区域以及内含子1中发现了几个推定的调控元件。与大鼠CALM1基因的序列比较显示,这两个基因的启动子区域存在显著相似性,并且在可用的内含子1序列中具有更高的同一性(70%)。在人类CALM1基因的5'非翻译区鉴定出一个短的CAG三核苷酸重复区域;该序列在大鼠对应物中不保守。在所有测试的人类组织中均检测到CALM1基因的表达,尽管表达水平各不相同。1.7 kb的mRNA以相当的水平均匀存在,而4.2 kb的mRNA种类在脑和骨骼肌中特别丰富。还分离并鉴定了两个不同的与CALM1相关的假基因CALM1P1和CALM1P2的克隆。从消除开放阅读框的突变存在情况判断,这两个假基因均无内含子且无功能。基因组Southern分析表明,人类CALM1基因/假基因亚家族至少包含三个成员,但可能不超过四个。整个家族由三个真正的CALM基因、至少一个表达的钙调蛋白样CALML基因以及至少五个假基因组成。

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