Suppr超能文献

墨西哥利什曼原虫CPB半胱氨酸蛋白酶的阶段调控表达由基因间序列元件介导。

The stage-regulated expression of Leishmania mexicana CPB cysteine proteases is mediated by an intercistronic sequence element.

作者信息

Brooks D R, Denise H, Westrop G D, Coombs G H, Mottram J C

机构信息

Wellcome Centre for Molecular Parasitology, University of Glasgow, the Anderson College, 56 Dumbarton Road, Glasgow G11 6NU, Scotland, United Kingdom.

出版信息

J Biol Chem. 2001 Dec 14;276(50):47061-9. doi: 10.1074/jbc.M108498200. Epub 2001 Oct 9.

Abstract

The tandemly arranged CPB genes of Leishmania mexicana are polycistronically transcribed and encode cysteine proteases that are differentially stage-specific; CPB1 and CPB2 are expressed predominantly in metacyclics, whereas CPB3-CPB18 are expressed mainly in amastigotes. The mechanisms responsible for this differential expression have been studied via gene analysis and re-integration of individual CPB genes, and variants thereof, into a CPB-deficient parasite mutant. Comparison of the nucleotide sequences of the repeat units of CPB1 and CPB2 with CPB2.8 (typical of CPB3-CPB18) revealed two major regions of divergence as follows: one of 258 base pairs (bp) corresponding to the C-terminal extension of CPB2.8; another, designated InS, of 120 bp, with insertions totaling 57 bp, localized to the intercistronic region downstream of CPB1 and CPB2. Cell lines expressing CPB2.8 or CPB2 with the 3'-untranslated region and intercistronic sequence of CPB2.8 showed up-regulation in amastigotes. Conversely, metacyclic-specific expression occurred with CPB2 or CPB2.8 with the 3'-untranslated region and intercistronic sequence of CPB2. Moreover, the InS down-regulated expression in amastigotes of a reporter gene integrated into the CPB locus. It is proposed that the InS mediates metacyclic-specific stage-regulated expression of CPB by affecting the maturation of polycistronic pre-mRNA. This is the first well defined cis-regulatory element implicated in post-transcriptional stage-specific gene expression in Leishmania.

摘要

墨西哥利什曼原虫串联排列的CPB基因进行多顺反子转录,编码具有不同阶段特异性的半胱氨酸蛋白酶;CPB1和CPB2主要在循环后期表达,而CPB3 - CPB18主要在无鞭毛体中表达。通过基因分析以及将单个CPB基因及其变体重新整合到CPB缺陷型寄生虫突变体中,研究了导致这种差异表达的机制。将CPB1和CPB2的重复单元核苷酸序列与CPB2.8(CPB3 - CPB18的典型代表)进行比较,发现两个主要的差异区域如下:一个是258个碱基对(bp),对应于CPB2.8的C末端延伸;另一个是120 bp的区域,称为InS,有总共57 bp的插入,位于CPB1和CPB2下游的顺反子间区域。表达带有CPB2.8的3' - 非翻译区和顺反子间序列的CPB2.8或CPB2的细胞系在无鞭毛体中出现上调表达。相反,带有CPB2的3' - 非翻译区和顺反子间序列的CPB2或CPB2.8出现循环后期特异性表达。此外,InS下调了整合到CPB基因座的报告基因在无鞭毛体中的表达。有人提出,InS通过影响多顺反子前体mRNA的成熟来介导CPB的循环后期特异性阶段调控表达。这是第一个明确涉及利什曼原虫转录后阶段特异性基因表达的顺式调控元件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验