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墨西哥利什曼原虫副鞭毛杆蛋白PFR-2的阶段特异性表达。

Stage-specific expression of the Leishmania mexicana paraflagellar rod protein PFR-2.

作者信息

Moore L L, Santrich C, LeBowitz J H

机构信息

Department of Biochemistry, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Mol Biochem Parasitol. 1996 Oct 1;80(2):125-35. doi: 10.1016/0166-6851(96)02688-6.

Abstract

A screen for Leishmania mexicana genes encoding promastigote-specific flagellar proteins resulted in isolation of genes encoding the major components of the paraflagellar rod. One of these, PFR-2, was characterized extensively. PFR-2 genes are present in the genome as a tandem array of three genes designated PFR-2A, PFR-2B, PFR-2C. PFR-2A and PFR-2B are encoded by a 3.1 transcript while PFR-2C is encoded by a 3.8-kb transcript that has a 3' UTR different from that of the 3.1-kb transcript. Both of these mRNAs were 15-fold more abundant in promastigotes than in amastigotes. Two transcripts immediately upstream of the locus were constitutively expressed while two downstream transcripts were fourfold more abundant in promastigotes than in amastigotes. The PFR genes will provide a good model system for analysis of stage-specific gene regulation in Leishmania as well as assist in the characterization of the function and organization of the paraflagellar rod.

摘要

对编码前鞭毛体特异性鞭毛蛋白的墨西哥利什曼原虫基因进行筛选,结果分离出了编码副鞭毛杆主要成分的基因。其中一个基因PFR - 2得到了广泛的表征。PFR - 2基因在基因组中以三个串联排列的基因形式存在,分别命名为PFR - 2A、PFR - 2B和PFR - 2C。PFR - 2A和PFR - 2B由一个3.1kb的转录本编码,而PFR - 2C由一个3.8kb的转录本编码,该转录本的3'UTR与3.1kb转录本的不同。这两种mRNA在前鞭毛体中的丰度均比无鞭毛体高15倍。该基因座上游紧邻的两个转录本组成性表达,而下游的两个转录本在前鞭毛体中的丰度比无鞭毛体高4倍。PFR基因将为分析利什曼原虫阶段特异性基因调控提供一个良好的模型系统,同时有助于对副鞭毛杆的功能和结构进行表征。

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