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PPB1,一种克氏锥虫中假定的剪接前导RNA基因转录因子。

PPB1, a putative spliced leader RNA gene transcription factor in Trypanosoma cruzi.

作者信息

Wen L M, Xu P, Benegal G, Carvalho M R, Buck G A

机构信息

Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond 23298-0678, USA.

出版信息

Mol Biochem Parasitol. 2000 Oct;110(2):207-21. doi: 10.1016/s0166-6851(00)00271-1.

Abstract

In trypanosomatids, the spliced leader RNA, or SL RNA, donates its 5' 39 nucleotides to mature nuclear mRNAs in a process termed trans-splicing. We have previously characterized the SL RNA gene from Trypanosoma cruzi and identified its transcription promoter, including a 14 nt proximal sequence element, or PSE, that binds a putative transcription factor and activates transcription of the gene. Herein, we describe establishment of a yeast one-hybrid system using the 14 nt PSE as bait, and use this system to select T. cruzi cDNAs encoding a putative transcription factor that activates transcription of the SL RNA gene. The cDNA was selected from a normalized library and encodes an approximately 45 kDa putative PSE promoter-binding protein, PPB1. PPB1 in vitro translated or overexpressed in and isolated from transformed E. coli, showed PSE-specific binding activity by electrophoretic mobility shift assays. Finally, overexpression of PPB1 in T. cruzi led to increased expression of the SL RNA gene as well as reporter genes in episomal constructs under the control of the SL RNA gene promoter. These observations suggest that PPB1 is a transcription factor that plays an important role in SL RNA gene expression.

摘要

在锥虫中,剪接前导RNA(SL RNA)通过一种称为反式剪接的过程,将其5'端的39个核苷酸提供给成熟的核mRNA。我们之前已对克氏锥虫的SL RNA基因进行了表征,并鉴定了其转录启动子,其中包括一个14 nt的近端序列元件(PSE),该元件可结合一种假定的转录因子并激活该基因的转录。在此,我们描述了一种以14 nt的PSE为诱饵的酵母单杂交系统的建立,并利用该系统筛选编码可激活SL RNA基因转录的假定转录因子的克氏锥虫cDNA。该cDNA是从一个标准化文库中筛选出来的,编码一种约45 kDa的假定PSE启动子结合蛋白PPB1。体外翻译或在转化大肠杆菌中过表达并分离得到的PPB1,通过电泳迁移率变动分析显示出PSE特异性结合活性。最后,在克氏锥虫中过表达PPB1导致在SL RNA基因启动子控制下的附加型构建体中SL RNA基因以及报告基因的表达增加。这些观察结果表明,PPB1是一种在SL RNA基因表达中起重要作用的转录因子。

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