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首页> 外文期刊>Nucleic Acids Research >Trypanosome spliced leader RNA genes contain the first identified RNApolymerase II gene promoter in these organisms
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Trypanosome spliced leader RNA genes contain the first identified RNApolymerase II gene promoter in these organisms

机译:锥虫剪接的前导RNA基因在这些生物体中包含第一个鉴定出的RNApolymerase II基因启动子

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摘要

Typical general transcription factors, such as TATA binding protein and TFII B, have not yet been identified in any member of the Trypanosomatidae family of parasitic protozoa, Interestingly, mRNA coding genes do not appear to have discrete transcriptional start sites, although in most cases they require an RNA polymerase that has the biochemical properties of eukaryotic RNA polymerase II. A discrete transcription initiation site may not be necessary for mRNA synthesis since the sequences upstream of each transcribed coding region are trimmed from the nascent transcript when a short m(7)G-capped RNA is added during mRNA maturation. This short 39 nt m7G-capped RNA, the spliced leader (SL) sequence, is expressed as an similar to 100 nt long RNA from a set of reiterated, though independently transcribed, genes in the trypanosome genome. Punctuation of the 5' end of mRNAs by a m(7)G cap-containing spliced leader is a developing theme in the lower eukaryotic world; organisms as diverse as Euglena and nematode worms, including Caenorhabditis elegans, utilize SL RNA in their mRNA maturation programs. Towards understanding the coordination of SL RNA and mRNA expression in trypanosomes, we have begun by characterizing SL RNA gene expression in the model trypanosome Leptomonas seymouri, Using a homologous in vitro transcription system, we demonstrate in this study that the SL RNA is transcribed by RNA polymerase II, During SL RNA transcription, accurate initiation is determined by an initiator element with a loose consensus of CYAC/AYR(+1). This element, as well as two additional basal promoter elements, is divergent in sequence from the basal transcription elements seen in other eukaryotic gene promoters. We show here that the in vitro transcription extract contains a binding activity that is specific for the initiator element and thus may participate in recruiting RNA polymerase II to the SL RNA gene promoter.
机译:尚未在寄生虫原生动物锥虫科的任何成员中鉴定出典型的一般转录因子,例如TATA结合蛋白和TFIIB。有趣的是,mRNA编码基因似乎没有离散的转录起始位点,尽管在大多数情况下它们需要具有真核RNA聚合酶II的生化特性的RNA聚合酶。对于mRNA合成而言,离散的转录起始位点可能不是必需的,因为在mRNA成熟过程中添加短的m(7)G帽RNA时,每个转录的编码区上游的序列都会从新生的转录物中修剪掉。这种短的39 nt m7G​​封闭的RNA(剪接的前导(SL)序列)表达为类似于锥虫体基因组中一组经过反复重申但独立转录的基因的100 nt长RNA。在较低的真核生物世界中,一个带有m(7)G帽的剪接的前导体标出mRNA的5'端是一个发展中的主题。包括夜蛾和线虫在内的各种生物,包括秀丽隐杆线虫,都在其mRNA成熟程序中利用SL RNA。为了理解锥虫中SL RNA和mRNA表达的协调,我们已经开始通过表征锥虫Leptomonas seymouri模型中SL RNA基因的表达来开始研究。我们使用同源的体外转录系统证明了SL RNA是通过RNA转录的聚合酶II,在SL RNA转录过程中,准确的启动是由与CYAC / AYR(+1)一致的启动子元件决定的。该元件以及两个其他基础启动子元件在序列上与其他真核基因启动子中的基础转录元件在序列上有所不同。我们在这里显示体外转录提取物包含特定于引发剂元件的结合活性,因此可能参与将RNA聚合酶II募集到SL RNA基因启动子。

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