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布氏锥虫剪接前导RNA基因的转录仅取决于上游调控元件的存在。

Transcription of the Trypanosoma brucei spliced leader RNA gene is dependent only on the presence of upstream regulatory elements.

作者信息

Günzl A, Ullu E, Dörner M, Fragoso S P, Hoffmann K F, Milner J D, Morita Y, Nguu E K, Vanacova S, Wünsch S, Dare A O, Kwon H, Tschudi C

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520-8022, USA.

出版信息

Mol Biochem Parasitol. 1997 Mar;85(1):67-76. doi: 10.1016/s0166-6851(96)02816-2.

Abstract

The spliced leader (SL) RNA plays a key role in mRNA maturation in trypanosomatid protozoa by providing the SL sequence, which is joined to the 5' end of every mRNA. As a first step towards a better understanding of the biogenesis and function of the SL RNA, we expressed a tagged SL RNA gene in a cell-free system of procyclic Trypanosoma brucei cells. Transcription initiates at + 1 can be detected as early as 1 min after addition of extract. Transcription of the SL RNA gene in vitro, as well as in permeable cells, is mediated by an alpha-amanitin/tagetitoxin resistant complex, suggesting a promoter that is intermediate between a classical RNA polymerase II and RNA polymerase III promoter. An analysis of the promoter architecture of the SL RNA gene revealed that regulatory elements are located upstream of the coding region and that the SL sequence, in contrast to the nematode SL sequence, is not required for T. brucei SL RNA gene transcription.

摘要

剪接前导序列(SL)RNA通过提供与每个mRNA 5'端相连的SL序列,在锥虫原生动物的mRNA成熟过程中发挥关键作用。作为更好地理解SL RNA生物发生和功能的第一步,我们在布氏锥虫前循环细胞的无细胞系统中表达了一个带有标签的SL RNA基因。转录起始于+1,在加入提取物后1分钟即可最早检测到。SL RNA基因在体外以及在可渗透细胞中的转录由一种对α-鹅膏菌素/tagetitoxin抗性的复合物介导,这表明存在一个介于经典RNA聚合酶II和RNA聚合酶III启动子之间的启动子。对SL RNA基因启动子结构的分析表明,调控元件位于编码区上游,并且与线虫的SL序列不同,布氏锥虫SL RNA基因转录不需要SL序列。

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