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河豚红鳍东方鲀中小核RNA(snRNA)及snRNA型基因的特征分析。

Characterization of snRNA and snRNA-type genes in the pufferfish Fugu rubripes.

作者信息

Myslinski Evelyne, Krol Alain, Carbon Philippe

机构信息

UPR 9002 du CNRS, Structure des Macromolécules Biologiques et Mécanismes de Reconnaissance, Institut de Biologie Moléculaire et Cellulaire 15, rue René Descartes, 67084 Strasbourg Cedex, France.

出版信息

Gene. 2004 Apr 14;330:149-58. doi: 10.1016/j.gene.2004.01.021.

Abstract

Vertebrate snRNA and snRNA-type genes occur in independent transcription units with external promoters. The transcription level from the basal promoter is enhanced by the distal sequence element DSE. This element contains almost invariably two activator submotifs, the Staf binding site and the octamer motif, recruiting the Staf and Oct-1 transcriptional activators. In the present work, database search identified 35 snRNA and snRNA-type genes in the genome sequence of the pufferfish Fugu rubripes. Sequence comparisons of promoter elements, determination of template activities by microinjection into Xenopus oocytes and DNA binding assays of the transcriptional activators led to the surprising finding that only two Fugu genes conform to the general scheme with the expected two submotifs in the DSE. Distinctively, all the other DSEs harbor a unique Staf binding site. Also striking was the observation that the tRNA(Sec), and the snRNA genes that are tandemly repeated, are transcribed from promoter-less DSEs. Evolutionary implications of these results are discussed.

摘要

脊椎动物的小核RNA(snRNA)和snRNA型基因存在于具有外部启动子的独立转录单元中。基础启动子的转录水平会被远端序列元件(DSE)增强。该元件几乎总是包含两个激活子基序,即Staf结合位点和八聚体基序,它们可招募Staf和Oct-1转录激活因子。在本研究中,通过数据库搜索在河豚红鳍东方鲀的基因组序列中鉴定出35个snRNA和snRNA型基因。对启动子元件进行序列比较、通过显微注射到非洲爪蟾卵母细胞中来测定模板活性以及对转录激活因子进行DNA结合分析,结果发现了一个惊人的现象:在河豚中只有两个基因符合一般模式,即DSE中具有预期的两个基序。特别的是,所有其他DSE都含有一个独特的Staf结合位点。同样引人注目的是,发现串联重复的tRNA(Sec)和snRNA基因是从无启动子的DSE转录而来的。本文还讨论了这些结果的进化意义。

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