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粗糙脉孢菌5S rRNA和tRNA基因的所有内部启动子元件,包括A框,在功能上都是基因特异性的。

All internal promoter elements of Neurospora crassa 5 S rRNA and tRNA genes, including the A boxes, are functionally gene-specific.

作者信息

Shi Y G, Tyler B M

机构信息

Department of Plant Pathology, University of California, Davis 95616.

出版信息

J Biol Chem. 1991 May 5;266(13):8015-9.

PMID:1827115
Abstract

The internal control elements of Neurospora crassa 5 S genes include an A box and a C box as in Xenopus and Saccharomyces cerevisiae, plus a novel element, the Ribo box at position +18 to +34. The Ribo box is also found in the 40 S rRNA promoter and a ribosomal protein gene but is absent from tRNA genes in N. crassa. The 5 S A box diverges from the tRNA A box consensus at two positions. We tested whether replacement of the 5 S A box with a tRNALeu A box sequence would increase 5 S gene transcription in vitro or would remove the requirement for the Ribo box. The 5 S gene with the tRNALeu A box was transcribed poorly, and the Ribo box and the C box are still required for transcription. We tested the function of the Ribo box and 5 S A box in a tRNA-like transcription unit by constructing hybrids between a 5 S gene and a tRNALeu gene. In the tRNA-like context, the 5 S A box supported a lower level of transcription than the tRNA A box, and the Ribo box was not required at all. Therefore, in N. crassa, all of the 5 S internal control elements are gene-specific. In particular, the 5 S and tRNA A box sequences are not functionally interchangeable and may bind different transcription factors. Transcription of the hybrids was initiated at the 5 S initiation site, suggesting that the mechanism of initiation site selection is the same in the 5 S and tRNA genes. Competition experiments with the tRNA B box suggested that the N. crassa 5 S and tRNA genes require at least one common transcription factor such as TFIIIC.

摘要

粗糙脉孢菌5S基因的内部控制元件包括与非洲爪蟾和酿酒酵母中类似的A框和C框,另外还有一个新元件,即位于+18至+34位置的核糖体框(Ribo box)。核糖体框也存在于40S rRNA启动子和一个核糖体蛋白基因中,但在粗糙脉孢菌的tRNA基因中不存在。5S A框在两个位置上与tRNA A框共有序列不同。我们测试了用tRNALeu A框序列替换5S A框是否会在体外增加5S基因的转录,或者是否会消除对核糖体框的需求。带有tRNALeu A框的5S基因转录效果很差,转录仍然需要核糖体框和C框。我们通过构建5S基因和tRNALeu基因之间的杂种,测试了核糖体框和5S A框在类似tRNA的转录单元中的功能。在类似tRNA的环境中,5S A框支持的转录水平低于tRNA A框,并且完全不需要核糖体框。因此,在粗糙脉孢菌中,所有5S内部控制元件都是基因特异性的。特别是,5S和tRNA A框序列在功能上不可互换,可能结合不同的转录因子。杂种的转录在5S起始位点开始,这表明5S和tRNA基因中起始位点选择的机制是相同的。与tRNA B框的竞争实验表明,粗糙脉孢菌5S和tRNA基因至少需要一种共同的转录因子,如TFIIIC。

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