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酿酒酵母RNA聚合酶III的C31亚基中的突变影响转录起始。

A mutation in the C31 subunit of Saccharomyces cerevisiae RNA polymerase III affects transcription initiation.

作者信息

Thuillier V, Stettler S, Sentenac A, Thuriaux P, Werner M

机构信息

Service de Biochimie et Génétique Moléculaire, Gif-sur-Yvette, France.

出版信息

EMBO J. 1995 Jan 16;14(2):351-9. doi: 10.1002/j.1460-2075.1995.tb07009.x.

DOI:10.1002/j.1460-2075.1995.tb07009.x
PMID:7835345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC398089/
Abstract

The C31 subunit belongs to a complex of three subunits (C31, C34 and C82) specific to RNA polymerase (pol) III that have no counterparts in other RNA polymerases. This complex is thought to play a role in transcription initiation since it interacts with the general initiation factor TFIIIB via subunit C34. We have obtained a conditional mutation of pol III by partially deleting the acidic C-terminus of the C31 subunit. A Saccharomyces cerevisiae strain carrying this truncated C31 subunit is impaired in in vivo transcription of tRNAs and failed to grow at 37 degrees C. This conditional growth phenotype was suppressed by overexpression of the gene coding for the largest subunit of pol III (C160), suggesting an interaction between C160 and C31. The mutant pol III enzyme transcribed non-specific templates at wild-type rates in vitro, but was impaired in its capacity to transcribe tRNA genes in the presence of general initiation factors. Transcription initiation, but not termination or recycling of the enzyme, was affected in the mutant, suggesting that it could be altered on interaction with initiation factors or on the formation of the open complex. Interestingly, the C-terminal deletion was also suppressed by a high gene dosage of the DED1 gene encoding a putative helicase.

摘要

C31亚基属于RNA聚合酶(pol)III特有的由三个亚基(C31、C34和C82)组成的复合体,其他RNA聚合酶中没有与之对应的亚基。由于该复合体通过C34亚基与通用起始因子TFIIIB相互作用,因此被认为在转录起始中发挥作用。我们通过部分缺失C31亚基的酸性C末端获得了pol III的条件性突变。携带这种截短C31亚基的酿酒酵母菌株在tRNA的体内转录中受损,并且在37℃下无法生长。这种条件性生长表型被pol III最大亚基(C160)编码基因的过表达所抑制,这表明C160和C31之间存在相互作用。突变的pol III酶在体外以野生型速率转录非特异性模板,但在存在通用起始因子的情况下转录tRNA基因的能力受损。该突变体中酶的转录起始受到影响,但终止或循环不受影响,这表明它在与起始因子相互作用或形成开放复合体时可能发生了改变。有趣的是,编码假定解旋酶的DED1基因的高基因剂量也抑制了C末端缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/47061a8773d5/emboj00026-0158-c.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/2e89eefc3092/emboj00026-0158-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/47061a8773d5/emboj00026-0158-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/fb7f4638e20e/emboj00026-0154-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/54be03a7ade9/emboj00026-0155-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/bd941a5f7910/emboj00026-0157-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/430de2e00432/emboj00026-0157-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e1e/398089/2e89eefc3092/emboj00026-0158-a.jpg
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