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酿酒酵母TAN1(tRNA乙酰转移酶)在真核起始因子2B(eIF2B)介导的翻译控制和应激反应中的作用。

Role of Saccharomyces cerevisiae TAN1 (tRNA acetyltransferase) in eukaryotic initiation factor 2B (eIF2B)-mediated translation control and stress response.

作者信息

Sharma Sonum, Sourirajan Anuradha, Dev Kamal

机构信息

Faculty of Applied Sciences and Biotechnology, Shoolini University, Solan, Himachal Pradesh, India.

出版信息

3 Biotech. 2017 Jul;7(3):223. doi: 10.1007/s13205-017-0857-8. Epub 2017 Jul 4.

DOI:10.1007/s13205-017-0857-8
PMID:28677085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5496938/
Abstract

Eukaryotic initiation factor 2B (eIF2B) controls the first step of translation by catalyzing guanine nucleotide exchange on eukaryotic initiation factor 2 (eIF2). Mutations in the genes encoding eIF2B subunits inhibit the nucleotide exchange and eventually slow down the process of translation, causing vanishing white matter disease. We constructed a Saccharomyces cerevisiae genomic DNA library in YEp24 vector and screened it for the identification of extragenic suppressors of eIF2B mutations, corresponding to human eIF2B mutations. We found a suppressor-II (Sup-II) genomic clone, as suppressor of eIF2Bβ (gcd7-201) mutation. Identification of Sup-II reveals the presence of truncated SEC15, full-length TAN1 (tRNA acetyltransferase), full-length EMC4, full-length YGL230C (putative protein) and truncated SAP4 genes. Full-length TAN1 (tRNA acetyltransferase) gene, subcloned into pEG(KG) vector and overexpressed in gcd7-201 gcn2∆ strain, suppresses the slow-growth (Slg and general control derepression (Gcd) phenotype of gcd7-201 gcn2∆ mutation, but YGL230C did not show any effect. A GST-Tan1p fusion protein of 60 kDa was detected by western blotting using α-GST antibodies. Interestingly, Tan1p overexpression also suppresses the temperature-sensitive (Ts), Slg and Gcd phenotype of eIF2Bγ (gcd1-502) mutant. Role of Tan1p protein in eIF2B-mediated translation regulation was also studied. Results revealed that Tan1p overexpression confers resistance to GCD7 GCN2, gcd7-201 gcn2∆, GCD7 gcn2∆ growth defect under ethanol, HO and caffeine stress. No resistance to DMSO-, NaCl- and DTT-mediated growth defect upon GCD7 gcn2∆, GCD7 GCN2, gcd7-201 gcn2∆ was observed by overexpression of TAN1. Hence, we proposed that Tan1p is involved directly or indirectly in regulating eIF2B-mediated translation.

摘要

真核生物起始因子2B(eIF2B)通过催化真核生物起始因子2(eIF2)上的鸟嘌呤核苷酸交换来控制翻译的第一步。编码eIF2B亚基的基因突变会抑制核苷酸交换,最终减缓翻译过程,导致脑白质消失症。我们构建了一个以YEp24载体为基础的酿酒酵母基因组DNA文库,并对其进行筛选,以鉴定与人类eIF2B突变相对应的eIF2B突变的基因外抑制子。我们发现了一个抑制子-II(Sup-II)基因组克隆,作为eIF2Bβ(gcd7-201)突变的抑制子。对Sup-II的鉴定揭示了截短的SEC15、全长的TAN1(tRNA乙酰转移酶)、全长的EMC4、全长的YGL230C(假定蛋白)和截短的SAP4基因的存在。将全长的TAN1(tRNA乙酰转移酶)基因亚克隆到pEG(KG)载体中,并在gcd7-201 gcn2Δ菌株中过表达,可抑制gcd7-201 gcn2Δ突变的生长缓慢(Slg)和一般控制去阻遏(Gcd)表型,但YGL230C没有显示任何作用。使用α-GST抗体通过蛋白质印迹法检测到一个60 kDa的GST-Tan1p融合蛋白。有趣的是,Tan1p的过表达也抑制了eIF2Bγ(gcd1-502)突变体的温度敏感(Ts)、Slg和Gcd表型。还研究了Tan1p蛋白在eIF2B介导的翻译调控中的作用。结果表明,Tan1p的过表达赋予了对GCD7 GCN2、gcd7-201 gcn2Δ、GCD7 gcn2Δ在乙醇、HO和咖啡因胁迫下生长缺陷的抗性。通过TAN1的过表达未观察到对GCD7 gcn2Δ、GCD7 GCN2、gcd7-201 gcn2Δ在DMSO、NaCl和DTT介导的生长缺陷的抗性。因此,我们提出Tan1p直接或间接参与调节eIF2B介导的翻译。

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引用本文的文献

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Saccharomyces cerevisiae ER membrane protein complex subunit 4 (EMC4) plays a crucial role in eIF2B-mediated translation regulation and survival under stress conditions.酿酒酵母内质网(ER)膜蛋白复合物亚基4(EMC4)在应激条件下eIF2B介导的翻译调控和细胞存活中起着关键作用。
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本文引用的文献

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Prioritized Expression of BTN2 of Saccharomyces cerevisiae under Pronounced Translation Repression Induced by Severe Ethanol Stress.在严重乙醇胁迫诱导的明显翻译抑制下酿酒酵母BTN2的优先表达
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