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首页> 外文期刊>Journal of Bioscience and Bioengineering >Elevated Expression of Genes under the Control of Stress Response Element(STRE)and Msn2p in an Ethanol-Tolerance Sake Yeast Kyokai No.11
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Elevated Expression of Genes under the Control of Stress Response Element(STRE)and Msn2p in an Ethanol-Tolerance Sake Yeast Kyokai No.11

机译:耐酒精性清酒协和11号受应激反应元件(STRE)和Msn2p控制的基因表达升高

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摘要

The sake yeast strain Kyokai no.11(K11)is an ethanol-tolerant mutant of strain Kyokai no.7(K7),which shows higher viability in an ethanol solution than strain K7.To clarify the mechanism underlying the ethanol tolerance of this strain,the gene expression profiles of K7 and K11 were analyzed using DNA microarrays.The results indicate that many genes induced by stresses were highly expressed in strain K11 not exposed to stresses.Analysis of HSP12,one of the most highly expressed genes in strain K11 compared with strain K7,revealed that a trans-acting factor of strain K11 was involved in the elevated expression of HSP12.Many of the highly expressed genes in strain K11 including HSP12 were under the control of a cis-acting factor called the stress response element(STRE).The addition of STRE sequences to a promoter region of a reporter gene resulted in constitutive high-level expression in strain K11.It was reported that transcription factors Msn2p and Msn4p bind to STRE sequences.DNA sequence analyses of MSN2 and MSN4 of strains K7 and K11 revealed that only Msn2p was functional in these strains.When two copies of MSN2 in strain K11 were disrupted,the expression level of the reporter gene under the control of STRE decreased to the level of strain K7,indicating that Msn2p is required for the elevated expression of the STRE-controlled genes in K11.
机译:日本清酒酵母菌株Kkaikai No.11(K11)是Kyokai No.7(K7)菌株的耐乙醇突变体,在乙醇溶液中比K7菌株具有更高的生存力。用DNA芯片分析了K7和K11的基因表达谱。结果表明,应激诱导的许多基因在未暴露于胁迫的菌株K11中高表达。HSP12分析是菌株K11中表达最强的基因之一揭示了K11菌株的反式作用因子参与了HSP12的高表达.K11菌株中包括HSP12在内的许多高表达基因均受称为应力响应元件的顺式作用因子的控制(将STRE序列添加到报告基因的启动子区域导致K11菌株进行组成型高水平表达,据报道转录因子Msn2p和Msn4p结合到STRE序列。通过对菌株K7和K11的MSN2和MSN4的分析发现,在这些菌株中只有Msn2p起作用。当菌株K11中的两个MSN2拷贝被破坏时,在STRE控制下的报告基因的表达水平下降到菌株的水平。 K7,表明Msn2p是K11中STRE调控基因表达升高所必需的。

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