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应激反应元件(STRE)和Msn2p调控下的基因在耐乙醇清酒酵母“协会11号”中的表达上调

Elevated expression of genes under the control of stress response element (STRE) and Msn2p in an ethanol-tolerance sake yeast Kyokai no. 11.

作者信息

Watanabe Mamoru, Tamura Kenichi, Magbanua Jose Paolo, Takano Kaname, Kitamoto Katsuhiko, Kitagaki Hiroshi, Akao Takeshi, Shimoi Hitoshi

机构信息

Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashihiroshima 739-8530, Japan.

出版信息

J Biosci Bioeng. 2007 Sep;104(3):163-70. doi: 10.1263/jbb.104.163.

Abstract

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.

摘要

清酒酵母菌株京之华11号(K11)是京之华7号(K7)菌株的乙醇耐受突变体,在乙醇溶液中的存活率高于K7菌株。为阐明该菌株乙醇耐受性的潜在机制,使用DNA微阵列分析了K7和K11的基因表达谱。结果表明,许多受应激诱导的基因在未受应激的K11菌株中高度表达。对K11菌株中与K7菌株相比表达量最高的基因之一HSP12进行分析,发现K11菌株的一个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受一种称为应激反应元件(STRE)的顺式作用因子调控。将STRE序列添加到报告基因的启动子区域导致K11菌株中组成型高水平表达。据报道,转录因子Msn2p和Msn4p与STRE序列结合。对K7和K11菌株的MSN2和MSN4进行DNA序列分析,发现只有Msn2p在这些菌株中具有功能。当K11菌株中的两个Msn2p拷贝被破坏时,受STRE调控的报告基因的表达水平降至K7菌株的水平,表明Msn2p是K11中STRE调控基因高表达所必需的。

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