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酵母中介体中间结构域内的功能和物理相互作用。

Functional and physical interactions within the middle domain of the yeast mediator.

作者信息

Hallberg Magnus, Hu Guo-Zhen, Tronnersjö Susanna, Adler David, Balciunas Darius, Björklund Stefan, Ronne Hans

机构信息

Department of Medical Biochemistry and Biophysics, Umeå University, 0187, Umeå, Sweden.

出版信息

Mol Genet Genomics. 2006 Aug;276(2):197-210. doi: 10.1007/s00438-006-0135-7. Epub 2006 Jun 7.

Abstract

Med21 (Srb7) is a small essential subunit of the middle domain of the Mediator, which is conserved in all eukaryotes. It is thought to play an important role in both transcriptional activation and repression. In the yeast Saccharomyces cerevisiae, Med21 is known to interact both with the Mediator subunit Med6 and the global co-repressor Tup1. We have made a temperature-sensitive med21-ts mutant, which we used in a high copy number suppressor screen. We found ten yeast genes that can suppress the med21-ts mutation in high copy number. The three strongest suppressors were MED7 and MED10 (NUT2), which encode other Mediator subunits, and ASH1, which encodes a repressor of the HO gene. 2-Hybrid experiments confirmed multiple interactions between Med21, Med10, Med7 and Med4, and also revealed a Med21 self-interaction. The interactions of Med21 with Med7 and Med10 were verified by co-immunoprecipitation of tagged proteins produced in insect cells and E. coli, where both interactions were found to depend strongly on the amino acid residues 2-8 of Med21. These interactions, and the interactions of Med21 with Med6 and Tup1, suggest that Med21 may serve as a molecular switchboard that integrates different signals before they reach the core polymerase.

摘要

Med21(Srb7)是中介体中间结构域的一个小的必需亚基,在所有真核生物中都保守。它被认为在转录激活和抑制中都发挥重要作用。在酿酒酵母中,已知Med21与中介体亚基Med6和全局共抑制因子Tup1相互作用。我们构建了一个温度敏感型med21-ts突变体,并将其用于高拷贝数抑制子筛选。我们发现了十个能够在高拷贝数下抑制med21-ts突变的酵母基因。三个最强的抑制子是MED7和MED10(NUT2),它们编码其他中介体亚基,以及ASH1,它编码HO基因的一个抑制子。双杂交实验证实了Med21、Med10、Med7和Med4之间的多种相互作用,还揭示了Med21的自我相互作用。通过对昆虫细胞和大肠杆菌中产生的标签蛋白进行共免疫沉淀,验证了Med21与Med7和Med10的相互作用,发现这两种相互作用都强烈依赖于Med21的第2至8个氨基酸残基。这些相互作用,以及Med21与Med6和Tup1的相互作用,表明Med21可能作为一个分子转接板,在不同信号到达核心聚合酶之前对它们进行整合。

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