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Rpb4的保守区域和非保守区域参与了酿酒酵母中的多种表型。

The conserved and non-conserved regions of Rpb4 are involved in multiple phenotypes in Saccharomyces cerevisiae.

作者信息

Sampath Vinaya, Rekha Nambudiry, Srinivasan N, Sadhale Parag

机构信息

Department of Microbiology & Cell Biology, Indian Institute of Science, Bangalore 560012, India.

出版信息

J Biol Chem. 2003 Dec 19;278(51):51566-76. doi: 10.1074/jbc.M305863200. Epub 2003 Oct 6.

Abstract

Rpb4, the fourth largest subunit of RNA polymerase II in Saccharomyces cerevisiae, is required for many phenotypes, including growth at high and low temperatures, sporulation, pseudohyphal growth, activated transcription of a subset of genes, and efficient carbon and energy metabolism. We have used deletion analysis to delineate the domains of the protein involved in these multiple phenotypes. The scRpb4 protein is conserved at the N and C termini but possesses certain non-conserved regions in the central portion. Our deletion analysis and molecular modeling results show that the N- and C-terminal conserved regions of Rpb4 are involved in interaction with Rpb7, the Rpb4 interacting partner in the RNA polymerase II. We further show that the conserved N terminus is required for efficient activated transcription from the INO1 promoter but not the GAL10- or the HSE-containing promoters. The N terminus is not required for any of the stress responses tested: growth at high temperatures, sporulation, and pseudohyphal growth. The conserved C-terminal 23 amino acids are not required for the role of Rpb4 in the pseudohyphal growth phenotype but might play a role in other stress responses and activated transcription. From the deletion analysis of the non-conserved regions, we report that they influence phenotypes involving both the N and C termini (interaction with Rpb7 and transcription from the INO1 promoter) but not any of the stress-responsive phenotypes tested suggesting that they might be involved in maintaining the two conserved domains in an appropriate conformation for interaction with Rpb7 and other proteins. Taken together, our results allow us to assign phenotype-specific roles for the different conserved and non-conserved regions of Rpb4.

摘要

Rpb4是酿酒酵母中RNA聚合酶II的第四大亚基,参与多种表型,包括在高温和低温下生长、孢子形成、假菌丝生长、部分基因的激活转录以及有效的碳和能量代谢。我们通过缺失分析来确定参与这些多种表型的蛋白质结构域。scRpb4蛋白在N端和C端保守,但在中央部分有一些非保守区域。我们的缺失分析和分子建模结果表明,Rpb4的N端和C端保守区域参与了与Rpb7的相互作用,Rpb7是RNA聚合酶II中Rpb4的相互作用伙伴。我们进一步表明,保守的N端是INO1启动子高效激活转录所必需的,但不是GAL10或含热休克元件的启动子所必需的。N端对于所测试的任何应激反应都不是必需的:高温下生长、孢子形成和假菌丝生长。保守的C端23个氨基酸对于Rpb4在假菌丝生长表型中的作用不是必需的,但可能在其他应激反应和激活转录中发挥作用。从非保守区域的缺失分析中,我们报告它们影响涉及N端和C端的表型(与Rpb7的相互作用和INO1启动子的转录),但不影响所测试的任何应激反应表型,这表明它们可能参与维持两个保守结构域处于与Rpb7和其他蛋白质相互作用的合适构象。总之,我们的结果使我们能够为Rpb4的不同保守和非保守区域确定特定表型的作用。

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