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酿酒酵母RPS3基因核心启动子区域的测定

Determination of the core promoter regions of the Saccharomyces cerevisiae RPS3 gene.

作者信息

Joo Yoo Jin, Kim Jin-Ha, Baek Joung Hee, Seong Ki Moon, Lee Jae Yung, Kim Joon

机构信息

Labotoray of Biochemistry, School of Life Sciences and Biotechnology, and BioInsititute, Korea University, Seoul 136-701, Korea.

出版信息

Biochim Biophys Acta. 2009 Nov-Dec;1789(11-12):741-50. doi: 10.1016/j.bbagrm.2009.10.002. Epub 2009 Oct 22.

Abstract

Ribosomal protein genes (RPG), which are scattered throughout the genomes of all eukaryotes, are subjected to coordinated expression. In yeast, the expression of RPGs is highly regulated, mainly at the transcriptional level. Recent research has found that many ribosomal proteins (RPs) function in multiple processes in addition to protein synthesis. Therefore, detailed knowledge of promoter architecture as well as gene regulation is important in understanding the multiple cellular processes mediated by RPGs. In this study, we investigated the functional architecture of the yeast RPS3 promoter and identified many putative cis-elements. Using beta-galactosidase reporter analysis and EMSA, the core promoter of RPS3 containing UASrpg and T-rich regions was corroborated. Moreover, the promoter occupancy of RPS3 by three transcription factors was confirmed. Taken together, our results further the current understanding of the promoter architecture and trans-elements of the Saccharomyces cerevisiae RPS3 gene.

摘要

核糖体蛋白基因(RPG)分布于所有真核生物的基因组中,其表达受到协同调控。在酵母中,RPG的表达受到高度调控,主要在转录水平。最近的研究发现,许多核糖体蛋白(RP)除了参与蛋白质合成外,还在多个过程中发挥作用。因此,详细了解启动子结构以及基因调控对于理解RPG介导的多种细胞过程至关重要。在本研究中,我们研究了酵母RPS3启动子的功能结构,并鉴定了许多假定的顺式元件。通过β-半乳糖苷酶报告基因分析和电泳迁移率变动分析(EMSA),证实了包含UASrpg和富含T区域的RPS3核心启动子。此外,还证实了三种转录因子对RPS3启动子的占据。综上所述,我们的结果进一步加深了目前对酿酒酵母RPS3基因启动子结构和反式元件的理解。

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