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

Authors
Joo, Yoo JinKim, Jin-haBaek, Joung HeeSeong, Ki MoonLee, Jae YungKim, Joon
Issue Date
11월-2009
Publisher
ELSEVIER SCIENCE BV
Keywords
Rap1p; UAS(rpg); T-rich region; Transcription factor; Ribosomal protein gene
Citation
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, v.1789, no.11-12, pp.741 - 750
Indexed
SCIE
SCOPUS
Journal Title
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS
Volume
1789
Number
11-12
Start Page
741
End Page
750
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/118991
DOI
10.1016/j.bbagrm.2009.10.002
ISSN
1874-9399
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, p 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 P-galactosidase reporter analysis and EMSA, the core promoter of RPS3 containing UAS(rpg) 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. (C) 2009 Elsevier Inc. All rights reserved.
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