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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-16024

Ferreira, T C; Hertzberg, L; Gassmann, M; Campos, E G (2007). The yeast genome may harbor hypoxia response elements (HRE). Comparative Biochemistry and Physiology - Part C: Toxicology & Pharmacology, 146(1-2):255-263.

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Abstract

The hypoxia-inducible factor-1 (HIF-1) is a heterodimeric transcription factor activated when cells are submitted to hypoxia. The heterodimer is composed of two subunits, HIF-1alpha and the constitutively expressed HIF-1beta. During normoxia, HIF-1alpha is degraded by the 26S proteasome, but hypoxia causes HIF-1alpha to be stabilized, enter the nucleus and bind to HIF-1beta, thus forming the active complex. The complex then binds to the regulatory sequences of various genes involved in physiological and pathological processes. The specific regulatory sequence recognized by HIF-1 is the hypoxia response element (HRE) that has the consensus sequence 5'BRCGTGVBBB3'. Although the basic transcriptional regulation machinery is conserved between yeast and mammals, Saccharomyces cerevisiae does not express HIF-1 subunits. However, we hypothesized that baker's yeast has a protein analogous to HIF-1 which participates in the response to changes in oxygen levels by binding to HRE sequences. In this study we screened the yeast genome for HREs using probabilistic motif search tools. We described 24 yeast genes containing motifs with high probability of being HREs (p-value<0.1) and classified them according to biological function. Our results show that S. cerevisiae may harbor HREs and indicate that a transcription factor analogous to HIF-1 may exist in this organism.

Item Type:Journal Article, refereed, original work
Communities & Collections:05 Vetsuisse Faculty > Institute of Veterinary Physiology
04 Faculty of Medicine > Center for Integrative Human Physiology
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:August 2007
Deposited On:22 Mar 2009 12:13
Last Modified:27 Nov 2013 20:15
Publisher:Elsevier
ISSN:1532-0456
Publisher DOI:10.1016/j.cbpc.2006.08.013
PubMed ID:17035097
Citations:Web of Science®. Times Cited: 6
Google Scholar™
Scopus®. Citation Count: 8

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