Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25893
Title: Mutations in GCR1 affect SUC2 gene expression in Saccharomyces cerevisiae
Authors: Turgut, T.
Lopez, Maria Cecilia
Uemura, Hiroshi
Baker, Henry V.
Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.
Türkel, Sezai
AAH-6281-2021
7003319075
Keywords: Biochemistry and molecular biology
Genetics and heredity
Eukaryota
Saccharomyces cerevisiae
SUC2
Invertase
GCR1
Glucose repression
Repressor-activator protein-1
Glucose repression
Transcriptional activation
Chromatin-structure
Messenger-RNAS
Yeast
Promoter
Binding
Sequence
SNF
Issue Date: Mar-2003
Publisher: Springer Heidelberg
Citation: Türkel, S. vd. (2003). “Mutations in GCR1 affect SUC2 gene expression in Saccharomyces cerevisiae”. Molecular Genetics and Genomics, 268(6), 825-831.
Abstract: Transcription of SUC2, the gene that encodes the cytoplasmic and secreted forms of the enzyme invertase, is controlled by glucose repression and derepression mechanisms in Saccharomyces cerevisiae. Several regulatory factors such as the Mig1p-Tup1p-Ssn6p repressor complex and the Snf1p kinase complex have been identified previously as regulators of SUC2 expression. We show that, in addition to these factors, expression of SUC2 is affected by mutations in the gene GCR1 that encodes the glycolysis regulatory protein Gcr1p. Expression of Suc2-LacZ was not repressed by glucose in gcr1 mutant yeast cells exposed to glucose. Furthermore, secreted invertase activity was constitutively expressed under glucose-repressed and derepressed conditions in gcr1 mutants. DNA gel mobility shift assays and in-vitro DNase I protection experiments mapped a DNA binding site for Ger1p in the transcriptional control region of the SUC2 gene, next to a previously mapped Mig1p binding site. However, the mechanism by which gcr1 mutations relieve glucose repression remains obscure.
URI: https://doi.org/10.1007/s00438-003-0808-4
https://link.springer.com/article/10.1007/s00438-003-0808-4
http://hdl.handle.net/11452/25893
ISSN: 1617-4615
Appears in Collections:PubMed
Scopus
Web of Science

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