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PMID: 9738454 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The hexokinase 2 protein participates in regulatory DNA-protein complexes necessary for glucose repression of the SUC2 gene in Saccharomyces cerevisiae.

FEBS letters ·Vol. 434 ·No. 1-2 ·1998-08-28 ·Pages 71-6

Herrero P, Martínez-Campa C, Moreno F

Abstract

The HXK2 gene plays an important role in glucose repression in the yeast Saccharomyces cerevisiae. Recently we have described that the HXK2 gene product, isoenzyme 2 of hexokinase, is located both in the nucleus and in the cytoplasm of S. cerevisiae cells. In this work we used deletion analysis to identify the essential part of the protein-mediating nuclear localisation. Determinations of fructose-kinase activity and immunoblot analysis using anti-Hxk2 antibodies in isolated nuclei, together with observations of the fluorescence distribution of Hxk2-GFP fusion protein in cells transformed with an HXK2::gfp mutant gene, indicated that the decapeptide KKPQARKGSM, located between amino acid residues 7 and 16 of hexokinase 2, is important for nuclear localisation of the protein. Further experimental evidence, measuring invertase activity in wild-type and mutant cells expressing a truncated version of the Hxk2 protein unable to enter the nucleus, shows that a nuclear localisation of Hxk2 is necessary for glucose repression signalling of the SUC2 gene. Furthermore, we demonstrate using gel mobility shift analysis that Hxk2 participates in DNA-protein complexes with cis-acting regulatory elements of the SUC2 gene promoter.

MeSH Terms
Amino Acid Sequence DNA, Fungal/genetics,metabolism Gene Expression Regulation, Fungal/drug effects Glucose/pharmacology Glycoside Hydrolases/genetics,metabolism Hexokinase/metabolism Molecular Sequence Data Mutation Protein Binding Saccharomyces cerevisiae/genetics,metabolism beta-Fructofuranosidase
Chemicals
DNA, Fungal Hexokinase Glycoside Hydrolases beta-Fructofuranosidase Glucose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Herrero P
Departamento de Bioquímica y Biologia Molecular, Instituto Universitario de Biotecnología de Asturias, Universidad de Oviedo, Spain.
Martínez-Campa C
Moreno F
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1998-08-28
Pages
71-6
Language
English
Region
England
NLM ID
0155157
Subset
IM
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