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doi:10.1534/genetics.106.059766
A more recent version of this article appeared on October 1, 2006.
REGULAR RESEARCH PAPERS |
Connection between the Rag4 glucose sensor and the KlRgt1 repressor in Kluyveromyces lactis
Stéphane Rolland 1, Martina Hnatova 2, Marc Lemaire 2, Juana Leal-Sanchez 3 and Micheline Wesolowski-Louvel 2*
1 Dartmouth Medical School, Genetics Department, Hanover, NH 03755
2 UMR5122/CNRS/UCBL/INSA
3 Institute of Signaling, Developmental Biology and Cancer Research, Centre Lacassagne
* To whom correspondence should be addressed. E-mail: louvel{at}univ-lyon1.fr.
Submitted on April 21, 2006
Revised on May 22, 2006
Accepted on 1 June 2006
The RAG4 gene encodes for the sole transmembrane glucose sensor of Kluyveromyces lactis. A rag4 mutation leads to a fermentation-deficient phenotype (Rag- phenotype) and to a severe defect in the expression of the major glucose transporter gene RAG1. A recessive extragenic suppressor of the rag4 mutation has been identified. It encodes a protein (KlRgt1) 31% identical to the Saccharomyces cerevisiae Rgt1 regulator of the HXT genes (ScRgt1). The Klrgt1 null mutant displays abnormal high levels of RAG1 expression in the absence of glucose but still presents an induction of RAG1 expression in the presence of glucose. KlRgt1 is therefore only a repressor of RAG1. As described for ScRgt1, the KlRgt1 repressor function is controlled by phosphorylation in response to high glucose concentration and this phosphorylation is dependent on the sensor Rag4 and the casein kinase Rag8. However, contrary to that observed with ScRgt1, KlRgt1 is always bound to the RAG1 promoter. This study reveals that the key components of the glucose signaling pathway are conserved between S. cerevisiae and K. lactis, but points out major differences in Rgt1 regulation and function, that might reflect different carbon metabolism of these yeasts.
Key Words: K. lactis, glucose transport, regulation of transcription, yeast
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