RRC ID 35127
Author Numamoto M, Tagami S, Ueda Y, Imabeppu Y, Sasano Y, Sugiyama M, Maekawa H, Harashima S.
Title Nuclear localization domains of GATA activator Gln3 are required for transcription of target genes through dephosphorylation in Saccharomyces cerevisiae.
Journal J Biosci Bioeng
Abstract The GATA transcription activator Gln3 in the budding yeast (Saccharomyces cerevisiae) activates transcription of nitrogen catabolite repression (NCR)-sensitive genes. In cells grown in the presence of preferred nitrogen sources, Gln3 is phosphorylated in a TOR-dependent manner and localizes in the cytoplasm. In cells grown in non-preferred nitrogen medium or treated with rapamycin, Gln3 is dephosphorylated and is transported from the cytoplasm to the nucleus, thereby activating the transcription of NCR-sensitive genes. Caffeine treatment also induces dephosphorylation of Gln3 and its translocation to the nucleus and transcription of NCR-sensitive genes. However, the details of the mechanism by which phosphorylation controls Gln3 localization and transcriptional activity are unknown. Here, we focused on two regions of Gln3 with nuclear localization signal properties (NLS-K, and NLS-C) and one with nuclear export signal (NES). We constructed various mutants for our analyses: gln3 containing point mutations in all potential phosphoacceptor sites (Thr-339, Ser-344, Ser-347, Ser-355, Ser-391) in the NLS and NES regions to produce non-phosphorylatable (alanine) or mimic-phosphorylatable (aspartic acid) residues; and deletion mutants. We found that phosphorylation of Gln3 was impaired in all of these mutations and that the aspartic acid substitution mutants showed drastic reduction of Gln3-mediated transcriptional activity despite the fact that the mutations had no effect on nuclear localization of Gln3. Our observations suggest that these regions are required for transcription of target genes presumably through dephosphorylation.
Volume 120(2)
Pages 121-7
Published 2015-8
DOI 10.1016/j.jbiosc.2014.12.017
PII S1389-1723(14)00497-6
PMID 25641578
MeSH Amino Acid Sequence Amino Acid Substitution Aspartic Acid / genetics Caffeine / pharmacology Cell Nucleus / drug effects Cell Nucleus / metabolism* Cytoplasm / metabolism Gene Expression Regulation, Fungal* / drug effects Molecular Sequence Data Nitrogen / metabolism Nuclear Export Signals / genetics Nuclear Localization Signals / chemistry Nuclear Localization Signals / genetics Phosphorylation / drug effects Phosphorylation / genetics Point Mutation Protein Structure, Tertiary Protein Transport / drug effects Protein Transport / genetics Saccharomyces cerevisiae / cytology Saccharomyces cerevisiae / drug effects Saccharomyces cerevisiae / genetics* Saccharomyces cerevisiae / metabolism* Saccharomyces cerevisiae Proteins / chemistry* Saccharomyces cerevisiae Proteins / genetics Saccharomyces cerevisiae Proteins / metabolism* Sirolimus / pharmacology Transcription Factors / chemistry* Transcription Factors / genetics Transcription Factors / metabolism* Transcription, Genetic* / drug effects Transcriptional Activation / drug effects
IF 2.032
Times Cited 2
WOS Category BIOTECHNOLOGY & APPLIED MICROBIOLOGY FOOD SCIENCE & TECHNOLOGY
Resource
Yeast NA