Sato Akane, Kimura Takumi, Hondo Kana, Kawano-Kawada Miyuki, Sekito Takayuki
Laboratory of Molecular Physiology and Genetics, Faculty of Agriculture, Ehime University, Matsuyama, Ehime, Japan.
Proteo-Science Center (PROS), Ehime University, Matsuyama, Ehime, Japan.
Biosci Biotechnol Biochem. 2021 Feb 24;85(3):587-599. doi: 10.1093/bbb/zbaa041.
In Saccharomyces cerevisiae, Avt4 exports neutral and basic amino acids from vacuoles. Previous studies have suggested that the GATA transcription factors, Gln3 and Gat1, which are key regulators that adapt cells in response to changes in amino acid status, are involved in the AVT4 transcription. Here, we show that mutations in the putative GATA-binding sites of the AVT4 promoter reduced AVT4 expression. Consistently, a chromatin immunoprecipitation (ChIP) assay revealed that Gat1-Myc13 binds to the AVT4 promoter. Previous microarray results were confirmed that gln3∆gat1∆ cells showed a decrease in expression of AVT1 and AVT7, which also encode vacuolar amino acid transporters. Additionally, ChIP analysis revealed that the AVT6 encoding vacuolar acidic amino acid exporter represents a new direct target of the GATA transcription factor. The broad effect of the GATA transcription factors on the expression of AVT transporters suggests that vacuolar amino acid transport is integrated into cellular amino acid homeostasis.
在酿酒酵母中,Avt4从液泡中输出中性和碱性氨基酸。先前的研究表明,GATA转录因子Gln3和Gat1是使细胞适应氨基酸状态变化的关键调节因子,参与AVT4的转录。在此,我们表明AVT4启动子推定的GATA结合位点发生突变会降低AVT4的表达。一致地,染色质免疫沉淀(ChIP)分析表明Gat1-Myc13与AVT4启动子结合。先前的微阵列结果得到证实,gln3∆gat1∆细胞中AVT1和AVT7的表达下降,这两种基因也编码液泡氨基酸转运蛋白。此外,ChIP分析表明,编码液泡酸性氨基酸转运蛋白的AVT6是GATA转录因子的一个新的直接靶点。GATA转录因子对AVT转运蛋白表达的广泛影响表明,液泡氨基酸转运被整合到细胞氨基酸稳态中。