Laboratory of Molecular Pharmacogenomics, Laboratory of Molecular and Cellular Biology, and Laboratory of Bioinformatics, School of Pharmaceutical Sciences, Kinki University, Higashi-Osaka, 577-8502, Japan.
Mol Biol Cell. 2010 Feb 15;21(4):674-85. doi: 10.1091/mbc.e09-09-0810. Epub 2009 Dec 23.
The highly conserved fission yeast Pmk1 MAPK pathway plays a key role in cell integrity by regulating Atf1, which belongs to the ATF/cAMP-responsive element-binding (CREB) protein family. We identified and characterized ecm33(+), which encodes a glycosyl-phosphatidylinositol (GPI)-anchored cell surface protein as a transcriptional target of Pmk1 and Atf1. We demonstrated that the gene expression of Ecm33 is regulated by two transcription factors Atf1 and a MADS-box-type transcription factor Mbx1. We identified a putative ATF/CREB-binding site and an RLM1-binding site in the ecm33(+) promoter region and monitored the transcriptional activity of Atf1 or Mbx1 in living cells using a destabilized luciferase reporter gene fused to three tandem repeats of the CRE and six tandem repeats of the Rlm1-binding sequence, respectively. These reporter genes reflect the activation of the Pmk1 pathway by various stimuli, thereby enabling the real-time monitoring of the Pmk1 cell integrity pathway. Notably, the Deltaecm33 cells displayed hyperactivation of the Pmk1 signaling together with hypersensitivity to Ca(2+) and an abnormal morphology, which were almost abolished by simultaneous deletion of the components of the Rho2/Pck2/Pmk1 pathway. Our results suggest that Ecm33 is involved in the negative feedback regulation of Pmk1 cell integrity signaling and is linked to cellular Ca(2+) signaling.
高度保守的裂殖酵母 Pmk1 MAPK 途径通过调节属于 ATF/cAMP 反应元件结合(CREB)蛋白家族的 Atf1,在细胞完整性中发挥关键作用。我们鉴定并表征了 ecm33(+),它编码一种糖基磷脂酰肌醇(GPI)锚定的细胞表面蛋白,是 Pmk1 和 Atf1 的转录靶标。我们证明 Ecm33 的基因表达受两个转录因子 Atf1 和一个 MADS 盒型转录因子 Mbx1 调节。我们在 ecm33(+)启动子区域中鉴定了一个假定的 ATF/CREB 结合位点和一个 RLM1 结合位点,并使用融合了三个串联重复的 CRE 和六个串联重复的 Rlm1 结合序列的不稳定荧光素酶报告基因,分别在活细胞中监测 Atf1 或 Mbx1 的转录活性。这些报告基因反映了各种刺激下 Pmk1 途径的激活,从而能够实时监测 Pmk1 细胞完整性途径。值得注意的是,Deltaecm33 细胞表现出 Pmk1 信号的过度激活,同时对 Ca(2+)敏感和形态异常,这些异常几乎可以通过同时删除 Rho2/Pck2/Pmk1 途径的成分来消除。我们的结果表明,Ecm33 参与 Pmk1 细胞完整性信号的负反馈调节,并与细胞 Ca(2+)信号有关。