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细胞表面蛋白基因 ecm33+ 是两个转录因子 Atf1 和 Mbx1 的靶点,负调控裂殖酵母中 Pmk1 MAPK 细胞完整性信号通路。

The cell surface protein gene ecm33+ is a target of the two transcription factors Atf1 and Mbx1 and negatively regulates Pmk1 MAPK cell integrity signaling in fission yeast.

机构信息

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.

出版信息

Mol Biol Cell. 2010 Feb 15;21(4):674-85. doi: 10.1091/mbc.e09-09-0810. Epub 2009 Dec 23.

DOI:10.1091/mbc.e09-09-0810
PMID:20032302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2820430/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/f171feb6b6b6/zmk0041093560008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/bdee3d81d079/zmk0041093560001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/8e2135256d5f/zmk0041093560002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/da0bdf98fffe/zmk0041093560003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/e943b8dfba01/zmk0041093560004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/646d952fb5e0/zmk0041093560005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/872c5d323d1b/zmk0041093560006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/619f0ca2b22f/zmk0041093560007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/f171feb6b6b6/zmk0041093560008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/bdee3d81d079/zmk0041093560001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/8e2135256d5f/zmk0041093560002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/da0bdf98fffe/zmk0041093560003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/e943b8dfba01/zmk0041093560004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/646d952fb5e0/zmk0041093560005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/872c5d323d1b/zmk0041093560006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/619f0ca2b22f/zmk0041093560007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/2820430/f171feb6b6b6/zmk0041093560008.jpg

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