Jung U S, Levin D E
Department of Biochemistry and Molecular Biology, School of Public Health, The Johns Hopkins University, 615 N. Wolfe Street, Baltimore, MD 21205, USA.
Mol Microbiol. 1999 Dec;34(5):1049-57. doi: 10.1046/j.1365-2958.1999.01667.x.
The cell integrity pathway of Saccharomyces cerevisiae monitors cell wall remodelling during growth and differentiation. Additionally, this pathway responds to environmental stresses that challenge the integrity of the cell wall. We conducted a genome-wide survey of genes whose expression was altered in response to activation of Mpk1/Slt2, the MAP kinase, under the control of cell integrity signalling. We identified 25 genes whose regulation was altered by Mpk1 activity. Among these, 20 were positively regulated by Mpk1, and five were negatively regulated. Most of the genes identified encode either known or suspected cell wall proteins or enzymes involved in cell wall biogenesis. These include glycosyl-phosphatidylinositol (GPI) proteins, members of the Pir family of cell wall proteins, Mpk1 itself and others. All of the regulation detected was mediated by the Rlm1 transcription factor, a MADS-box protein that is phosphorylated and activated by Mpk1, but for which no transcriptional targets had been identified. A similar pattern of regulation was observed when cell integrity signalling was induced by environmental stress (i.e. temperature upshift).
酿酒酵母的细胞完整性途径在生长和分化过程中监测细胞壁重塑。此外,该途径对挑战细胞壁完整性的环境压力作出反应。我们对在细胞完整性信号控制下,其表达因MAP激酶Mpk1/Slt2激活而改变的基因进行了全基因组调查。我们鉴定出25个其调控因Mpk1活性而改变的基因。其中,20个受Mpk1正调控,5个受负调控。鉴定出的大多数基因编码已知或疑似的细胞壁蛋白或参与细胞壁生物合成的酶。这些包括糖基磷脂酰肌醇(GPI)蛋白、细胞壁蛋白Pir家族成员、Mpk1本身等。检测到的所有调控均由Rlm1转录因子介导,Rlm1是一种MADS盒蛋白,被Mpk1磷酸化并激活,但尚未鉴定出其转录靶点。当通过环境压力(即温度升高)诱导细胞完整性信号时,观察到类似的调控模式。