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丝裂原活化蛋白激酶(MAP激酶)和环磷酸腺苷(cAMP)丝状化信号通路汇聚于酵母FLO11基因异常大的启动子上。

MAP kinase and cAMP filamentation signaling pathways converge on the unusually large promoter of the yeast FLO11 gene.

作者信息

Rupp S, Summers E, Lo H J, Madhani H, Fink G

机构信息

Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA.

出版信息

EMBO J. 1999 Mar 1;18(5):1257-69. doi: 10.1093/emboj/18.5.1257.

Abstract

In Saccharomyces cerevisiae, two major signal transduction pathways, the Kss1 MAPK pathway and the cAMP-regulated pathway, are critical for the differentiation of round yeast form cells to multicellular, invasive pseudohyphae. Here we report that these parallel pathways converge on the promoter of a gene, FLO11, which encodes a cell surface protein required for pseudohyphal formation. The FLO11 promoter is unusually large, containing at least four upstream activation sequences (UASs) and nine repression elements which together span at least 2.8 kb. Several lines of evidence indicate that the MAPK and cAMP signals are received by distinct transcription factors and promoter elements. First, regulation via the MAPK pathway requires the transcription factors Ste12p/Tec1p, whereas cAMP-mediated activation requires a distinct factor, Flo8p. Secondly, mutations in either pathway block FLO11 transcription. Overexpression of STE12 can suppress the loss of FLO8, and overexpression of FLO8 can suppress the loss of STE12. Finally, multiple distinct promoter regions of the FLO11 promoter are required for its activation by either Flo8p or Ste12p/ Tec1p. Thus, like the promoters of the key developmental genes, HO and IME1, the FLO11 promoter is large and complex, endowing it with the ability to integrate multiple inputs.

摘要

在酿酒酵母中,两条主要的信号转导途径,即Kss1丝裂原活化蛋白激酶(MAPK)途径和环磷酸腺苷(cAMP)调节途径,对于圆形酵母细胞分化为多细胞的侵袭性假菌丝至关重要。在此,我们报告这些平行途径汇聚于一个基因FLO11的启动子,该基因编码假菌丝形成所需的一种细胞表面蛋白。FLO11启动子异常大,包含至少四个上游激活序列(UASs)和九个抑制元件,它们共同跨越至少2.8 kb。几条证据表明,MAPK和cAMP信号由不同的转录因子和启动子元件接收。首先,通过MAPK途径的调控需要转录因子Ste12p/Tec1p,而cAMP介导的激活需要一个不同的因子Flo8p。其次,任一途径中的突变都会阻断FLO11转录。STE12的过表达可抑制FLO8的缺失,FLO8的过表达可抑制STE12的缺失。最后,Flo8p或Stel2p/Tec1p激活FLO11启动子需要多个不同的启动子区域。因此,与关键发育基因HO和IME1的启动子一样,FLO11启动子大且复杂,使其具备整合多种输入信号的能力。

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