Signal transduction pathways in response to protein misfolding in the extracytoplasmic compartments of E-coli: Role of two new phosphoprotein phosphatases PrpA and PrpB

被引:88
作者
Missiakas, D
Raina, S
机构
[1] UNIV GENEVA, CTR MED, DEPT BIOCHIM MED, CH-1211 GENEVA 4, SWITZERLAND
[2] CNRS, CTR BIOCHIM & BIOL MOL, LIDSM, F-13402 MARSEILLE 20, FRANCE
关键词
cpxR cpxA operon; E-coli extracytoplasm; phosphoprotein phosphatases; protein misfolding; rpoE regulon;
D O I
10.1093/emboj/16.7.1670
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is now well established that the sigma(E) regulon of Escherichia coli is induced by misfolding of proteins in the periplasm and the outer membrane, htrA belongs to this regulon and encodes a periplasmic protease involved in the degradation of misfolded proteins. htrA transcription is also under the positive control of a two component signal transduction system CpxR CpxA. Closer examination of the putative signal transduction pathway modulating htrA transcription has led us to the identification of two new genes, Biochemical and genetic evidence shows that these two genes encode two phosphoprotein phosphatases, designated PrpA and PrpB. These are the first examples of typical serine/threonine and tyrosine phosphatases described in E,coli, PrpA and PrpB are involved in signaling protein misfolding via the CpxR CpxA transducing system. In addition, both PrpA and PrpB modulate the phosphorylated status of some other phosphoproteins in E.coli. Finally, we show that PrpA is a heat shock protein.
引用
收藏
页码:1670 / 1685
页数:16
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