YscU recognizes translocators as export substrates of the Yersinia injectisome

被引:90
作者
Sorg, Isabel
Wagner, Stefanie
Amstutz, Marlise
Mueller, Shirley A.
Broz, Petr
Lussi, Yvonne
Engel, Andreas
Cornelis, Guy R.
机构
[1] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
[2] ME Muller Inst Struct Biol, Basel, Switzerland
关键词
effectors; targeting; translocation; type III secretion; Yops;
D O I
10.1038/sj.emboj.7601731
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
YscU is an essential component of the export apparatus of the Yersinia injectisome. It consists of an N-terminal transmembrane domain and a long cytoplasmic C-terminal domain, which undergoes auto-cleavage at a NPTH site. Substitutions N263A and P264A prevented cleavage of YscU and abolished export of LcrV, YopB and YopD but not of Yop effectors. As a consequence, yscU(N263A) mutant bacteria made needles without the LcrV tip complex and they could not form translocation pores. The graft of the export signal of the effector YopE, at the N-terminus of LcrV, restored LcrV export and assembly of the tip complex. Thus, YscU cleavage is required to acquire the conformation allowing recognition of translocators, which represent an individual category of substrates in the hierarchy of export. In addition, yscUN(263A) mutant bacteria exported reduced amounts of the YscP ruler and made longer needles. Increasing YscP export resulted in needles with normal size, depending on the length of the ruler. Hence, the effect of the yscUN(263A) mutation on needle length was the consequence of a reduced YscP export.
引用
收藏
页码:3015 / 3024
页数:10
相关论文
共 53 条
[1]   Secretion of YscP from Yersinia enterocolitica is essential to control the length of the injectisome needle but not to change the type III secretion substrate specificity [J].
Agrain, C ;
Sorg, I ;
Paroz, C ;
Cornelis, GR .
MOLECULAR MICROBIOLOGY, 2005, 57 (05) :1415-1427
[2]   Characterization of a Type III secretion substrate specificity switch (T3S4) domain in YscP from Yersinia enterocolitica [J].
Agrain, C ;
Callebaut, I ;
Journet, L ;
Sorg, I ;
Paroz, C ;
Mota, LJ ;
Cornelis, GR .
MOLECULAR MICROBIOLOGY, 2005, 56 (01) :54-67
[3]   VIRG, A YERSINIA-ENTEROCOLITICA LIPOPROTEIN INVOLVED IN CA2+ DEPENDENCY, IS RELATED TO EXSB OF PSEUDOMONAS-AERUGINOSA [J].
ALLAOUI, A ;
SCHEEN, R ;
DEROUVROIT, CL ;
CORNELIS, GR .
JOURNAL OF BACTERIOLOGY, 1995, 177 (15) :4230-4237
[4]   YSCU, A YERSINIA-ENTEROCOLITICA INNER MEMBRANE-PROTEIN INVOLVED IN YOP SECRETION [J].
ALLAOUI, A ;
WOESTYN, S ;
SLUITERS, C ;
CORNELIS, GR .
JOURNAL OF BACTERIOLOGY, 1994, 176 (15) :4534-4542
[5]   Yersinia enterocolitica type III secretion:: an mRNA signal that couples translation and secretion of YopQ [J].
Anderson, DM ;
Schneewind, O .
MOLECULAR MICROBIOLOGY, 1999, 31 (04) :1139-1148
[6]   A mRNA signal for the type III secretion of Yop proteins by Yersinia enterocolitica [J].
Anderson, DM ;
Schneewind, O .
SCIENCE, 1997, 278 (5340) :1140-1143
[7]   The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes [J].
Blocker, A ;
Gounon, P ;
Larquet, E ;
Niebuhr, K ;
Cabiaux, V ;
Parsot, C ;
Sansonetti, P .
JOURNAL OF CELL BIOLOGY, 1999, 147 (03) :683-693
[8]   Structure and composition of the Shigella flexneri 'needle complex', a part of its type III secreton [J].
Blocker, A ;
Jouihri, N ;
Larquet, E ;
Gounon, P ;
Ebel, F ;
Parsot, C ;
Sansonetti, P ;
Allaoui, A .
MOLECULAR MICROBIOLOGY, 2001, 39 (03) :652-663
[9]   Role of the pilot protein YscW in the biogenesis of the YscC secretin in Yersinia enterocolitica [J].
Burghout, P ;
Beckers, F ;
de Wit, E ;
van Boxtel, R ;
Cornelis, GR ;
Tommassen, J ;
Koster, M .
JOURNAL OF BACTERIOLOGY, 2004, 186 (16) :5366-5375
[10]   TRANSCRIPTION OF THE YOP REGULON FROM Y-ENTEROCOLITICA REQUIRES TRANS ACTING PYV AND CHROMOSOMAL GENES [J].
CORNELIS, G ;
VANOOTEGEM, JC ;
SLUITERS, C .
MICROBIAL PATHOGENESIS, 1987, 2 (05) :367-379