Two independent type III secretion mechanisms for YopE in Yersinia enterocolitica

被引:164
|
作者
Cheng, LW
Anderson, DM
Schneewind, O
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT MICROBIOL & IMMUNOL,LOS ANGELES,CA 90095
[2] UNIV CALIF LOS ANGELES,SCH MED,INST MOL BIOL,LOS ANGELES,CA 90095
关键词
GRAM-NEGATIVE BACTERIA; CHAPERONE-LIKE PROTEIN; TRANSPOSON TN5; TARGET-CELL; GENE; DETERMINANTS; EXPRESSION; RESISTANCE; MUTATIONS; SELECTION;
D O I
10.1046/j.1365-2958.1997.3831750.x
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
Pathogenic Yersinia species escape the infected host's defense mechanisms by targeting cytotoxic Yop proteins into the cytoplasm of macrophages via a type III secretion pathway. Two separate secretion signals contained in YopE were identified, each of which were sufficient but not necessary for the secretion of reporter molecules. One signal is located within the coding sequence of the first 15 amino acids and is sufficient for the secretion of fusion proteins but not required for YopE secretion. The second signal is located downstream at residues 15-100 of YopE and is only recognized by the type III machinery when it is bound to SycE. We propose the existence of two independent mechanisms that allow for the secretion of Yap proteins.
引用
收藏
页码:757 / 765
页数:9
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