CNF1 exploits the ubiquitin-proteasome machinery to restrict Rho GTPase activation for bacterial host cell invasion

被引:241
作者
Doye, A
Mettouchi, A
Bossis, G
Clément, R
Buisson-Touati, C
Flatau, G
Gagnoux, L
Piechaczyk, M
Boquet, P
Lemichez, E
机构
[1] Fac Med, INSERM, U452, IFR 50, F-06107 Nice, France
[2] Fac Med, INSERM, U3825, IFR 50, F-06107 Nice, France
[3] Ctr Antoine Lacassagne, CNRS, UMR 6543, IFR 72, F-06189 Nice, France
[4] Inst Genet Mol, CNRS, UMR 5535, IFR 24, F-34293 Montpellier, France
关键词
D O I
10.1016/S0092-8674(02)01132-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
CNF1 toxin is a virulence factor produced by uropathogenic Escherichia coli. Upon cell binding and introduction into the cytosol, CNF1 deamidates glutamine 63 of RhoA (or 61 of Rac and Cdc42), rendering constitutively active these GTPases. Unexpectedly, we measured in bladder cells a transient CNF1-induced activation of Rho GTPases, maximal for Rac. Deactivation of Rac correlated with the increased susceptibility of its deamidated form to ubiquitin/proteasome-mediated degradation. Sensitivity to ubiquitylation could be generalized to other permanent-activated forms of Rac and to its sustained activation by Dbl. Degradation of the toxin-activated Rac allowed both host cell motility and efficient cell invasion by uropathogenic bacteria. CNF1 toxicity thus results from a restricted activation of Rho GTPases through hijacking the host cell proteasomal machinery.
引用
收藏
页码:553 / 564
页数:12
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