Sorg Isabel, Wagner Stefanie, Amstutz Marlise, Müller Shirley A, Broz Petr, Lussi Yvonne, Engel Andreas, Cornelis Guy R
Infection Biology, Biozentrum der Universität Basel, Klingelbergstrasse 50-70, CH 4056 Basel, Switzerland.
EMBO J. 2007 Jun 20;26(12):3015-24. doi: 10.1038/sj.emboj.7601731. Epub 2007 May 17.
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, yscU(N263A) 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 yscU(N263A) mutation on needle length was the consequence of a reduced YscP export.
YscU是耶尔森氏菌注射体输出装置的一个必需组件。它由一个N端跨膜结构域和一个长的胞质C端结构域组成,该C端结构域在一个NPTH位点发生自切割。N263A和P264A替换阻止了YscU的切割,并消除了LcrV、YopB和YopD的输出,但不影响Yop效应蛋白的输出。因此,yscU(N263A)突变细菌形成了没有LcrV尖端复合物的针状结构,并且它们无法形成转运孔。将效应蛋白YopE的输出信号嫁接到LcrV的N端,恢复了LcrV的输出和尖端复合物的组装。因此,YscU切割是获得允许识别转运蛋白的构象所必需的,转运蛋白在输出层次结构中代表一类单独的底物。此外,yscU(N263A)突变细菌输出的YscP标尺数量减少,形成了更长的针状结构。根据标尺的长度,增加YscP的输出会导致针状结构尺寸正常。因此,yscU(N263A)突变对针状结构长度的影响是YscP输出减少的结果。