Mhammedi-Alaoui A, Pato M, Gama M J, Toussaint A
Unité Transposition Bactérienne, Université Libre de Bruxelles, Rhode St Genèse, Belgium.
Mol Microbiol. 1994 Mar;11(6):1109-16. doi: 10.1111/j.1365-2958.1994.tb00387.x.
We have shown previously that some particular mutations in bacteriophage Mu repressor, the frameshift vir mutations, made the protein very sensitive to the Escherichia coli ATP-dependent Clp protease. This enzyme is formed by the association between a protease subunit (ClpP) and an ATPase subunit. ClpA, the best characterized of these ATPases, is not required for the degradation of the mutant Mu repressors. Recently, a new potential ClpP associated ATPase, ClpX, has been described. We show here that this new subunit is required for Mu vir repressor degradation. Moreover, ClpX (but not ClpP) was found to be required for normal Mu replication. Thus ClpX has activities that do not require its association with ClpP. In the pathway of Mu replicative transposition, the block resides beyond the strand transfer reaction, i.e. after the transposition reaction per se is completed, suggesting that ClpX is required for the transition to the formation of the active replication complex at one Mu end. This is a new clear-cut case of the versatile activity of polypeptides that form multi-component ATP-dependent proteases.
我们之前已经表明,噬菌体Mu阻遏物中的一些特定突变,即移码vir突变,会使该蛋白质对大肠杆菌ATP依赖的Clp蛋白酶非常敏感。这种酶由一个蛋白酶亚基(ClpP)和一个ATP酶亚基结合形成。这些ATP酶中研究得最清楚的ClpA,对于突变型Mu阻遏物的降解并非必需。最近,一种新的潜在的与ClpP相关的ATP酶ClpX被描述出来。我们在此表明,这个新亚基是Mu vir阻遏物降解所必需的。此外,发现正常的Mu复制需要ClpX(而不是ClpP)。因此,ClpX具有一些不需要其与ClpP结合的活性。在Mu复制性转座途径中,阻断发生在链转移反应之后,即在转座反应本身完成之后,这表明ClpX是在一个Mu末端向形成活性复制复合体转变过程中所必需的。这是形成多组分ATP依赖蛋白酶的多肽具有多种活性的一个新的明确例子。