Motohashi K, Yohda M, Endo I, Yoshida M
Research Laboratory of Resources Utilization, R-1, Tokyo Institute of Technology, Nagatsuta 4259, Yokohama 226, Japan.
J Biol Chem. 1996 Jul 19;271(29):17343-8. doi: 10.1074/jbc.271.29.17343.
We previously reported the isolation of T.DnaK.DnaJ chaperone complex from Thermus thermophilus. Here, we show that a novel factor is necessary for the assembly of T.DnaK and T.DnaJ into the complex. A dnaK gene cluster of T. thermophilus contained five genes, dnaK-grpE-dnaJ-orf4-clpB. Interestingly, T.DnaJ lacks the whole "cysteine-rich region" that has been postulated to be necessary to bind unfolded proteins. The orf4 gene encodes a novel 78-amino acid protein. Curiously, T.DnaK and T.DnaJ expressed in Escherichia coli did not form the complex. Careful reexamination of the T.DnaK.DnaJ complex revealed the presence of a small protein in the complex, which turned out to be a product of orf4. As expected, expression of three genes, dnaK-dnaJ-orf4, resulted in production of a T.DnaK.DnaJ complex in E. coli that was indistinguishable from the authentic complex in its ability to interact with nucleotide and denatured protein. The product of orf4 was also required for in vitro reconstitution of the complex and named T.DafA (T.DnaK.DnaJ assembly factor A). The complex comprises three copies each of T.DnaK, T.DnaJ, and T.DafA. Even though a definite homolog of T.DafA has not been found in the data base, this finding raises a possibility that interaction between DnaK and DnaJ chaperones in other organisms is also mediated by a small protein yet unnoticed.
我们之前报道过从嗜热栖热菌中分离出T.DnaK.DnaJ伴侣蛋白复合体。在此,我们表明一种新因子对于T.DnaK和T.DnaJ组装成该复合体是必需的。嗜热栖热菌的dnaK基因簇包含五个基因,即dnaK-grpE-dnaJ-orf4-clpB。有趣的是,T.DnaJ缺少整个据推测对于结合未折叠蛋白所必需的“富含半胱氨酸区域”。orf4基因编码一种新的78个氨基酸的蛋白质。奇怪的是,在大肠杆菌中表达的T.DnaK和T.DnaJ没有形成复合体。对T.DnaK.DnaJ复合体的仔细重新检查揭示该复合体中存在一种小蛋白,结果证明它是orf4的产物。正如预期的那样,dnaK-dnaJ-orf4这三个基因的表达导致在大肠杆菌中产生一种T.DnaK.DnaJ复合体,其与天然复合体在与核苷酸和变性蛋白相互作用的能力上没有区别。orf4的产物对于该复合体的体外重构也是必需的,并被命名为T.DafA(T.DnaK.DnaJ组装因子A)。该复合体由三个拷贝的T.DnaK、T.DnaJ和T.DafA组成。尽管在数据库中尚未发现T.DafA的确切同源物,但这一发现增加了一种可能性,即其他生物体中DnaK和DnaJ伴侣蛋白之间的相互作用也可能由一种尚未被注意到的小蛋白介导。