Jenkins A J, March J B, Oliver I R, Masters M
Mol Gen Genet. 1986 Mar;202(3):446-54. doi: 10.1007/BF00333275.
An 8.2 kb fragment of E. coli chromosomal DNA, when cloned in increased copy number, suppresses the dnaA46 mutation, and an abundant protein of about 68 kd (60 kd when measured by us), encoded by the fragment, is essential for the suppression (Takeda and Hirota 1982). Mapping experiments show that the fragment originates from the 94 min region of the chromosome. It encodes several proteins but only one abundant polypeptide of the correct size, the product of the groEL gene. Suppression by the fragment is allele specific; those mutations which map to the centre of the gene are suppressed. Other initiation mutants including dnaA203, dnaA204, dnaA508, dnaAam, dnaC, dnaP and dnaB252 are not suppressed. Most suppressed strains are cold-sensitive suggesting an interaction between the mutant proteins (or their genes) and the suppressing protein or proteins.
当以增加的拷贝数进行克隆时,一段8.2 kb的大肠杆菌染色体DNA片段可抑制dnaA46突变,该片段编码的一种约68 kd(我们测定为60 kd)的丰富蛋白质对于这种抑制作用至关重要(武田和广田,1982年)。定位实验表明,该片段起源于染色体的94分钟区域。它编码几种蛋白质,但只有一种大小合适的丰富多肽,即groEL基因的产物。该片段的抑制作用具有等位基因特异性;那些定位于基因中心的突变会被抑制。其他起始突变体,包括dnaA203、dnaA204、dnaA508、dnaAam、dnaC、dnaP和dnaB252则不会被抑制。大多数被抑制的菌株对温度敏感,这表明突变蛋白(或其基因)与抑制蛋白之间存在相互作用。