Petersen S K, Hansen F G
Department of Microbiology, Technical University of Denmark, Lyngby-Copenhagen.
J Bacteriol. 1991 Aug;173(16):5200-6. doi: 10.1128/jb.173.16.5200-5206.1991.
An RNA polymerase mutant with a single-base-pair change in the rpoC gene affects chromosome initiation control. The mutation, which is recessive, is a G to A transition leading to the substitution of aspartate for glycine at amino acid residue 1033 in the RNA polymerase beta' subunit. The chromosome copy number is increased twofold in the mutant at semipermissive growth temperatures (39 degrees C). In a delta oriC strain, in which chromosome initiation is governed by an F replicon, chromosome copy number is not affected. Plasmid pBR322 copy number is also increased in the mutant at 39 degrees C. The mutation causes a more than fivefold increased expression of the dnaA gene at 39 degrees C. It is conceivable that it is this high DnaA concentration which causes the high chromosome copy number and that the mutant RNA polymerase beta' subunit exerts its effect by altering the expression of the dnaA gene. However, other factors must be affected as well to explain why the RNA polymerase mutant can grow in a balanced fashion with a high chromosome concentration. This is in contrast to wild-type cells, which exhibit higher origin concentrations when DnaA protein is overproduced, but in which the overall DNA concentration is only moderately affected.
一种在rpoC基因中有单碱基对变化的RNA聚合酶突变体影响染色体起始控制。该突变是隐性的,是从G到A的转变,导致RNA聚合酶β'亚基中第1033位氨基酸残基处的甘氨酸被天冬氨酸取代。在半允许生长温度(39℃)下,突变体中的染色体拷贝数增加了两倍。在染色体起始由F复制子控制的δoriC菌株中,染色体拷贝数不受影响。在39℃时,突变体中质粒pBR322的拷贝数也增加。该突变导致在39℃时dnaA基因的表达增加了五倍以上。可以想象,正是这种高浓度的DnaA导致了高染色体拷贝数,并且突变的RNA聚合酶β'亚基通过改变dnaA基因的表达发挥其作用。然而,为了解释为什么RNA聚合酶突变体能够以高染色体浓度以平衡的方式生长,其他因素也必须受到影响。这与野生型细胞形成对比,当DnaA蛋白过量产生时,野生型细胞表现出更高的起始浓度,但其中总体DNA浓度仅受到适度影响。