Nakada N, Yoshinaga K, Ishihama A, Nagasawa-Fujimori H
Mol Gen Genet. 1982;188(2):173-8. doi: 10.1007/BF00332671.
On exposure to high temperature of a temperature-sensitive RNA polymerase beta' subunit (rpoC92) mutant of Escherichia coli, selective reduction was observed in the rate of synthesis of a group of proteins including RNA polymerase beta' subunit. The finding that the synthesis of beta' subunit but not beta subunit was specifically repressed in this mutant grown at non-permissive temperature indicates that the functionally intact RNA polymerase is required for the synthesis of beta beta' subunits be coordinated. In addition, the assembly of newly synthesized RNA polymerase subunits was inefficient in this mutant at the steps where altered beta' subunit was involved, and the unassembled enzyme subunits were rapidly and preferentially degraded. During recovery to non-restricted growth, the synthesis of both beta and beta' subunits was transiently enhanced in parallel leading to recovery of the intracellular concentration of functional RNA polymerase.
将大肠杆菌的温度敏感型RNA聚合酶β'亚基(rpoC92)突变体暴露于高温下时,观察到包括RNA聚合酶β'亚基在内的一组蛋白质的合成速率出现选择性降低。在非允许温度下生长的该突变体中,β'亚基而非β亚基的合成受到特异性抑制,这一发现表明,ββ'亚基的合成协调需要功能完整的RNA聚合酶。此外,在涉及改变的β'亚基的步骤中,该突变体中新合成的RNA聚合酶亚基组装效率低下,未组装的酶亚基迅速且优先降解。在恢复到不受限制的生长过程中,β和β'亚基的合成同时短暂增强,导致功能性RNA聚合酶的细胞内浓度恢复。