Donovan W P, Kushner S R
Proc Natl Acad Sci U S A. 1986 Jan;83(1):120-4. doi: 10.1073/pnas.83.1.120.
The isolation of a temperature-sensitive allele of RNase II (rnb) by in vitro mutagenesis has permitted the demonstration that RNase II and polynucleotide phosphorylase (PNPase) are required for cell viability and mRNA turnover in Escherichia coli. Double-mutant strains carrying the pnp-7 and rnb-500 alleles (PNPase deficient and RNase II thermolabile) ceased growing in Luria broth within 30 min after shift to the nonpermissive temperature. Cessation of growth was accompanied by an accumulation of mRNA fragments 100-1500 nucleotides long. In contrast, single-mutant and wild-type control strains grew normally at the nonpermissive temperature and did not accumulate mRNA. No significant changes in rRNA patterns were observed in any of the strains.
通过体外诱变分离出核糖核酸酶II(RNase II,rnb)的温度敏感等位基因,这使得人们能够证明,核糖核酸酶II和多核苷酸磷酸化酶(PNPase)是大肠杆菌细胞存活和信使核糖核酸(mRNA)周转所必需的。携带pnp-7和rnb-500等位基因的双突变菌株(PNPase缺陷型和RNase II热不稳定型)在转移到非允许温度后30分钟内,在Luria肉汤中停止生长。生长停止伴随着长度为100 - 1500个核苷酸的mRNA片段的积累。相比之下,单突变和野生型对照菌株在非允许温度下正常生长,且不积累mRNA。在任何菌株中均未观察到核糖体核糖核酸(rRNA)模式的显著变化。