Koski R A, Bothwell A L, Altman S
Cell. 1976 Sep;9(1):101-16. doi: 10.1016/0092-8674(76)90056-8.
An endoribonuclease which cleaves tRNA precursor molecules has been partially purified from human KB tissue culture cells. This activity is found in cytoplasmic fractions but is not detectable in the nucleoplasm. tRNA precursor molecules from both E. coli and KB cells are cleaved by this novel activity to produce 5' phosphate-terminated oligonucleotides. E coli RNAase P and the KB cell nuclease both make a single endonucleolytic scission in E. coli tRNATyr precursor, thereby separating the 41 extra nucleotides on the 5' end of the precursor molecule from the 5' terminal sequence of the mature tRNATyr molecule. The cleavage products generated from other E. coli tRNA precursors by the KB cell activity are identical in size to those produced by RNAase P. The KB cell endoribonuclease requires Mg2+ and a monovalent cation (Na+, K+, or NH4+) for function. The enzymatic activity has a broad pH optimum, centered near pH 8.0, and the activity is inhibited by tRNA. Several KB cell RNAs with long half-lives in vivo, including 5S and bulk 4S RNA, are not cleaved by this nuclease. The KB cell endoribonuclease resembles E. coli RNAase P in its substrate specificity, pH optimum, ion requirements, and sensitivity to tRNA. These properties and the cytoplasmic localization of the novel endoribonuclease indicate its involvement in the biosynthesis of KB cell tRNA.
一种能切割tRNA前体分子的核糖核酸内切酶已从人KB组织培养细胞中部分纯化出来。这种活性存在于细胞质组分中,但在核质中检测不到。来自大肠杆菌和KB细胞的tRNA前体分子都能被这种新活性切割,产生5'磷酸末端的寡核苷酸。大肠杆菌核糖核酸酶P和KB细胞核酸酶都在大肠杆菌tRNATyr前体中进行一次内切核酸酶切割,从而将前体分子5'端的41个额外核苷酸与成熟tRNATyr分子的5'末端序列分开。KB细胞活性对其他大肠杆菌tRNA前体产生的切割产物在大小上与核糖核酸酶P产生的产物相同。KB细胞核糖核酸内切酶发挥功能需要Mg2+和一价阳离子(Na+、K+或NH4+)。该酶活性在pH接近8.0时具有较宽的最佳pH值,并且其活性受到tRNA的抑制。几种在体内半衰期较长的KB细胞RNA,包括5S和大量4S RNA,不会被这种核酸酶切割。KB细胞核糖核酸内切酶在底物特异性、最佳pH值、离子需求以及对tRNA的敏感性方面类似于大肠杆菌核糖核酸酶P。这些特性以及这种新型核糖核酸内切酶的细胞质定位表明它参与了KB细胞tRNA的生物合成。