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来自海拉细胞的特定RNA切割活性。

Specific RNA-cleaving activities from HeLa cells.

作者信息

Ferrari S, Yehle C O, Robertson H D, Dickson E

出版信息

Proc Natl Acad Sci U S A. 1980 May;77(5):2395-9. doi: 10.1073/pnas.77.5.2395.

Abstract

Subcellular fractionation of HeLa cells was carried out under gentle conditions to isolate enzymes that cleave RNA precursors in a specific manner. Four separate activities--cleavage of HeLa cell heterogeneous nuclear RNA, the HeLa cell 45S rRNA precursor, RNA . DNA hybrids (RNase H), and the Escherichia coli tRNATyr precursor (RNase P)--were revealed by these studies. The specificity and limited nature of these cleavages suggest that they are due to eukaryotic RNA-processing enzymes. The virtual absence of random nucleases from these enzymes was demonstrated by their inability to cleave the 8000-base early mRNA precursor of bacteriophage T7, E. coli 30S rRNA precursor, or HeLa cytoplasmic poly(A)-containing RNA.

摘要

在温和条件下对HeLa细胞进行亚细胞分级分离,以分离出能以特定方式切割RNA前体的酶。这些研究揭示了四种不同的活性——HeLa细胞核不均一RNA的切割、HeLa细胞45S rRNA前体的切割、RNA·DNA杂交体(核糖核酸酶H)以及大肠杆菌tRNATyr前体(核糖核酸酶P)的切割。这些切割的特异性和有限性质表明它们是由真核生物RNA加工酶引起的。这些酶几乎不存在随机核酸酶,这一点通过它们无法切割噬菌体T7的8000碱基早期mRNA前体、大肠杆菌30S rRNA前体或HeLa细胞质中含聚腺苷酸的RNA得到了证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a2a/349405/284f053d2448/pnas00492-0052-a.jpg

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