Abstract |
In a search for eucaryotic enzymes which might process the heterogenous nuclear RNA ( HnRNA) from animal cells into messenger RNA, a ribonuclease called RNAse D analogous to E. coli RNAse III in its ability to cleave specifically synthetic or viral double-stranded polyribonucleotides has been detected and extensively purified from the cytosol of Krebs II mouse ascites cells. The purification procedure involved cellular fractionation followed by DEAE-and CM- cellulose chromatography and resulted in an RNAas D preparation contaminated with trace amounts of single-strand specific RNAse (equivalent to less than 0.3 ng per ml) as assayed against poly (rC). Significant levels of RNAse H activity against poly (rA)- poly (dT) were still present in these preparations.
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Authors | J Rech, G Cathala, P Jeanteur |
Journal | Nucleic acids research
(Nucleic Acids Res)
Vol. 3
Issue 8
Pg. 2055-65
(Aug 1976)
ISSN: 0305-1048 [Print] England |
PMID | 967689
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Animals
- Carcinoma, Krebs 2
(enzymology)
- Cell Nucleus
- Kinetics
- Mice
- Ribonucleases
(isolation & purification, metabolism)
- Subcellular Fractions
(enzymology)
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