A ribonuclease which degrades RNA specifically in RNA. DNA hybrid structures has been purified 1500 fold from Escherichia coli B and 200 fold from E. coli strain D110 pol A1, endo I-, thy-). For maximal activity, the enzyme requires Mg(2+) and the presence of a sulfhydryl reagent. The enzyme is capable of digesting more than 95% of the RNA in RNA.DNA hybrids to acid soluble products. The products are oligonucleotides with 5' phosphate and 3' hydroxyl termini. The enzyme acts as an endonuclease and does not require free 3' or 5' termini for activity. However, it cannot cleave the phosphodiester bond covalently linking ribonucleotides to DNA. With circular single stranded DNA templates deoxynucleotide incorporation catalyzed by DNA polymerase II is dependent on RNA synthesis. This reaction can be stimulated by RNase H. During these studies an additional ribonuclease H activity was detected in E. coli B and purified 160 fold. Unlike RNase H, this activity is N ethylmaleimide resistant and sensitive to antiserum prepared against DNA polymerase I and attacks [3' 3H,5' 32P]poly(A) poly(dT) in the 5'→ 3' direction.
|Original language||English (US)|
|Number of pages||8|
|Journal||Journal of Biological Chemistry|
|State||Published - 1973|
ASJC Scopus subject areas
- Molecular Biology
- Cell Biology