Abstract
1. DNA prepared from non-gelable rat liver nuclei isolated in the presence of disrupted mitochondria at pH 6.0, has been compared with DNA obtained from gelable nuclei isolated at pH 4.0. The DNA of the non-gelable nuclei is partially depolymerized relative to the DNA of the gelable nuclei. 2. It has been found that sufficiently small quantities of crystallized DNAase I can cleave a very large part of the DNA of gelable nuclei isolated at pH 4 from the residual protein of these nuclei without causing extensive depolymerization of the DNA. At the same time the gelable nuclei are rendered non-gelable. 3. Partially purified DNAase II can also render gelable nuclei isolated at pH 4 non-gelable, and in so doing presumably also cleaves the DNA from the residual protein of the nuclei. 4. Mitochondrial DNAase I appears to be the enzyme responsible to a large extent for the cleavage of DNA from the residual protein of gelable rat liver cell nuclei with concomitant destruction of the gel-forming capability of these nuclei, when the nuclei are subjected to the action of disrupted mitochondria at pH 6.0 during the isolation procedure. 5. Mitochondrial DNAase II does not appear to exert appreciable action on nuclei during the course of isolation of the nuclei at pH 6.0 in the presence of disrupted mitochondria. 6. It is probable that DNAase I is not the sole enzyme responsible for destroying the gelability of nuclei isolated at pH 6.0 in the presence of disrupted mitochondria. Protease may be involved. 7. Sodium dodecyl sulfate at pH 6.0–6.3 cleaves the DNA of isolated gelable nuclei from the residual protein of these nuclei over a period of 2 to 3 hours. At pH 7.0–7.5, however, there is negligible cleavage over a period of 96 hours. 8. If non-gelable nuclei are isolated at pH 6.0 in the presence of disrupted mitochondria, DNA subsequently can be removed from them by the use of detergent at pH values ranging from 6.0–7.5 without the necessity of incubation in the detergent solution, since the DNA had already been detached from the residual protein by the action of the mitochondrial enzyme system during isolation of the nuclei.
Full Text
The Full Text of this article is available as a PDF (717.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bernstein M. H. OBSERVATIONS ON THE STRUCTURE OF DEOXYRIBONUCLEOPROTEIN GELS. Proc Natl Acad Sci U S A. 1956 Oct;42(10):703–707. doi: 10.1073/pnas.42.10.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DE DUVE C., PRESSMAN B. C., GIANETTO R., WATTIAUX R., APPELMANS F. Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue. Biochem J. 1955 Aug;60(4):604–617. doi: 10.1042/bj0600604. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DOUNCE A. L., MONTY K. J. Factors influencing the ability of isolated cell nuclei to from gels in dilute alkali. J Biophys Biochem Cytol. 1955 Mar;1(2):155–160. doi: 10.1083/jcb.1.2.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DOUNCE A. L., WITTER R. F., MONTY K. J., PATE S., COTTONE M. A. A method for isolating intact mitochondria and nuclei from the same homogenate, and the influence of mitochondrial destruction on the properties of cell nuclei. J Biophys Biochem Cytol. 1955 Mar;1(2):139–153. doi: 10.1083/jcb.1.2.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ENGBRING V. K., LASKOWSKI M. Protein components of chicken erythrocyte nuclei. Biochim Biophys Acta. 1953 Jun;11(2):244–251. doi: 10.1016/0006-3002(53)90033-x. [DOI] [PubMed] [Google Scholar]
- GOUTIER-PIROTTE M., OTH A. Dégélification des noyaux et activité nucléasique. Biochim Biophys Acta. 1956 Nov;22(2):394–396. doi: 10.1016/0006-3002(56)90169-x. [DOI] [PubMed] [Google Scholar]
- IRVIN E. M., IRVIN J. L., ROTHERHAM J., SCHOTTELIUS D. D. The deoxyribonuclease of rat liver in relation to the isolation of deoxyribonucleoprotein. J Biol Chem. 1956 Dec;223(2):817–829. [PubMed] [Google Scholar]
- KIELLEY W. W., KIELLEY R. K. Myokinase and adenosinetriphosphatase in oxidative phosphorylation. J Biol Chem. 1951 Aug;191(2):485–500. [PubMed] [Google Scholar]
- KOWLESSAR O. D., ALTMAN K. I., HEMPELMANN L. H. The effect of ionizing radiation on deoxyribonuclease activities of body fluids. I. The effect of total body exposure on the urinary excretion of deoxyribonucleases. Arch Biochem Biophys. 1954 Oct;52(2):362–372. doi: 10.1016/0003-9861(54)90136-8. [DOI] [PubMed] [Google Scholar]
- Sumner J. B. A METHOD FOR THE COLORIMETRIC DETERMINATION OF PHOSPHORUS. Science. 1944 Nov 3;100(2601):413–414. doi: 10.1126/science.100.2601.413. [DOI] [PubMed] [Google Scholar]
