Abstract
1. The loss of nucleic acids and protein from isolated HeLa-cell nuclei was studied. During 4hr. incubation at 37° DNA was conserved, but appreciable amounts of RNA and protein were lost. 2. Two classes of nuclear RNA were distinguished: at least 75% of the RNA was lost from the nuclei relatively slowly through degradation to acid-soluble fragments; the rest of the RNA was lost much more rapidly, not only through degradation to acid-soluble fragments but also through diffusion of RNA out of the nuclei into the incubation medium. 3. The RNA that was preferentially lost was the fraction of nuclear RNA that was rapidly labelled when intact HeLa cells were grown in a medium containing radioactive precursors of RNA. 4. The RNA appearing in the incubation medium was apparently partially degraded and had a sedimentation coefficient of about that of transfer RNA. 5. Both the degradation of RNA and the loss of RNA from the nuclei were sensitive to bivalent cations. Low concentrations of Mg2+ and Mn2+ greatly increased the rate of degradation of the rapidly labelled RNA to acid-soluble fragments, and produced a corresponding decrease in the amount of RNA diffusing into the medium. At higher concentrations they suppressed both degradation and diffusion of RNA. The cations Ca2+, Cu2+, Zn2+ and Ni2+ all progressively inhibited both forms of loss of RNA. 6. Salts of univalent cations produced appreciable effects only at ionic strengths of about 0·2, when degradation to acid-soluble fragments was preferentially inhibited. 7. Both ADP and ATP inhibited loss of RNA at about 30mm. 8. It was concluded that the diffusion of rapidly labelled RNA out of the isolated nuclei was not related to the movement of RNA from nucleus to cytoplasm in vivo, but reflected the ease with which the rapidly labelled RNA detached from the chromatin and the permeability of the membranes of isolated nuclei.
Full text
PDF








Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adams D. H. The relationship between cellular nucleic acids in the developing rat cerebral cortex. Biochem J. 1966 Feb;98(2):636–640. doi: 10.1042/bj0980636. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Attardi G., Parnas H., Hwang M. I., Attardi B. Giant-size rapidly labeled nuclear ribonucleic acid and cytoplasmic messenger ribonucleic acid in immature duck erythrocytes. J Mol Biol. 1966 Sep;20(1):145–182. doi: 10.1016/0022-2836(66)90123-9. [DOI] [PubMed] [Google Scholar]
- BURTON K. A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J. 1956 Feb;62(2):315–323. doi: 10.1042/bj0620315. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bramwell M. E., Harris H. The origin of the polydispersity in sedimentation patterns of rapidly labelled nuclear ribonucleic acid. Biochem J. 1967 Jun;103(3):816–830. doi: 10.1042/bj1030816. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GOLDBERG I. H. Ribonucleic acid synthesis in nuclear extracts of mammalian cells grown in suspension culture; effect of ionic strength and surface-active agents. Biochim Biophys Acta. 1961 Jul 22;51:201–204. doi: 10.1016/0006-3002(61)91042-3. [DOI] [PubMed] [Google Scholar]
- HARRIS H. Turnover of nuclear and cytoplasmic ribonucleic acid in two types of animal cell, with some further observations on the nucleolus. Biochem J. 1959 Oct;73:362–369. doi: 10.1042/bj0730362. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lazarus H. M., Sporin M. B. Purification and properties of a nuclear exoribonuclease from Ehrlich ascites tumor cells. Proc Natl Acad Sci U S A. 1967 May;57(5):1386–1393. doi: 10.1073/pnas.57.5.1386. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PHILIPSON L. Chromatographic separation, and characteristics of nucleic acids from HeLa cells. J Gen Physiol. 1961 May;44:899–910. doi: 10.1085/jgp.44.5.899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roberts W. K. Studies on RNA synthesis in Ehrlich ascites cells extraction and properties of labeled RNA. Biochim Biophys Acta. 1965 Nov 8;108(3):474–488. doi: 10.1016/0005-2787(65)90039-0. [DOI] [PubMed] [Google Scholar]
- SALZMAN N. P. Systematic fluctuations in the cellular protein, RNA and DNA during growth of mammalian cell cultures. Biochim Biophys Acta. 1959 Jan;31(1):158–163. doi: 10.1016/0006-3002(59)90451-2. [DOI] [PubMed] [Google Scholar]
- Soeiro R., Birnboim H. C., Darnell J. E. Rapidly labeled HeLa cell nuclear RNA. II. Base composition and cellular localization of a heterogeneous RNA fraction. J Mol Biol. 1966 Aug;19(2):362–372. doi: 10.1016/s0022-2836(66)80010-4. [DOI] [PubMed] [Google Scholar]
- Watts J. W., Davis M. A. The effect of proflavine on HeLa cells. Biochem J. 1966 Aug;100(2):467–472. doi: 10.1042/bj1000467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watts J. W. Turnover of nucleic acids in a multiplying animal cell. 1. Incorporation studies. Biochem J. 1964 Nov;93(2):297–305. doi: 10.1042/bj0930297. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watts J. W. Turnover of nucleic acids in a multiplying animal cell. 2. Retention studies. Biochem J. 1964 Nov;93(2):306–312. doi: 10.1042/bj0930306. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Widnell C. C., Tata J. R. Studies on the stimulation by ammonium sulphate of the DNA-dependent RNA polymerase of isolated rat-liver nuclei. Biochim Biophys Acta. 1966 Sep;123(3):478–492. doi: 10.1016/0005-2787(66)90216-4. [DOI] [PubMed] [Google Scholar]
- Wiesner R., Acs G., Reich E., Shafiq A. Degradation of ribonucleic acid in mouse fibroblasts treated with actinomycin. J Cell Biol. 1965 Oct;27(1):47–52. doi: 10.1083/jcb.27.1.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
