Abstract
Conditions for the preparation, purification, and maintenance of karyoplasts which could regenerate to reform whole viable cells were defined. Results of biochemical analyses of such karyoplasts at various times during regeneration indicated that a reproducible biosynthetic program was followed. Thus, an examination of the polypeptides made during regeneration by two-dimensional gel electrophoresis showed that the pattern of radiolabeled polypeptides synthesized at each time studied was specific and was significantly different from that observed at other times during regeneration. Polypeptides associated with three major cellular fractions--nuclear, cytoskeletal-microtrabecular, and soluble--were among the most dramatically regulated molecules. Other polypeptides, such as the major components of microfilaments and intermediate filaments, were synthesized at relatively constant rates and were assembled into structures throughout regeneration. Likewise, microtubules appeared to be reformed throughout regeneration, even in the absence of identifiable centriole-associated organizing centers. Finally, analysis of DNA synthesis by autoradiography showed that, even when prepared from whole cells synchronized at the G1/S interface, karyoplasts could not begin making DNA until they had regenerated an almost complete complement of cytoplasm.
Full text
PDF















Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bravo R., Celis J. E. A search for differential polypeptide synthesis throughout the cell cycle of HeLa cells. J Cell Biol. 1980 Mar;84(3):795–802. doi: 10.1083/jcb.84.3.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown R. L., Papenfuss C. M. DNA synthesis in permeabilized karyoplasts from cytochalasin B-enucleated mouse L cells. Exp Cell Res. 1981 Apr;132(2):478–482. doi: 10.1016/0014-4827(81)90125-7. [DOI] [PubMed] [Google Scholar]
- Brown R. L., Wible L. J., Brinkley B. R. Cytoplasmic microtubule assembly-disassembly in enucleated cells and regenerating karyoplasts. Cell Biol Int Rep. 1980 May;4(5):453–458. doi: 10.1016/0309-1651(80)90032-6. [DOI] [PubMed] [Google Scholar]
- Bruno J., Reich N., Lucas J. J. Globin synthesis in hybrid cells constructed by transplantation of dormant avian erythrocyte nuclei into enucleated fibroblasts. Mol Cell Biol. 1981 Dec;1(12):1163–1176. doi: 10.1128/mcb.1.12.1163. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ege T., Hamberg H., Krondahl U., Ericsson J., Ringertz N. R. Characterization of minicells (nuclei) obtained by cytochalasin enucleation. Exp Cell Res. 1974 Aug;87(2):365–377. doi: 10.1016/0014-4827(74)90493-5. [DOI] [PubMed] [Google Scholar]
- Garrels J. I., Gibson W. Identification and characterization of multiple forms of actin. Cell. 1976 Dec;9(4 Pt 2):793–805. doi: 10.1016/0092-8674(76)90142-2. [DOI] [PubMed] [Google Scholar]
- Garrels J. I., Schubert D. Modulation of protein synthesis by nerve growth factor. J Biol Chem. 1979 Aug 25;254(16):7978–7985. [PubMed] [Google Scholar]
- Garrels J. I. Two dimensional gel electrophoresis and computer analysis of proteins synthesized by clonal cell lines. J Biol Chem. 1979 Aug 25;254(16):7961–7977. [PubMed] [Google Scholar]
- Ivarie R. D., O'Farrell P. H. The glucocorticoid domain: steroid-mediated changes in the rate of synthesis of rat hepatoma proteins. Cell. 1978 Jan;13(1):41–55. doi: 10.1016/0092-8674(78)90136-8. [DOI] [PubMed] [Google Scholar]
- Lenk R., Penman S. The cytoskeletal framework and poliovirus metabolism. Cell. 1979 Feb;16(2):289–301. doi: 10.1016/0092-8674(79)90006-0. [DOI] [PubMed] [Google Scholar]
- Lipsich L. A., Lucas J. J., Kates J. R. Cell cycle dependence of the reactivation of chick erythrocyte nuclei after transplantation into mouse L929 cell cytoplasts. J Cell Physiol. 1978 Nov;97(2):199–207. doi: 10.1002/jcp.1040970209. [DOI] [PubMed] [Google Scholar]
- Lucas J. J., Kates J. R. The construction of viable nuclear-cytoplasmic hybrid cells by nuclear transplantation. Cell. 1976 Mar;7(3):397–405. doi: 10.1016/0092-8674(76)90169-0. [DOI] [PubMed] [Google Scholar]
- Lucas J. J., Szekely E., Kates J. R. The regeneration and division of mouse L-cell karyoplasts. Cell. 1976 Jan;7(1):115–122. doi: 10.1016/0092-8674(76)90261-0. [DOI] [PubMed] [Google Scholar]
- Lucas J. J., Zorn G. A., Brings A., Szekely E., Kates J. R. Recent developments with karyoplast regeneration and nuclear transplantation. Natl Cancer Inst Monogr. 1978 May;(48):37–44. [PubMed] [Google Scholar]
- Milcarek C., Zahn K. The synthesis of ninety proteins including actin throughout the HeLa cell cycle. J Cell Biol. 1978 Dec;79(3):833–838. doi: 10.1083/jcb.79.3.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
- O'Farrell P. Z., Goodman H. M., O'Farrell P. H. High resolution two-dimensional electrophoresis of basic as well as acidic proteins. Cell. 1977 Dec;12(4):1133–1141. doi: 10.1016/0092-8674(77)90176-3. [DOI] [PubMed] [Google Scholar]
- Prescott D. M., Myerson D., Wallace J. Enucleation of mammalian cells with cytochalasin B. Exp Cell Res. 1972;71(2):480–485. doi: 10.1016/0014-4827(72)90322-9. [DOI] [PubMed] [Google Scholar]
- Sharp G. A., Osborn M., Weber K. Ultrastructure of multiple microtubule initiation sites in mouse neuroblastoma cells. J Cell Sci. 1981 Feb;47:1–24. doi: 10.1242/jcs.47.1.1. [DOI] [PubMed] [Google Scholar]
- Shay J. W., Porter K. R., Prescott D. M. The surface morphology and fine structure of CHO (Chinese hamster ovary) cells following enucleation. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3059–3063. doi: 10.1073/pnas.71.8.3059. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Small J. V., Celis J. E. Direct visualization of the 10-nm (100-A)-filament network in whole and enucleated cultured cells. J Cell Sci. 1978 Jun;31:393–409. doi: 10.1242/jcs.31.1.393. [DOI] [PubMed] [Google Scholar]
- Spurr A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res. 1969 Jan;26(1):31–43. doi: 10.1016/s0022-5320(69)90033-1. [DOI] [PubMed] [Google Scholar]
- Starger J. M., Goldman R. D. Isolation and preliminary characterization of 10-nm filaments from baby hamster kidney (BHK-21) cells. Proc Natl Acad Sci U S A. 1977 Jun;74(6):2422–2426. doi: 10.1073/pnas.74.6.2422. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steinberg R. A., Coffino P. Two-dimensional gel analysis of cyclic AMP effects in cultured S49 mouse lymphoma cells: protein modifications, inductions and repressions. Cell. 1979 Nov;18(3):719–733. doi: 10.1016/0092-8674(79)90126-0. [DOI] [PubMed] [Google Scholar]
- Tucker R. W., Pardee A. B., Fujiwara K. Centriole ciliation is related to quiescence and DNA synthesis in 3T3 cells. Cell. 1979 Jul;17(3):527–535. doi: 10.1016/0092-8674(79)90261-7. [DOI] [PubMed] [Google Scholar]
- Tucker R. W., Scher C. D., Stiles C. D. Centriole deciliation associated with the early response of 3T3 cells to growth factors but not to SV40. Cell. 1979 Dec;18(4):1065–1072. doi: 10.1016/0092-8674(79)90219-8. [DOI] [PubMed] [Google Scholar]
- Veomett G., Prescott D. M., Shay J., Porter K. R. Reconstruction of mammalian cells from nuclear and cytoplasmic components separated by treatment with cytochalasin B. Proc Natl Acad Sci U S A. 1974 May;71(5):1999–2002. doi: 10.1073/pnas.71.5.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- XEROS N. Deoxyriboside control and synchronization of mitosis. Nature. 1962 May 19;194:682–683. doi: 10.1038/194682a0. [DOI] [PubMed] [Google Scholar]
- Zorn G. A., Lucas J. J., Kates J. R. Purification and characterization of regenerating mouse L929 karyoplasts. Cell. 1979 Nov;18(3):659–672. doi: 10.1016/0092-8674(79)90121-1. [DOI] [PubMed] [Google Scholar]








