Literature DB >> 6646128

Programmed macromolecular synthesis in regenerating karyoplasts.

J D White, J Bruno, J J Lucas.   

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.

Mesh:

Year:  1983        PMID: 6646128      PMCID: PMC370048          DOI: 10.1128/mcb.3.10.1866-1881.1983

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  29 in total

1.  Identification and characterization of multiple forms of actin.

Authors:  J I Garrels; W Gibson
Journal:  Cell       Date:  1976-12       Impact factor: 41.582

2.  High resolution two-dimensional electrophoresis of proteins.

Authors:  P H O'Farrell
Journal:  J Biol Chem       Date:  1975-05-25       Impact factor: 5.157

3.  The construction of viable nuclear-cytoplasmic hybrid cells by nuclear transplantation.

Authors:  J J Lucas; J R Kates
Journal:  Cell       Date:  1976-03       Impact factor: 41.582

4.  The regeneration and division of mouse L-cell karyoplasts.

Authors:  J J Lucas; E Szekely; J R Kates
Journal:  Cell       Date:  1976-01       Impact factor: 41.582

5.  Isolation and preliminary characterization of 10-nm filaments from baby hamster kidney (BHK-21) cells.

Authors:  J M Starger; R D Goldman
Journal:  Proc Natl Acad Sci U S A       Date:  1977-06       Impact factor: 11.205

6.  The surface morphology and fine structure of CHO (Chinese hamster ovary) cells following enucleation.

Authors:  J W Shay; K R Porter; D M Prescott
Journal:  Proc Natl Acad Sci U S A       Date:  1974-08       Impact factor: 11.205

7.  Reconstruction of mammalian cells from nuclear and cytoplasmic components separated by treatment with cytochalasin B.

Authors:  G Veomett; D M Prescott; J Shay; K R Porter
Journal:  Proc Natl Acad Sci U S A       Date:  1974-05       Impact factor: 11.205

8.  A low-viscosity epoxy resin embedding medium for electron microscopy.

Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

9.  Enucleation of mammalian cells with cytochalasin B.

Authors:  D M Prescott; D Myerson; J Wallace
Journal:  Exp Cell Res       Date:  1972       Impact factor: 3.905

10.  Characterization of minicells (nuclei) obtained by cytochalasin enucleation.

Authors:  T Ege; H Hamberg; U Krondahl; J Ericsson; N R Ringertz
Journal:  Exp Cell Res       Date:  1974-08       Impact factor: 3.905

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  1 in total

1.  Transient correction of genetic defects in cultured animal cells by introduction of functional proteins.

Authors:  D Ortiz; M M Baldwin; J J Lucas
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

  1 in total

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