The rat liver nucleolus, after fragmentation induced by ethionine treatment, has been found to undergo complete reformation by adenine in the presence of a dose of cycloheximide sufficient to cause inhibition of protein synthesis by 90–95%. In contrast, actinomycin D given along with adenine was followed by the appearance of a small compact mass containing only the fibrillar component with no evident granules. This structure resembled pseudonucleoli seen in the anucleolate mutant of Xenopus laevis or in certain early stages of amphibian oocytes. Actinomycin D administered 2 hr after adenine induced a segregation of the fibrillar and granular components of nucleoli similar to that induced in the normal nucleolus. The implications of these findings in relation to nucleolar organization are briefly discussed.
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1 April 1969
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April 01 1969
REFORMATION OF NUCLEOLI AFTER ETHIONE-INDUCED FRAGMENTATION IN THE ABSENCE OF SIGNIFICANT PROTEIN SYNTHESIS
Hisashi Shinozuka,
Hisashi Shinozuka
From the Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213
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Emmanuel Farber
Emmanuel Farber
From the Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213
Search for other works by this author on:
Hisashi Shinozuka
From the Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213
Emmanuel Farber
From the Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213
Received:
October 02 1968
Revision Received:
November 11 1968
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1969 by The Rockefeller University Press.
1969
J Cell Biol (1969) 41 (1): 280–286.
Article history
Received:
October 02 1968
Revision Received:
November 11 1968
Citation
Hisashi Shinozuka, Emmanuel Farber; REFORMATION OF NUCLEOLI AFTER ETHIONE-INDUCED FRAGMENTATION IN THE ABSENCE OF SIGNIFICANT PROTEIN SYNTHESIS . J Cell Biol 1 April 1969; 41 (1): 280–286. doi: https://doi.org/10.1083/jcb.41.1.280
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