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PMID: 2046672 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Protein synthesis requirements for nuclear division, cytokinesis, and cell separation in Saccharomyces cerevisiae.

Molecular and cellular biology ·Vol. 11 ·No. 7 ·1991-07-00 ·Pages 3691-8

Burke DJ, Church D

Abstract

Protein synthesis inhibitors have often been used to identify regulatory steps in cell division. We used cell division cycle mutants of the yeast Saccharomyces cerevisiae and two chemical inhibitors of translation to investigate the requirements for protein synthesis for completing landmark events after the G1 phase of the cell cycle. We show, using cdc2, cdc6, cdc7, cdc8, cdc17 (38 degrees C), and cdc21 (also named tmp1) mutants, that cells arrested in S phase complete DNA synthesis but cannot complete nuclear division if protein synthesis is inhibited. In contrast, we show, using cdc16, cdc17 (36 degrees C), cdc20, cdc23, and nocodazole treatment, that cells that arrest in the G2 stage complete nuclear division in the absence of protein synthesis. Protein synthesis is required late in the cell cycle to complete cytokinesis and cell separation. These studies show that there are requirements for protein synthesis in the cell cycle, after G1, that are restricted to two discrete intervals.

MeSH Terms
Cell Cycle/drug effects Cell Division/drug effects Cell Nucleus/drug effects,ultrastructure Cycloheximide/pharmacology DNA Replication/drug effects Fungal Proteins/biosynthesis Genotype S Phase/drug effects Saccharomyces cerevisiae/drug effects,growth & development,metabolism Trichodermin/pharmacology
Chemicals
Fungal Proteins Trichodermin Cycloheximide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Burke D J
Department of Biology, University of Virginia, Charlottesville 22901.
Church D
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39 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1991-07-00
Pages
3691-8
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC361131
Subset
IM
Grants
NIGMS NIH HHS · GM 40334-02 · United States
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