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PMID: 5057977 Published · ppublish English Journal Article

The synthesis of acidic chromosomal proteins during the cell cycle of HeLa S-3 cells. II. The kinetics of residual protein synthesis and transport.

The Journal of cell biology ·Vol. 52 ·No. 2 ·1972-02-00 ·Pages 308-15

Borun TW, Stein GS

Abstract

The kinetics of acidic residual chromosomal protein synthesis and transport were studied throughout the cell cycle in HeLa S-3 cells synchronized by 2 mM thymidine block and selective detachment of mitotic cells. Pulse labeling the cells with leucine-(3)H for 2 min and then "chasing" the radioactive proteins for up to 3 hr showed that the amount of protein synthesized, transported, and retained in the acidic residual chromosomal protein fraction is greater immediately after mitosis and later in G(1) than in the S or G(2) phases of the cell cycle. During S, only 20-25% of the proteins synthesized and transported to the acidic residual chromosomal protein fraction are chased during the first 2 hr after pulse labeling, whereas up to 40% of the material entering the residual nuclear fraction in mitosis, G(1), and G(2) leaves during a 2 hr chase. Polyacrylamide gel electrophoretic profiles of these proteins, at various times after pulse labeling, reveal that the turnover of individual polypeptides within this fraction has kinetics of synthesis and turnover which are markedly different from one another and undergo stage-specific changes.

MeSH Terms
Electrophoresis, Disc HeLa Cells/metabolism Kinetics Leucine/metabolism Mitosis Nucleoproteins/analysis,biosynthesis,metabolism Proteins/analysis Thymidine/metabolism Time Factors Tritium
Chemicals
Nucleoproteins Proteins Tritium Leucine Thymidine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Borun T W
Stein G S
References (15)
15 references, click to expand
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1972-02-00
Pages
308-15
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2108627
Subset
IM
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