Abstract
Crude cytoplasmic extracts prepared from HeLa cells actively incorporate amino acids but show little initiation of new peptides (as seen by labeling of N-terminal amino acids). In contrast, extracts prepared from cells subjected to prior inhibition of protein synthesis show a significant amount of polypeptide initiation indicated by formation of peptides with radioactive N-terminal methionine. The same result was obtained whether prior inhibition occurred with cycloheximide or by starvation for an essential amino acid. Cellular response to suppression of protein synthesis appears to be mediated through production of RNA, since it is inhibited by actinomycin but appears in the presence of cycloheximide. The crude extracts continue initiating new polypeptides for at least 10 min in vitro. It is postulated that enhancement of in vitro initiation described here is related to the apparent stimulation of initiation of translation seen in vivo.
MeSH Terms
Amino Acids/metabolism
Antibiotics, Antineoplastic/pharmacology
Cell-Free System
Cycloheximide/pharmacology
Dactinomycin/pharmacology
Female
HeLa Cells/drug effects,metabolism
Humans
Kinetics
Methionine/metabolism
Neoplasm Proteins/biosynthesis
Peptide Chain Initiation, Translational/drug effects
Sulfur Isotopes
Tritium
Chemicals
Amino Acids
Antibiotics, Antineoplastic
Neoplasm Proteins
Sulfur Isotopes
Tritium
Dactinomycin
Cycloheximide
Methionine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Reichman M
Penman S
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25 references, click to expand
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