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Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids

Chinese hamster ovary (CHO) cells were subjected to severe amino acid starvation for histidine, leucine, methionine, asparagine, tyrosine, glutamine, valine, and lysine, using amino acid analogs or mutations in specific aminoacyl-tRNA synthetases. At protein synthetic rates of less than 5%, in all c...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113223/
https://www.ncbi.nlm.nih.gov/pubmed/6715412
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collection PubMed
description Chinese hamster ovary (CHO) cells were subjected to severe amino acid starvation for histidine, leucine, methionine, asparagine, tyrosine, glutamine, valine, and lysine, using amino acid analogs or mutations in specific aminoacyl-tRNA synthetases. At protein synthetic rates of less than 5%, in all cases, the newly synthesized proteins were found on two- dimensional electrophoretic gels to consist of a few intensely labeled spots, with the exception of lysine. This pattern could also be produced by strong inhibition of cytoplasmic protein synthesis with cycloheximide, and was abolished by preincubation with the mitochondrial protein synthesis inhibitor chloramphenicol. It appears therefore that the spots represent mitochondrial protein synthesis and that animal cells must have separate aminoacyl-tRNA synthetases for mitochondrial tRNAs corresponding to all these amino acids except, possibly, for lysine.
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spelling pubmed-21132232008-05-01 Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids J Cell Biol Articles Chinese hamster ovary (CHO) cells were subjected to severe amino acid starvation for histidine, leucine, methionine, asparagine, tyrosine, glutamine, valine, and lysine, using amino acid analogs or mutations in specific aminoacyl-tRNA synthetases. At protein synthetic rates of less than 5%, in all cases, the newly synthesized proteins were found on two- dimensional electrophoretic gels to consist of a few intensely labeled spots, with the exception of lysine. This pattern could also be produced by strong inhibition of cytoplasmic protein synthesis with cycloheximide, and was abolished by preincubation with the mitochondrial protein synthesis inhibitor chloramphenicol. It appears therefore that the spots represent mitochondrial protein synthesis and that animal cells must have separate aminoacyl-tRNA synthetases for mitochondrial tRNAs corresponding to all these amino acids except, possibly, for lysine. The Rockefeller University Press 1984-04-01 /pmc/articles/PMC2113223/ /pubmed/6715412 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids
title Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids
title_full Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids
title_fullStr Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids
title_full_unstemmed Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids
title_short Selective synthesis of mitochondrial proteins by Chinese hamster ovary cells severely starved for various amino acids
title_sort selective synthesis of mitochondrial proteins by chinese hamster ovary cells severely starved for various amino acids
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113223/
https://www.ncbi.nlm.nih.gov/pubmed/6715412