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Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors

Polyadenylated RNA from Chlamydomonas was translated in a cell-free rabbit reticulocyte system that employed [35S]methionine. Antibodies made to four chloroplast ribosomal proteins synthesized in the cytoplasm and imported into the organelle were used for indirect immunoprecipitation of the labeled...

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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/PMC2113070/
https://www.ncbi.nlm.nih.gov/pubmed/6202701
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description Polyadenylated RNA from Chlamydomonas was translated in a cell-free rabbit reticulocyte system that employed [35S]methionine. Antibodies made to four chloroplast ribosomal proteins synthesized in the cytoplasm and imported into the organelle were used for indirect immunoprecipitation of the labeled translation products, which were subsequently visualized on fluorographs of SDS gels. The cytoplasmically synthesized chloroplast ribosomal proteins were first seen as precursors with apparent molecular weights of 1,000 to 6,000 greater than their respective mature forms. Processing of the ribosomal protein precursors to mature proteins was affected by adding a postribosomal supernatant that had been extracted from cells of Chlamydomonas. In contrast to the chloroplast ribosomal proteins synthesized in the cytoplasm, two such proteins made within the chloroplast were found to be synthesized in mature form in cell-free wheat germ translation systems programmed with nonpolyadenylated RNA.
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spelling pubmed-21130702008-05-01 Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors J Cell Biol Articles Polyadenylated RNA from Chlamydomonas was translated in a cell-free rabbit reticulocyte system that employed [35S]methionine. Antibodies made to four chloroplast ribosomal proteins synthesized in the cytoplasm and imported into the organelle were used for indirect immunoprecipitation of the labeled translation products, which were subsequently visualized on fluorographs of SDS gels. The cytoplasmically synthesized chloroplast ribosomal proteins were first seen as precursors with apparent molecular weights of 1,000 to 6,000 greater than their respective mature forms. Processing of the ribosomal protein precursors to mature proteins was affected by adding a postribosomal supernatant that had been extracted from cells of Chlamydomonas. In contrast to the chloroplast ribosomal proteins synthesized in the cytoplasm, two such proteins made within the chloroplast were found to be synthesized in mature form in cell-free wheat germ translation systems programmed with nonpolyadenylated RNA. The Rockefeller University Press 1984-06-01 /pmc/articles/PMC2113070/ /pubmed/6202701 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
Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors
title Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors
title_full Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors
title_fullStr Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors
title_full_unstemmed Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors
title_short Chloroplast ribosomal proteins of Chlamydomonas synthesized in the cytoplasm are made as precursors
title_sort chloroplast ribosomal proteins of chlamydomonas synthesized in the cytoplasm are made as precursors
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113070/
https://www.ncbi.nlm.nih.gov/pubmed/6202701