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Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin

The quadriflagellate alga polytomella agilis contains several α-tubulins with distinct isoelectric points (McKeithan, T.W., and J.L. Rosenbaum, 1981, J. Cell Biol., 91:352-360). While α-3 is the major component in flagella, α-1 predominates in cytoskeletal microtubules. For determination of whether...

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Detalles Bibliográficos
Autores principales: McKeithan, TW, Lefebvre, PA, Silflow, CD, Rosenbaum, JL
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1983
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112316/
https://www.ncbi.nlm.nih.gov/pubmed/6833391
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author McKeithan, TW
Lefebvre, PA
Silflow, CD
Rosenbaum, JL
author_facet McKeithan, TW
Lefebvre, PA
Silflow, CD
Rosenbaum, JL
author_sort McKeithan, TW
collection PubMed
description The quadriflagellate alga polytomella agilis contains several α-tubulins with distinct isoelectric points (McKeithan, T.W., and J.L. Rosenbaum, 1981, J. Cell Biol., 91:352-360). While α-3 is the major component in flagella, α-1 predominates in cytoskeletal microtubules. For determination of whether the differences in α- tubulins are due to distinct genes or to posttranslational modification of a common α-tubulin precursor, poly A+ RNA was isolated from deflagellated and control (nonregenerating) cells and translated in vitro. Approximately twice as much α-1 was synthesized using RNA from deflagellated as compared to control cells; however, there was no detectable synthesis in vitro of α-3 in either. These results suggest that α -3 tubulin is formed in vivo by posttranslational modification of a form co- migrating with, and possibly identical to, cytoskeletal α-tubulin. In the related alga chlamydomonas reinhardii deflagellation greatly stimulates synthesis of tubulin and tubulin mRNA. As in polytomella, the principal α-tubulin synthesized both in vivo and in vitro following deflagellation in chlamydomonas is more basic than the major α-tubulin and appears to correspond to α-1 tubulin in polytomella. The conversion of α-1 to α-3 receives additional support from in vivo labeling and pulse-chase experiments. In addition, in both polytomella and chlamydomonas some conversion of α-1 to α-3 appears to occur even when protein synthesis is inhibited.
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spelling pubmed-21123162008-05-01 Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin McKeithan, TW Lefebvre, PA Silflow, CD Rosenbaum, JL J Cell Biol Articles The quadriflagellate alga polytomella agilis contains several α-tubulins with distinct isoelectric points (McKeithan, T.W., and J.L. Rosenbaum, 1981, J. Cell Biol., 91:352-360). While α-3 is the major component in flagella, α-1 predominates in cytoskeletal microtubules. For determination of whether the differences in α- tubulins are due to distinct genes or to posttranslational modification of a common α-tubulin precursor, poly A+ RNA was isolated from deflagellated and control (nonregenerating) cells and translated in vitro. Approximately twice as much α-1 was synthesized using RNA from deflagellated as compared to control cells; however, there was no detectable synthesis in vitro of α-3 in either. These results suggest that α -3 tubulin is formed in vivo by posttranslational modification of a form co- migrating with, and possibly identical to, cytoskeletal α-tubulin. In the related alga chlamydomonas reinhardii deflagellation greatly stimulates synthesis of tubulin and tubulin mRNA. As in polytomella, the principal α-tubulin synthesized both in vivo and in vitro following deflagellation in chlamydomonas is more basic than the major α-tubulin and appears to correspond to α-1 tubulin in polytomella. The conversion of α-1 to α-3 receives additional support from in vivo labeling and pulse-chase experiments. In addition, in both polytomella and chlamydomonas some conversion of α-1 to α-3 appears to occur even when protein synthesis is inhibited. The Rockefeller University Press 1983-04-01 /pmc/articles/PMC2112316/ /pubmed/6833391 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
McKeithan, TW
Lefebvre, PA
Silflow, CD
Rosenbaum, JL
Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
title Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
title_full Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
title_fullStr Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
title_full_unstemmed Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
title_short Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
title_sort multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112316/
https://www.ncbi.nlm.nih.gov/pubmed/6833391
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