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Multiple forms of tubulin in polytomella and chlamydomonas: evidence for a precursor of flagellar α-tubulin
- Source :
- The Journal of Cell Biology
- Publication Year :
- 1983
- Publisher :
- Rockefeller University Press, 1983.
-
Abstract
- The quadriflagellate alga polytomella agilis contains several alpha-tubulins with distinct isoelectric points (McKeithan, T.W., and J.L. Rosenbaum, 1981, J. Cell Biol., 91:352-360). While alpha-3 is the major component in flagella, alpha-1 predominates in cytoskeletal microtubules. For determination of whether the differences in alpha- tubulins are due to distinct genes or to posttranslational modification of a common alpha-tubulin precursor, poly A+ RNA was isolated from deflagellated and control (nonregenerating) cells and translated in vitro. Approximately twice as much alpha-1 was synthesized using RNA from deflagellated as compared to control cells; however, there was no detectable synthesis in vitro of alpha-3 in either. These results suggest that alpha -3 tubulin is formed in vivo by posttranslational modification of a form co- migrating with, and possibly identical to, cytoskeletal alpha-tubulin. In the related alga chlamydomonas reinhardii deflagellation greatly stimulates synthesis of tubulin and tubulin mRNA. As in polytomella, the principal alpha-tubulin synthesized both in vivo and in vitro following deflagellation in chlamydomonas is more basic than the major alpha-tubulin and appears to correspond to alpha-1 tubulin in polytomella. The conversion of alpha-1 to alpha-3 receives additional support from in vivo labeling and pulse-chase experiments. In addition, in both polytomella and chlamydomonas some conversion of alpha-1 to alpha-3 appears to occur even when protein synthesis is inhibited.
- Subjects :
- Messenger RNA
biology
Chlamydomonas
Polytomella
Eukaryota
RNA
Articles
macromolecular substances
Cell Biology
biology.organism_classification
Microtubules
Cell biology
Tubulin
Flagella
Microtubule
Protein Biosynthesis
biology.protein
Protein biosynthesis
Protein Precursors
Cytoskeleton
Protein Processing, Post-Translational
Subjects
Details
- ISSN :
- 15408140 and 00219525
- Volume :
- 96
- Database :
- OpenAIRE
- Journal :
- Journal of Cell Biology
- Accession number :
- edsair.doi.dedup.....ed8d209c95a80ab18f520c084ba35c0a
- Full Text :
- https://doi.org/10.1083/jcb.96.4.1056