Reference Report
| Reference | |||
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| Citation | Rudolf, A., Buttgereit, D., Rexer, K.H., Renkawitz-Pohl, R. (2012). The syncytial visceral and somatic musculature develops independently of β3-Tubulin during Drosophila embryogenesis, while maternally supplied β1-Tubulin is stable until the early steps of myoblast fusion. Europ. J. Cell Biol. 91(3): 192--203. (Export to RIS) | ||
| FlyBase ID | FBrf0217503 | ||
| Publication Type | Research paper | ||
| PubMed ID | 22306378 | ||
| PubMed Abstract | Microtubules are necessary for fusion and elongation of vertebrate muscle cells. In Drosophila, several isoforms of β-Tubulin, the functional subunit of microtubules, are expressed in different tissues of the developing embryo, while solely the β3-Tubulin isoform is detected in large amounts during differentiation of the somatic and visceral musculature. Here we show the unexpected result that all mesodermal tissues develop correctly in β3-Tubulin loss of function mutants. Furthermore, we show that β2-Tubulin transcripts are not detectable in embryos and an exceptional zygotic β1-Tubulin expression in β3-Tubulin mutants cannot be observed. Nevertheless, a maternally contributed β1-Tubulin-GFP fusion protein (from protein trap collection, Buszczak et al., 2007, Genetics 175, 1505-1531) acts in a dominant negative way, disturbing embryonic development from early stages on. This effect can be observed to the same extent in a zygotic β3-Tubulin mutant situation. Our results indicate that the maternally supplied β1-Tubulin based microtubule network is sufficient for myoblast fusion, myotube elongation and sarcomere formation both during visceral and somatic muscle development in Drosophila embryogenesis. | ||
| DOI | 10.1016/j.ejcb.2011.11.002 | ||
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| Language of Publication | English | ||
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| Publication Type | Journal | ||
| Abbreviation | Europ. J. Cell Biol. | ||
| Title | European Journal of Cell Biology | ||
| Publication Year | 1979- | ||
| ISBN/ISSN | 0171-9335 | ||
Data from Reference
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Aberrations (2)
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Alleles (7)
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Constructs (2)
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Genes (12)
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Insertions (3)
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Natural transposons (1)
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