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Distinct Isoforms of the RFX Transcription Factor DAF-19 Regulate Ciliogenesis and Maintenance of Synaptic Activity
Södertörn University, School of Life Sciences.
Södertörn University, School of Life Sciences.
2008 (English)In: Molecular Biology of the Cell, ISSN 1059-1524, E-ISSN 1939-4586, Vol. 19, no 12, 5517-5528 p.Article in journal (Refereed) Published
Abstract [en]

Neurons form elaborate subcellular structures such as dendrites, axons, cilia, and synapses to receive signals from their environment and to transmit them to the respective target cells. In the worm Caenorhabditis elegans, lack of the RFX transcription factor DAF-19 leads to the absence of cilia normally found on 60 sensory neurons. We now describe and functionally characterize three different isoforms of DAF-19. The short isoform DAF-19C is specifically expressed in ciliated sensory neurons and sufficient to rescue all cilia-related phenotypes of daf-19 mutants. In contrast, the long isoforms DAF-19A/B function in basically all nonciliated neurons. We discovered behavioral and cellular phenotypes in daf-19 mutants that depend on the isoforms daf-19a/b. These novel synaptic maintenance phenotypes are reminiscent of synaptic decline seen in many human neurodegenerative disorders. The C. elegans daf-19 mutant worms can thus serve as a molecular model for the mechanisms of functional neuronal decline.

Place, publisher, year, edition, pages
2008. Vol. 19, no 12, 5517-5528 p.
National Category
Cell Biology
Identifiers
URN: urn:nbn:se:sh:diva-14115DOI: 10.1091/mbc.E08-04-0416ISI: 000261244700041OAI: oai:DiVA.org:sh-14115DiVA: diva2:467051
Available from: 2011-12-18 Created: 2011-12-16 Last updated: 2011-12-18Bibliographically approved

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Senti, GabrieleSwoboda, Peter
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