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  • Open Access

A screen for mutants with abnormal cilia number in C. elegans

Cilia20121 (Suppl 1) :P61

https://doi.org/10.1186/2046-2530-1-S1-P61

  • Published:

Keywords

  • Molecular Mechanism
  • Early Phase
  • Developmental Biology
  • Molecular Basis
  • Cell Fate

To date, while molecular basis of intraflagellar transport (IFT) has been well studied, little is known about the mechanisms underlying the early phase of ciliogenesis. In Caenorhabditis elegans, sensory neurons are associated with one or two cilia. The number is not stochastically but strictly determined according to the cell fate. For example, one of the head sensory neuron class, ADL, is double ciliated, whereas another sensory neuron class, ASE, is single ciliated. To dissect molecular mechanisms that determine the number of cilia, we screen for mutants with abnormal cilia number. Through the screening, we obtained three mutants, in which ADL is single ciliated. In these mutants, ADL cilium did not display short-length phenotype, which is typically observed in IFT-defective mutants. Currently, we are mapping the mutations responsible for the abnormal cilia number phenotype.

Authors’ Affiliations

(1)
Kanagawa University, Japan

Copyright

© Adachi; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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