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Identification and Characterization of a Novel Allele of Caenorhabditis elegans bbs-7
Author(s) -
Kara M. Braunreiter,
Shelby Hamlin,
Jamie LymanGingerich
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0113737
Subject(s) - cilium , caenorhabditis elegans , biology , intraflagellar transport , microbiology and biotechnology , motile cilium , mutant , genetic screen , genetics , mutation , missense mutation , mechanosensation , gene , receptor , ion channel
Primary cilia play a role in the sensation of and response to the surrounding environment. Caenorhabditis elegans (C. elegans) have primary cilia only on the distal tips of some dendrites. In order to better understand the relationship between receptor localization to cilia, cilia structure and cilia function, we have characterized a mutation originally identified in a forward genetic screen for mutants with defective PKD-2 ciliary localization. Through behavioral assays and examination of the structure of cilia in the cil-5 ( my13) mutant animals, we have found that my13 disrupts not only receptor localization, but also some cilia-mediated sensory behaviors and cilia structural integrity. We have identified the my13 lesion and found that it is a missense mutation in bbs-7 , an ortholog of human BBS-7, a gene known to affect human cilia and to be involved in Bardet-Biedl syndrome. Finally, we show that bbs-7(my13) also affects the glia cells which support the cilia.

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