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Proteomic Analysis Reveals CACN-1 Is a Component of the Spliceosome inCaenorhabditis elegans
Author(s) -
Michael F. Doherty,
Guillaume Adelmant,
Alyssa D. Cecchetelli,
Jarrod A. Marto,
Erin J. Cram
Publication year - 2014
Publication title -
g3 genes genomes genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.468
H-Index - 66
ISSN - 2160-1836
DOI - 10.1534/g3.114.012013
Subject(s) - caenorhabditis elegans , biology , spliceosome , rna interference , tandem affinity purification , model organism , proteomics , microbiology and biotechnology , gene , genetic screen , rna splicing , genetics , phenotype , wnt signaling pathway , proteome , alternative splicing , computational biology , rna , messenger rna , biochemistry , affinity chromatography , enzyme
Cell migration is essential for embryonic development and tissue formation in all animals. cacn-1 is a conserved gene of unknown molecular function identified in a genome-wide screen for genes that regulate distal tip cell migration in the nematode worm Caenorhabditis elegans. In this study we take a proteomics approach to understand CACN-1 function. To isolate CACN-1-interacting proteins, we used an in vivo tandem-affinity purification strategy. Tandem-affinity purification-tagged CACN-1 complexes were isolated from C. elegans lysate, analyzed by mass spectrometry, and characterized bioinformatically. Results suggest significant interaction of CACN-1 with the C. elegans spliceosome. All of the identified interactors were screened for distal tip cell migration phenotypes using RNAi. Depletion of many of these factors led to distal tip cell migration defects, particularly a failure to stop migrating, a phenotype commonly seen in cacn-1 deficient animals. The results of this screen identify eight novel regulators of cell migration and suggest CACN-1 may participate in a protein network dedicated to high-fidelity gonad development. The composition of proteins comprising the CACN-1 network suggests that this critical developmental module may exert its influence through alternative splicing or other post-transcriptional gene regulation.

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