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Gene Review

lin-32  -  Protein LIN-32

Caenorhabditis elegans

 
 
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High impact information on lin-32

  • Mutations in hlh-2, the gene encoding the C. elegans E/daughterless ortholog, enhance the ray defects caused by lin-32 mutations [1].
  • Previous studies have identified three genes (lin-32, unc-86 and mec-3) that regulate touch cell development [2].
  • A similar touch cell phenotype is produced by mutations in lin-32 [3].
  • Here we show that MAB-3 promotes expression of the proneural protein LIN-32 in V ray precursors by transcriptional repression of ref-1, a member of the Hes family of neurogenic factors [4].
 

Other interactions of lin-32

  • The atonal ortholog lin-32 and the E/daughterless ortholog hlh-2 act to confer neural competence during ray development, but additional regulatory factors that control specific aspects of cell fate are largely unknown [5].

References

 
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