Null mutations in the lin-31 gene indicate two functions during Caenorhabditis elegans vulval development

Genetics. 2000 Dec;156(4):1595-602. doi: 10.1093/genetics/156.4.1595.

Abstract

The lin-31 gene is required for the proper specification of vulval cell fates in the nematode Caenorhabditis elegans and encodes a member of the winged-helix family of transcription factors. Members of this important family have been identified in many organisms and are known to bind specific DNA targets involved in a variety of developmental processes. DNA sequencing of 13 lin-31 alleles revealed six nonsense mutations and two missense mutations within the DNA-binding domain, plus three deletions, one transposon insertion, and one frameshift mutation that all cause large-scale disruptions in the gene. The missense mutations are amino acid substitutions in the DNA-binding domain and probably disrupt interactions of the LIN-31 transcription factor with its DNA target. In addition, detailed phenotypic analysis of all 19 alleles showed similar penetrance for several characteristics examined. From our analysis we conclude: (1) the null phenotype of lin-31 is the phenotype displayed by almost all of the existing alleles, (2) the DNA-binding domain plays a critical role in LIN-31 function, and (3) direct screens for multivulva and vulvaless mutants will probably yield only null (or strong) alleles of lin-31.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Amino Acid Substitution
  • Animals
  • Binding Sites
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans Proteins*
  • Codon, Nonsense
  • DNA Mutational Analysis
  • DNA, Helminth / genetics
  • DNA, Helminth / metabolism
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / physiology
  • Disorders of Sex Development
  • Female
  • Genes, Helminth*
  • Helminth Proteins / genetics*
  • Helminth Proteins / physiology
  • Male
  • Molecular Sequence Data
  • Morphogenesis
  • Multigene Family
  • Mutation, Missense
  • Phenotype
  • Protein Structure, Tertiary
  • Sequence Alignment
  • Sequence Deletion
  • Sequence Homology, Amino Acid
  • Transcription Factors / genetics*
  • Transcription Factors / physiology
  • Vulva / abnormalities
  • Vulva / cytology
  • Vulva / embryology*

Substances

  • Caenorhabditis elegans Proteins
  • Codon, Nonsense
  • DNA, Helminth
  • DNA-Binding Proteins
  • Helminth Proteins
  • Transcription Factors
  • lin-31 protein, C elegans