Cited by 203Developmental Biology and Gene RegulationProtein Kinase Regulation and GTPase SignalingCell Adhesion Molecules Research

The C. elegans vulval induction gene lin-2 encodes a member of the MAGUK family of cell junction proteins

Hoskins, Roger, Hajnal, Alex F., Harp, Stacey A., Kim, Stuart K.·1996·Development

Abstract

The lin-2 gene is required for the induction of the Caenorhabditis elegans vulva. Vulval development is initiated by a signal from the anchor cell that is transduced by a receptor tyrosine kinase/Ras pathway. We show that lin-2 acts in the vulval precursor cell P6.p, downstream of lin-3 EGF and upstream of let-60 ras, to allow expression of the 1 degrees cell fate. lin-2 encodes a protein of relative molecular mass 109,000 (LIN-2A) with regions of similarity to CaM kinase II and membrane-associated guanylate kinases. Mutant lin-2 transgenes designed to lack either protein kinase or guanylate kinase activity are functional, indicating that LIN-2A has a structural rather than an enzymatic role in vulval induction. Most or all identified membrane-associated guanylate kinases are components of cell junctions, including vertebrate tight junctions and arthropod septate junctions in epithelia. Thus, LIN-2A may be a component of the cell junctions of the epithelial vulval precursor cells that is required for signaling by the receptor tyrosine kinase LET-23. We propose that LIN-2A is required for the localization of one or more signal transduction proteins (such as LET-23) to either the basal membrane domain or the cell junctions, and that mislocalization of signal transduction proteins in lin-2 mutants interferes with vulval induction.

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Crossref · 10.1242/dev.122.1.97

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  • Mutations of CASK produce a developmental phenotype in invertebrates, mice, and humans and cause major changes in neuronal function, including a general impairment of synaptic transmission.

    “Mutations of CASK produce a developmental phenotype in invertebrates, mice, and humans (Hoskins et al., 1996; Atasoy et al., 2007; Moog et al., 2011) and cause major changes in neuronal function, including a general impairment of synaptic transmission (Zordan et al., 2005; Atasoy et al., 2007; Sun et al., 2009; Chen and Featherstone, 2011).”

    From The Presynaptic Active Zone (2012) · cites this paper as Hoskins et al., 1996

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References 78 · Cited by 203

Authors
Hoskins, R., Hajnal, A. F., Harp, S. A., & Kim, S. K.
Affiliations
Stanford Medicine (US)
Venue
Development
Published
1996-01-01
Volume
122
Issue
1
Pages
97-111
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2103093241
Cited by
203
References
78
Citations by year
2026: 2 · 2025: 1 · 2024: 1 · 2022: 2 · 2020: 5 · 2019: 3 · 2018: 3 · 2017: 3 · 2016: 3 · 2015: 2 · 2014: 1 · 2013: 4 · 2012: 8
FWCI
10.22
Type
journal article
Language
en
Open access
closed
Locations
  • Development (publishedVersion)
  • PubMed (publishedVersion)
  • HighWire Press Open Archive (submittedVersion)
  • PubMed
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
Keywords
vulval induction, Caenorhabditis elegans, cell junctions, receptor tyrosine kinase, LET-23, vulval precursor cells, protein kinase activity, signal transduction, epithelial cell junctions, tight junctions, septate junctions
MeSH terms
Amino Acid Sequence, Animals, Base Sequence, Cloning, Molecular, Female, Intercellular Junctions, Membrane Proteins, Molecular Sequence Data, Genes, ras, RNA, Messenger, Stem Cells, Vulva, Signal Transduction, Helminth Proteins, Caenorhabditis elegans, Genes, Helminth, Sequence Homology, Amino Acid, DNA Primers, DNA, Helminth, Caenorhabditis elegans Proteins, ErbB Receptors

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