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LET-23 Receptor Localization by the Cell Junction Protein LIN-7 during C. elegans Vulval Induction

Open access
Simske, Jeffrey S, Kaech, Susan M, Harp, Stacey A, Kim, Stuart K·1996·Cell

Abstract

In C. elegans, the anchor cell signal induces Pn.p cells to form the vulva by activating a conserved receptor tyrosine kinase pathway. lin-2 and lin-7 mutants exhibit a vulvaless phenotype similar to the phenotype observed when this signaling pathway is defective. We have found that LIN-7 is a cell junction-associated protein that binds to the LET-23 receptor tyrosine kinase. LET-23 is also localized to the cell junctions, and both LIN-2 and LIN-7 are required for this localization. LET-23 overexpression rescues the lin-2 or lin-7 vulvaless phenotype, suggesting that increased receptor density can compensate for mislocalization. These results suggest that proper localization of LET-23 receptor to the Pn.p cell junctions is required for signaling activity.

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Metadata

Authors
Simske, J. S., Kaech, S. M., Harp, S. A., & Kim, S. K.
Venue
Cell
Publisher
Elsevier BV
Published
1996-04
Volume
85
Issue
2
Pages
195-204
ISSN
0092-8674 (ISSN-L)
OpenAlex
W2104008077
Cited by
265
References
0
FWCI
11.13
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: LET-23 Receptor Localization by the Cell Junction Protein LIN-7 during C. elegans Vulval Induction. https://app.cochat.ai/papers/10.1016/s0092-8674(00)81096-x
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Simske, J. S., Kaech, S. M., Harp, S. A., & Kim, S. K. (1996). LET-23 Receptor Localization by the Cell Junction Protein LIN-7 during C. elegans Vulval Induction. Cell. https://doi.org/10.1016/s0092-8674(00)81096-x

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.