We describe here the molecular and functional characterization of the Caenorhabditis elegans unc-97 gene, whose gene product constitutes a novel component of muscular adherens junctions. UNC-97 and homologues from several other species define the PINCH family, a family of LIM proteins whose modular composition of five LIM domains implicates them as potential adapter molecules. unc-97 expression is restricted to tissue types that attach to the hypodermis, specifically body wall muscles, vulval muscles, and mechanosensory neurons. In body wall muscles, the UNC-97 protein colocalizes with the β-integrin PAT-3 to the focal adhesion-like attachment sites of muscles. Partial and complete loss-of-function studies demonstrate that UNC-97 affects the structural integrity of the integrin containing muscle adherens junctions and contributes to the mechanosensory functions of touch neurons. The expression of a Drosophila homologue of unc-97 in two integrin containing cell types, muscles, and muscle-attached epidermal cells, suggests that unc-97 function in adherens junction assembly and stability has been conserved across phylogeny. In addition to its localization to adherens junctions UNC-97 can also be detected in the nucleus, suggesting multiple functions for this LIM domain protein.
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11 January 1999
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January 11 1999
A Conserved LIM Protein That Affects Muscular Adherens Junction Integrity and Mechanosensory Function in Caenorhabditis elegans
Oliver Hobert,
Oliver Hobert
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
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Donald G. Moerman,
Donald G. Moerman
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
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Kathleen A. Clark,
Kathleen A. Clark
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
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Mary C. Beckerle,
Mary C. Beckerle
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
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Gary Ruvkun
Gary Ruvkun
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
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Oliver Hobert
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
Donald G. Moerman
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
Kathleen A. Clark
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
Mary C. Beckerle
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
Gary Ruvkun
*Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114; ‡Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4; and §Department of Biology, University of Utah, Salt Lake City, Utah 84112
Address correspondence to O. Hobert, Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston, MA 02114. Tel.: (617) 726-5973. Fax: (617) 726-6893. E-mail: [email protected]
Received:
August 25 1998
Revision Received:
October 27 1998
Online ISSN: 1540-8140
Print ISSN: 0021-9525
1999
J Cell Biol (1999) 144 (1): 45–57.
Article history
Received:
August 25 1998
Revision Received:
October 27 1998
Citation
Oliver Hobert, Donald G. Moerman, Kathleen A. Clark, Mary C. Beckerle, Gary Ruvkun; A Conserved LIM Protein That Affects Muscular Adherens Junction Integrity and Mechanosensory Function in Caenorhabditis elegans . J Cell Biol 11 January 1999; 144 (1): 45–57. doi: https://doi.org/10.1083/jcb.144.1.45
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