Cadherin–catenin complexes, localized to adherens junctions, are essential for cell–cell adhesion. One means of regulating adhesion is through the juxtamembrane domain of the cadherin cytoplasmic tail. This region is the binding site for p120, leading to the hypothesis that p120 is a key regulator of cell adhesion. p120 has also been suggested to regulate the GTPase Rho and to regulate transcription via its binding partner Kaiso. To test these hypothesized functions, we turned to Drosophila, which has only a single p120 family member. It localizes to adherens junctions and binds the juxtamembrane region of DE-cadherin (DE-cad). We generated null alleles of p120 and found that mutants are viable and fertile and have no substantial changes in junction structure or function. However, p120 mutations strongly enhance mutations in the genes encoding DE-cadherin or Armadillo, the β-catenin homologue. Finally, we examined the localization of p120 during embryogenesis. p120 localizes to adherens junctions, but its localization there is less universal than that of core adherens junction proteins. Together, these data suggest that p120 is an important positive modulator of adhesion but that it is not an essential core component of adherens junctions.
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3 February 2003
Article|
January 27 2003
Drosophila p120catenin plays a supporting role in cell adhesion but is not an essential adherens junction component
Steven H. Myster,
Steven H. Myster
1Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Robert Cavallo,
Robert Cavallo
2Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Charles T. Anderson,
Charles T. Anderson
3Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Donald T. Fox,
Donald T. Fox
3Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Mark Peifer
Mark Peifer
1Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
2Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
3Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Steven H. Myster
1Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Robert Cavallo
2Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Charles T. Anderson
3Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Donald T. Fox
3Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Mark Peifer
1Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
2Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
3Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Address correspondence to Mark Peifer, Dept. of Biology, CB#3280, Coker Hall, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280. Tel.: (919) 962-2271. Fax: (919) 962-1625. E-mail: [email protected]
*
Abbreviations used in this paper: AJ, adherens junction; Arm, Armadillo; BDGP, Berkeley Drosophila Genome Project; α-cat, α-catenin; β-cat, β-catenin; CNS, central nervous system; DE-cad, DE-cadherin, shg, shotgun; IP, immunoprecipitate; JM, juxtamembrane; RNAi, RNA interference; Wg, Wingless.
Received:
November 19 2002
Revision Received:
December 23 2002
Accepted:
December 23 2002
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 160 (3): 433–449.
Article history
Received:
November 19 2002
Revision Received:
December 23 2002
Accepted:
December 23 2002
Citation
Steven H. Myster, Robert Cavallo, Charles T. Anderson, Donald T. Fox, Mark Peifer; Drosophila p120catenin plays a supporting role in cell adhesion but is not an essential adherens junction component . J Cell Biol 3 February 2003; 160 (3): 433–449. doi: https://doi.org/10.1083/jcb.200211083
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