Literature DB >> 17185752

Truncated isoform of mouse alphaT-catenin is testis-restricted in expression and function.

Steven Goossens1, Barbara Janssens, Griet Vanpoucke, Riet De Rycke, Jolanda van Hengel, Frans van Roy.   

Abstract

AlphaT-catenin is a recently identified member of the alpha-catenin family of cell-cell adhesion molecules. For decades it was thought that alpha-catenins mediate solid cell-cell adhesion by linking the cadherin-mediated cell-cell adhesion complex with the actin cytoskeleton. However, the roles of alpha-catenins in this classical adhesion model have been questioned recently. AlphaT-catenin has a restricted expression pattern, in contrast to the ubiquitously expressed alphaE-catenin. High levels of alphaT-catenin were detected in heart and testis. Northern and Western blot experiments indicated that besides the standard full-length alphaT-catenin transcript, smaller alternative transcripts are expressed in testis. We report the cloning of two alternative transcripts of the mouse alphaT-catenin gene (transcript-B and -X), both of which are expressed in a testis-restricted manner from two putative alternative promoters. Alternative transcript-X encodes a smaller protein, isoform-X, which lacks the amino-terminal beta-catenin binding domain of the standard mouse alphaT-catenin protein, and is therefore unable to restore cell-cell adhesion in an alpha-catenin-negative colon carcinoma cell line. Immunohistochemical analysis showed specific localization of the alphaT-catenin isoform-X in the differentiating germ cells. In contrast to the standard full-length alphaT-catenin protein, this shortened isoform-X can bind to l-afadin, an important component of the nectin/afadin/ponsin adhesion complex that reportedly is essential for spermatogenesis.

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Year:  2006        PMID: 17185752     DOI: 10.1096/fj.06-6066com

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  11 in total

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Authors:  Ilona A Kopera; Barbara Bilinska; C Yan Cheng; Dolores D Mruk
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2.  A novel FADS1 isoform potentiates FADS2-mediated production of eicosanoid precursor fatty acids.

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Journal:  J Lipid Res       Date:  2012-05-22       Impact factor: 5.922

Review 3.  Anchoring junctions as drug targets: role in contraceptive development.

Authors:  Dolores D Mruk; Bruno Silvestrini; C Yan Cheng
Journal:  Pharmacol Rev       Date:  2008-05-15       Impact factor: 25.468

4.  Heritable, Allele-Specific Chromosomal Looping between Tandem Promoters Specifies Promoter Usage of SHC1.

Authors:  Xichuan Li; Zhenzhen Lin; Hao Wang; Dan Zhao; Xing Xu; Yiliang Wei; Xiaoting Li; Xiaobo Li; Yougui Xiang; Lance S Terada; Zhe Liu
Journal:  Mol Cell Biol       Date:  2018-04-16       Impact factor: 4.272

Review 5.  Alpha T-catenin (CTNNA3): a gene in the hand is worth two in the nest.

Authors:  James D Smith; Maria H Meehan; John Crean; Amanda McCann
Journal:  Cell Mol Life Sci       Date:  2011-05-20       Impact factor: 9.261

Review 6.  New functions for alpha-catenins in health and disease: from cancer to heart regeneration.

Authors:  Alexia Vite; Jifen Li; Glenn L Radice
Journal:  Cell Tissue Res       Date:  2015-02-12       Impact factor: 5.249

7.  SPATA33 affects the formation of cell adhesion complex by interacting with CTNNA3 in TM4 cells.

Authors:  Ying Zhang
Journal:  Cell Tissue Res       Date:  2022-05-10       Impact factor: 5.249

8.  SEASTAR: systematic evaluation of alternative transcription start sites in RNA.

Authors:  Zhiyi Qin; Peter Stoilov; Xuegong Zhang; Yi Xing
Journal:  Nucleic Acids Res       Date:  2018-05-04       Impact factor: 16.971

9.  The evolutionary history of the catenin gene family during metazoan evolution.

Authors:  Zi-Ming Zhao; Albert B Reynolds; Eric A Gaucher
Journal:  BMC Evol Biol       Date:  2011-07-08       Impact factor: 3.260

10.  The effect of heterogeneous Transcription Start Sites (TSS) on the translatome: implications for the mammalian cellular phenotype.

Authors:  Francois-Xavier Dieudonné; Patrick B F O'Connor; Pascale Gubler-Jaquier; Haleh Yasrebi; Beatrice Conne; Sergey Nikolaev; Stylianos Antonarakis; Pavel V Baranov; Joseph Curran
Journal:  BMC Genomics       Date:  2015-11-21       Impact factor: 3.969

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