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Multiple Isoforms of Beta-TrCP Display Differential Activities in the Regulation of Wnt Signaling

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Journal Cell Signal
Date 2008 Oct 22
PMID 18929646
Citations 15
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Abstract

The F-box proteins beta-TrCP1 and 2 (beta-transducin repeat containing protein) have 2 and 3 isoforms, respectively, due to alternative splicing of exons encoding the N-terminal region. We identified an extra exon in between the previously known exons 1 and 2 of beta-TrCP1 and beta-TrCP2. Interestingly, sequence analysis suggested that many more isoforms are produced than previously identified, via the alternative splicing of all possible combination of exons II to V of beta-TrCP1 and exons II to IV of beta-TrCP2. Different mouse tissues show specific expression patterns of the isoforms, and the level of expression of the isoform that has been used in most published papers was very low. Yeast two-hybrid assays show that beta-TrCP1 isoforms containing exon III, which are the most highly expressed isoforms in most tissues, do not interact with Skp1. Indirect immunofluorescence analysis of transiently expressed beta-TrCP1 isoforms suggests that the presence of exon III causes beta-TrCP1 to localize in nuclei. Consistent with the above findings, isoforms including exon III showed a reduced ability to block ectopic embryonic axes induced via injection of Wnt8 or beta-catenin in Xenopus embryos. Overall, our data suggest that isoforms of beta-TrCPs generated by alternative splicing may have different biological roles.

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References
1.
Caceres J, Kornblihtt A . Alternative splicing: multiple control mechanisms and involvement in human disease. Trends Genet. 2002; 18(4):186-93. DOI: 10.1016/s0168-9525(01)02626-9. View

2.
Spiegelman V, Slaga T, Pagano M, Minamoto T, Ronai Z, Fuchs S . Wnt/beta-catenin signaling induces the expression and activity of betaTrCP ubiquitin ligase receptor. Mol Cell. 2000; 5(5):877-82. DOI: 10.1016/s1097-2765(00)80327-5. View

3.
Margottin-Goguet F, Hsu J, Loktev A, Hsieh H, Reimann J, Jackson P . Prophase destruction of Emi1 by the SCF(betaTrCP/Slimb) ubiquitin ligase activates the anaphase promoting complex to allow progression beyond prometaphase. Dev Cell. 2003; 4(6):813-26. DOI: 10.1016/s1534-5807(03)00153-9. View

4.
Fuchs S, Spiegelman V, Kumar K . The many faces of beta-TrCP E3 ubiquitin ligases: reflections in the magic mirror of cancer. Oncogene. 2004; 23(11):2028-36. DOI: 10.1038/sj.onc.1207389. View

5.
Lassot I, Segeral E, Berlioz-Torrent C, Durand H, Groussin L, Hai T . ATF4 degradation relies on a phosphorylation-dependent interaction with the SCF(betaTrCP) ubiquitin ligase. Mol Cell Biol. 2001; 21(6):2192-202. PMC: 86853. DOI: 10.1128/MCB.21.6.2192-2202.2001. View