Literature DB >> 12445822

Alternative splicing variants of the human DBL (MCF-2) proto-oncogene.

Koichiro Komai1, Rie Okayama, Michinori Kitagawa, Hirofumi Yagi, Kazuo Chihara, Shunichi Shiozawa.   

Abstract

The DBL (MCF-2) proto-oncogene is a prototype guanine nucleotide exchange factor (GEF) that modulates the Rho family of GTPases. In this communication we describe the isolation of three novel splicing variants of Dbl. The prototype Dbl gene (designated var.1 here) contains 25 exons, while splicing variant 2 (var.2) lacks exons 23 and 24. Var.3 contains additional 3 exons from 5(')-UTR in place of exon 1, while var.4, var.2, and var.3 contain a 48bp insertion between exons 10 and 11, resulting in the insertion of 16 amino acids. We found that var.1 was expressed only in brain, whereas var.3 was expressed in heart, kidney, spleen, liver, and testis, and var.4 in brain, heart, kidney, testis, placenta, stomach, and peripheral blood. The Dbl protein was detectable in brain, heart, kidney, intestine, muscle, lung, and testis. An assay for GEF activity revealed that the var.2 exhibits decreased GEF activity towards Cdc42, var.3 exhibits a weak but significant activity toward Rac1 and Cdc42, var.4 exhibits significant activity toward RhoA and Cdc42, while var.1 exhibits no activity toward RhoA, Rac1, or Cdc42. In summary, we describe 4 splicing variants of the human DBL proto-oncogene that show different tissue distributions and GEF specificities.

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Year:  2002        PMID: 12445822     DOI: 10.1016/s0006-291x(02)02645-1

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  High frequency of development of B cell lymphoproliferation and diffuse large B cell lymphoma in Dbl knock-in mice.

Authors:  Marzia Ognibene; Ottavia Barbieri; Cristina Vanni; Luca Mastracci; Simonetta Astigiano; Laura Emionite; Barbara Salani; Manuela Fedele; Roberta Resaz; Claudya Tenca; Franco Fais; Federica Sabatini; Amleto De Santanna; Fiorella Altruda; Luigi Varesio; Emilio Hirsch; Alessandra Eva
Journal:  J Mol Med (Berl)       Date:  2011-01-11       Impact factor: 4.599

2.  A fourteen gene GBM prognostic signature identifies association of immune response pathway and mesenchymal subtype with high risk group.

Authors:  Arivazhagan Arimappamagan; Kumaravel Somasundaram; Kandavel Thennarasu; Sreekanthreddy Peddagangannagari; Harish Srinivasan; Bangalore C Shailaja; Cini Samuel; Irene Rosita Pia Patric; Sudhanshu Shukla; Balaram Thota; Krishnarao Venkatesh Prasanna; Paritosh Pandey; Anandh Balasubramaniam; Vani Santosh; Bangalore Ashwathnarayanara Chandramouli; Alangar Sathyaranjandas Hegde; Paturu Kondaiah; Manchanahalli R Sathyanarayana Rao
Journal:  PLoS One       Date:  2013-04-30       Impact factor: 3.240

3.  Epithelial junction formation requires confinement of Cdc42 activity by a novel SH3BP1 complex.

Authors:  Ahmed Elbediwy; Ceniz Zihni; Stephen J Terry; Peter Clark; Karl Matter; Maria S Balda
Journal:  J Cell Biol       Date:  2012-08-13       Impact factor: 10.539

4.  Dbl3 drives Cdc42 signaling at the apical margin to regulate junction position and apical differentiation.

Authors:  Ceniz Zihni; Peter M G Munro; Ahmed Elbediwy; Nicholas H Keep; Stephen J Terry; John Harris; Maria S Balda; Karl Matter
Journal:  J Cell Biol       Date:  2013-12-30       Impact factor: 10.539

  4 in total

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