Literature DB >> 11455956

Structure characterization of human RalGDS gene, and the identification of its novel variant.

Q Zheng1, L Yu, Y Zhao, H Zhang, Q Fu, N Mao, P Hu, Z Geng, S Zhao.   

Abstract

RalGDS is a guanine nucleotide dissociation stimulator for Ral, which is a member of the Ras GTPase superfamily that regulates cellular proliferation, differentiation and transformation by mediating multiple signal transduction pathways. RalGDS can specifically promote the conversion from an inactive GDP-bound state to an active GTP-bound state for Ral. The cDNA of human RalGDS has been cloned recently. In this paper, by comparison between the gene's genomic and cDNA seqence, we determined the structure of the gene, which showed that the reported human RalGDS transcribed from 18 exons. Furthermore, a novel variant of RalGDS that codes for a protein with a different N-terminus was cloned and identified. Northern hybridization revealed that the novel transcript was of 6.0 kb in length while the transcript previously reported is of 4.0 kb. Both transcripts were ubiquitously expressed in human adult tissues examined, albeit with different amounts. In addition, this novel transcript was proved to be caused by employment of a new exon, designated as exon 1a, instead of the one, designated as exon 1b, in the reported cDNA. Thus, the RalGDS gene consists of at least 19 exons and spanned a 44 kb region. The length between exon 1a and exon 2 was 33 kb, while the length between exon 1b and exon 2 was 8.8 kb.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11455956     DOI: 10.1023/a:1011043122220

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  16 in total

1.  The TC21 oncoprotein interacts with the Ral guanosine nucleotide dissociation factor.

Authors:  M López-Barahona; X R Bustelo; M Barbacid
Journal:  Oncogene       Date:  1996-02-01       Impact factor: 9.867

2.  RalGDS-like factor (Rlf) is a novel Ras and Rap 1A-associating protein.

Authors:  R M Wolthuis; B Bauer; L J van 't Veer; A M de Vries-Smits; R H Cool; M Spaargaren; A Wittinghofer; B M Burgering; J L Bos
Journal:  Oncogene       Date:  1996-07-18       Impact factor: 9.867

3.  Identification of a novel RalGDS-related protein as a candidate effector for Ras and Rap1.

Authors:  S N Peterson; L Trabalzini; T R Brtva; T Fischer; D L Altschuler; P Martelli; E G Lapetina; C J Der; G C White
Journal:  J Biol Chem       Date:  1996-11-22       Impact factor: 5.157

Review 4.  ras genes.

Authors:  M Barbacid
Journal:  Annu Rev Biochem       Date:  1987       Impact factor: 23.643

5.  Double-mutant analysis of the interaction of Ras with the Ras-binding domain of RGL.

Authors:  M Shirouzu; K Hashimoto; A Kikuchi; S Yokoyama
Journal:  Biochemistry       Date:  1999-04-20       Impact factor: 3.162

Review 6.  Function and regulation of ras.

Authors:  D R Lowy; B M Willumsen
Journal:  Annu Rev Biochem       Date:  1993       Impact factor: 23.643

7.  Activated Ras interacts with the Ral guanine nucleotide dissociation stimulator.

Authors:  F Hofer; S Fields; C Schneider; G S Martin
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-08       Impact factor: 11.205

8.  Identification of the guanine nucleotide dissociation stimulator for Ral as a putative effector molecule of R-ras, H-ras, K-ras, and Rap.

Authors:  M Spaargaren; J R Bischoff
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

9.  Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1.

Authors:  D Humphrey; J Kwiatkowska; E P Henske; J L Haines; D Halley; M van Slegtenhorst; D J Kwiatkowski
Journal:  Ann Hum Genet       Date:  1997-07       Impact factor: 1.670

10.  ralGDS family members interact with the effector loop of ras p21.

Authors:  A Kikuchi; S D Demo; Z H Ye; Y W Chen; L T Williams
Journal:  Mol Cell Biol       Date:  1994-11       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.