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PMID: 1690869 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Structure of the complete human c-fgr proto-oncogene and identification of multiple transcriptional start sites.

Oncogene ·Vol. 5 ·No. 2 ·1990-02-00 ·Pages 201-6

Patel M, Leevers SJ, Brickell PM

Abstract

Here we report the isolation of cosmid clones containing the whole of the human c-fgr proto-oncogene. We have used these to determine the organization and nucleotide sequence of the exons upstream of exon 4, which have not previously been analysed. We show that, like exons 4 to 12, exon 3 closely resembles its counterpart in the avian c-src and murine lck genes. In contrast, the organization of the upstream exons of c-fgr differs markedly. In particular, the 5' untranslated regions of the c-fgr gene is interrupted by an extra intron. We have also mapped multiple transcriptional start sites within the 5' flanking region of the c-fgr gene and present an analysis of the nucleotide sequences within this region which may be responsible for regulating c-fgr expression.

MeSH Terms
Base Sequence Exons Humans Introns Protein-Tyrosine Kinases/genetics Proto-Oncogene Mas Proto-Oncogene Proteins/genetics Proto-Oncogene Proteins pp60(c-src) Proto-Oncogenes Transcription, Genetic src-Family Kinases
Chemicals
MAS1 protein, human Proto-Oncogene Mas Proto-Oncogene Proteins Protein-Tyrosine Kinases Proto-Oncogene Proteins pp60(c-src) proto-oncogene proteins c-fgr src-Family Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Patel M
Department of Biochemistry, University College of Middlesex School of Medicine, London, UK.
Leevers S J
Brickell P M
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1990-02-00
Pages
201-6
Language
English
Region
England
NLM ID
8711562
Subset
IM
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