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PMID: 3283651 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Four murine c-abl mRNAs arise by usage of two transcriptional promoters and alternative splicing.

Oncogene ·Vol. 2 ·No. 4 ·1988-04-00 ·Pages 297-304

Bernards A, Paskind M, Baltimore D

Abstract

The c-abl gene in mice is transcribed into two major and at least two minor mRNAs which have different 5'-ends, but are otherwise colinear. Here we show that the two major mRNAs are initiated by separate promoters and that the minor transcripts arise by alternative splicing. Like in the human gene, one of the alternative murine 5' c-abl exons lies far upstream of the remaining exons. The major mRNA that begins with this exon has about 1275 nucleotides upstream of the abl coding region. Interestingly, this unusually long upstream mRNA segment contains multiple short open reading frames both in mouse and man and is highly conserved in sequence between these species. The 5'-most c-abl promoter contains several sequence motifs that are highly conserved between mouse and man. The downstream promoter is much less conserved.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Humans Mice Molecular Sequence Data Promoter Regions, Genetic Proto-Oncogene Proteins/genetics Proto-Oncogene Proteins c-abl Proto-Oncogenes RNA Splicing RNA, Messenger/biosynthesis Sequence Homology, Nucleic Acid Transcription, Genetic
Chemicals
Proto-Oncogene Proteins RNA, Messenger Proto-Oncogene Proteins c-abl
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bernards A
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
Paskind M
Baltimore D
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1988-04-00
Pages
297-304
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · CA 38497 · United States
Databases
GENBANK
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