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PMID: 3512096 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Alternative 5' exons in c-abl mRNA.

Cell ·Vol. 44 ·No. 4 ·1986-02-28 ·Pages 577-86

Ben-Neriah Y, Bernards A, Paskind M, Daley GQ, Baltimore D

Abstract

The cellular abl proto-oncogene encodes a protein-tyrosine kinase and is expressed in many cell types in two or three mRNA size species. Four types of mouse c-abl cDNAs have been cloned from 70Z/3 lymphoid cells that have different 5' sequences encoding predicted N-terminal regions of 20-45 amino acids. One of the four cDNAs has a predicted N-terminal sequence of met-gly-gln in common with the gag N terminus of v-abl. The 5' heterogeneity appears to be generated by alternative addition of 5' exons onto a common set of 3' exons. Alternative splicing occurs at the same site at which bcr sequences join to abl sequences in the Philadelphia chromosome translocation.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cloning, Molecular Gene Expression Regulation Genes Mice Proto-Oncogene Proteins/genetics Proto-Oncogenes RNA Processing, Post-Transcriptional RNA Splicing RNA, Messenger/genetics Tissue Distribution
Chemicals
Proto-Oncogene Proteins RNA, Messenger
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ben-Neriah Y
Bernards A
Paskind M
Daley G Q
Baltimore D
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1986-02-28
Pages
577-86
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · CA 38497 · United States
Databases
GENBANK
K03228, M12263, M12264, M12265, M12266
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