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PMID: 3021337 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Alternative splicing of RNAs transcribed from the human abl gene and from the bcr-abl fused gene.

Cell ·Vol. 47 ·No. 2 ·1986-10-24 ·Pages 277-84

Shtivelman E, Lifshitz B, Gale RP, Roe BA, Canaani E

Abstract

The primary structure of normal abl protein was determined by sequencing the coding region of its cDNA. abl contains two alternative 5' exons spliced to a common set of 3' exons to yield the two major abl RNA transcripts. These transcripts initiate in different promoter regions and give rise to proteins that vary in their N-termini. In the human cell line K562, abl is translocated from chromosome 9 to within the bcr gene on chromosome 22. Within the fused bcr-abl gene, abl exon II alternatively splices to two adjacent bcr exons. This phenomenon is seen in many patients with chronic myeloid leukemia.

MeSH Terms
Abelson murine leukemia virus/genetics Amino Acid Sequence Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 9 DNA/genetics Exons Gene Expression Regulation Humans Leukemia Virus, Murine/genetics Leukemia, Myeloid/genetics Philadelphia Chromosome Promoter Regions, Genetic Proto-Oncogene Proteins/genetics Proto-Oncogenes RNA Splicing Translocation, Genetic
Chemicals
Proto-Oncogene Proteins DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shtivelman E
Lifshitz B
Gale R P
Roe B A
Canaani E
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1986-10-24
Pages
277-84
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · CA-38569 · United States
NIGMS NIH HHS · GM-30400 · United States
Databases
GENBANK
M14752, M14753, M14754, M14755, M15055
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