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PMID: 2670246 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The mouse type IV c-abl gene product is a nuclear protein, and activation of transforming ability is associated with cytoplasmic localization.

Cell ·Vol. 58 ·No. 4 ·1989-08-25 ·Pages 669-78

Van Etten RA, Jackson P, Baltimore D

Abstract

The subcellular localization of the mouse type IV c-abl protein was determined by indirect immunofluorescence of nontransformed NIH 3T3 fibroblasts that overexpress the protein. Unlike the viral transforming protein p160gag/v-abl, which has cytoplasmic and plasma membrane localization, a large fraction of the c-abl (IV) protein is nuclear, with the remainder in the cytoplasm and plasma membrane. Deletion of a small N-terminal regulatory region of the c-abl (IV) protein, sufficient to activate its transforming potential fully, changes the distribution of the protein from the nucleus to the cytoplasm. Mapping of an amino acid sequence responsible for the nuclear localization of the c-abl (IV) protein reveals a nuclear localization signal similar to that of SV40 large T antigen.

MeSH Terms
Amino Acid Sequence Animals Cell Compartmentation Cell Line Cell Membrane/metabolism Cytoplasm/metabolism DNA Mutational Analysis Fluorescent Antibody Technique Mice Molecular Sequence Data Myristic Acid Myristic Acids/physiology Nuclear Proteins/physiology,ultrastructure Protein Processing, Post-Translational Proto-Oncogene Proteins/physiology,ultrastructure Proto-Oncogene Proteins c-abl
Chemicals
Myristic Acids Nuclear Proteins Proto-Oncogene Proteins Myristic Acid Proto-Oncogene Proteins c-abl
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Van Etten R A
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
Jackson P
Baltimore D
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1989-08-25
Pages
669-78
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · CA38497 · United States
NHLBI NIH HHS · T32HL07623 · United States
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