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PMID: 2541919 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A putative murine ecotropic retrovirus receptor gene encodes a multiple membrane-spanning protein and confers susceptibility to virus infection.

Cell ·Vol. 57 ·No. 4 ·1989-05-19 ·Pages 659-66

Albritton LM, Tseng L, Scadden D, Cunningham JM

Abstract

Murine type C ecotropic retrovirus infection is initiated by virus envelope binding to a membrane receptor expressed on mouse cells. We have identified a cDNA clone that may encode for this receptor through a strategy combining gene transfer of mouse NIH 3T3 DNA into nonpermissive human EJ cells, selection of EJ clones that have acquired susceptibility to infection by retrovirus vectors containing drug resistance genes, and identification of the putative receptor cDNA clone through linkage to a mouse repetitive DNA sequence. Human EJ cells that express the cDNA acquire a million-fold increase in MuLV infectivity. The predicted 622 amino acid sequence of the putative receptor protein is extremely hydrophobic; 14 potential membrane-spanning domains have been identified. A computer-based search of sequence data banks did not identify a protein with significant similarity to the putative receptor. We conclude that a novel membrane protein determines susceptibility to ecotropic MuLV infection by binding and/or fusion with the virus envelope.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Line Cloning, Molecular DNA/analysis,genetics Disease Susceptibility Gene Expression Regulation Genetic Vectors Membrane Proteins/genetics,physiology Mice Molecular Sequence Data Retroviridae Infections/immunology Retroviridae Proteins/genetics Transcription, Genetic Transfection Tumor Cells, Cultured Urinary Bladder Neoplasms/pathology,ultrastructure
Chemicals
Membrane Proteins Retroviridae Proteins DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Albritton L M
Howard Hughes Medical Institute, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
Tseng L
Scadden D
Cunningham J M
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1989-05-19
Pages
659-66
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NHLBI NIH HHS · 5 T32 HL07623 · United States
Databases
GENBANK
M26687
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