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PMID: 3027700 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Efficient and stable expression of recombinant fibronectin polypeptides.

Schwarzbauer JE, Mulligan RC, Hynes RO

Abstract

We describe retroviral expression vectors containing cDNAs encoding part of fibronectin preceded by the signal and "pro" sequences of parathyroid hormone. The recombinant retroviruses were used to generate NIH 3T3 cell lines stably producing functionally active fragments of fibronectin. The recombinant fibronectins (deminectins) are processed and secreted by the cells and form disulfide-bonded dimers with themselves and with endogenous fibronectin subunits. The fibronectin-deminectin heterodimers are incorporated into the extracellular matrix. We describe cell lines producing six variant forms of deminectin corresponding to variant forms of fibronectin produced by alternative splicing. In constructing fibronectin cDNAs encoding the six variant forms, we also made use of the ability of retroviral vectors to generate cDNAs by accurate splicing of cloned genomic segments. These constructs should be valuable in analyses of the structure-function relationships of fibronectins.

MeSH Terms
Animals Cell Line Cloning, Molecular DNA/metabolism DNA Restriction Enzymes Extracellular Matrix/metabolism Fibronectins/biosynthesis,genetics Liver/metabolism Promoter Regions, Genetic Rats Recombinant Proteins/metabolism
Chemicals
Fibronectins Recombinant Proteins DNA DNA Restriction Enzymes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schwarzbauer J E
Mulligan R C
Hynes R O
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25 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1987-02-00
Pages
754-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC304294
Subset
IM
Grants
NCI NIH HHS · P01-CA 26712 · United States
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