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PMID: 1730599 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Ku polypeptides synthesized in vitro assemble into complexes which recognize ends of double-stranded DNA.

The Journal of biological chemistry ·Vol. 267 ·No. 1 ·1992-01-05 ·Pages 331-8

Griffith AJ, Blier PR, Mimori T, Hardin JA

Abstract

The Ku protein is composed of two polypeptide subunits, p70 and p80, and binds DNA ends in vitro. Previous studies suggested that p70 and p80 are physically associated in vivo, although such an association may have been mediated by DNA. We have now utilized full-length Ku polypeptides synthesized in vitro to examine the association of p70, p80, and linear DNA to form a complex. In gel filtration chromatography, p70 migrates as a 70-kDa structure, whereas p80 migrates at 150 kDa. Co-translation of the two cDNAs yields complexes which migrate at 300 kDa and contain equimolar quantities of the p70 and p80 polypeptides, providing direct evidence that p70 and p80 assemble into a complex in the absence of DNA. To demonstrate that this recombinant protein complex binds DNA, we developed a radiolabeled protein electrophoretic mobility shift assay. When radiolabeled proteins synthesized in vitro were incubated with linear DNA and fractionated in a nonreducing, nondenaturing gel, a band representing a complex of p70, p80, and the DNA was seen. Formation of this Ku-DNA complex required free DNA ends, and binding to DNA ends was not observed with individual p70 or p80 subunits. DNA binding was not reconstituted by mixing the individual subunits together. These studies thus demonstrate that it is the complex of p70 and p80, not individual p70 or p80, which possesses the DNA binding properties previously described for native Ku protein. These results provide new information about the assembly, structure, and DNA binding properties of the Ku protein.

MeSH Terms
Antigens, Nuclear Chromatography, Gel Cloning, Molecular DNA/metabolism DNA Helicases DNA-Binding Proteins/biosynthesis,genetics,metabolism Electrophoresis, Polyacrylamide Gel Ku Autoantigen Nuclear Proteins/biosynthesis,genetics,metabolism Peptide Biosynthesis Peptides/genetics,metabolism Protein Binding Protein Biosynthesis Substrate Specificity Transcription, Genetic
Chemicals
Antigens, Nuclear DNA-Binding Proteins Nuclear Proteins Peptides DNA DNA Helicases XRCC5 protein, human Xrcc6 protein, human Ku Autoantigen
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Griffith A J
Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06510.
Blier P R
Mimori T
Hardin J A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-01-05
Pages
331-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIAID NIH HHS · AI26853 · United States
NIAMS NIH HHS · AR32549 · United States
NIAMS NIH HHS · AR40072 · United States
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