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PMID: 2895474 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Isolation and sequencing of a cDNA coding for the human DF3 breast carcinoma-associated antigen.

Siddiqui J, Abe M, Hayes D, Shani E, Yunis E, Kufe D

Abstract

The murine monoclonal antibody (mAb) DF3 reacts with a high molecular weight glycoprotein detectable in human breast carcinomas. DF3 antigen expression correlates with human breast tumor differentiation, and the detection of a cross-reactive species in human milk has suggested that this antigen might be useful as a marker of differentiated mammary epithelium. To further characterize DF3 antigen expression, we have isolated a cDNA clone from a lambda gt11 library by screening with mAb DF3. The results demonstrate that this 309-base-pair cDNA, designated pDF9.3, codes for the DF3 epitope. Southern blot analyses of EcoRI-digested DNAs from six human tumor cell lines with 32P-labeled pDF9.3 have revealed a restriction fragment length polymorphism. Variations in size of the alleles detected by pDF9.3 were also identified in Pst I, but not in HindIII, DNA digests. Furthermore, hybridization of 32P-labeled pDF9.3 with total cellular RNA from each of these cell lines demonstrated either one or two transcripts that varied from 4.1 to 7.1 kilobases in size. The presence of differently sized transcripts detected by pDF9.3 was also found to correspond with the polymorphic expression of DF3 glycoproteins. Nucleotide sequence analysis of pDF9.3 has revealed a highly conserved (G + C)-rich 60-base-pair tandem repeat. These findings suggest that the variation in size of alleles coding for the polymorphic DF3 glycoprotein may represent different numbers of repeats.

MeSH Terms
Antibodies, Monoclonal/immunology Antibodies, Neoplasm/immunology Antigens, Neoplasm/genetics Base Sequence Breast Neoplasms/genetics,immunology DNA/genetics Humans Molecular Sequence Data Polymorphism, Restriction Fragment Length Tumor Cells, Cultured/immunology
Chemicals
Antibodies, Monoclonal Antibodies, Neoplasm Antigens, Neoplasm DNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Siddiqui J
Laboratory of Clinical Pharmacology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.
Abe M
Hayes D
Shani E
Yunis E
Kufe D
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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
1988-04-00
Pages
2320-3
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC279983
Subset
IM
Grants
NCI NIH HHS · CA-20531 · United States
NCI NIH HHS · CA-38869 · United States
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