A nuclear factor that binds purine-rich, single-stranded oligonucleotides derived from S1-sensitive elements upstream of the CFTR gene and the MUC1 gene

Michael A. Hollingsworth*, Christina Closken, Ann Harris, Claudia D. Mcdonald, Gurcharan S. Pahwa, L. James Maher

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

We have identified two regions of non-random purine/pyrimldine strand asymmetry that were nearly identical in sequence in the 5′ flanking (promoter) regions of the human cystic fibrosis transmembrane conductance regulator (CFTR) gene and the human MUC1 gene. These regions contain perfect mirror repeat elements, a sequence motif previously found to be associated with the formation of H-DNA conformations. In this report we demonstrate that a single-stranded non-B DNA conformation exists at low pH in supercoiled plasmids containing the similar mirror repeat elements, and that S1 nuclease digestion maps the single-stranded region to the position of the mirror repeats. In addition, we identify a nuclear protein of approximately 27 kD that binds to single-stranded oligonucleotides corresponding to the purtne-rlch strand of this region, but not to the pyrlmldlne-rlch strands or to double-stranded oligonucleotides with corresponding purine/pyrimidlne strand asymmetry.

Original languageEnglish (US)
Pages (from-to)1138-1146
Number of pages9
JournalNucleic acids research
Volume22
Issue number7
DOIs
StatePublished - Apr 11 1994

Funding

The authors would like to thank Thomas Caffrey and John Skoog for technical assistance, and Tracy Culjat for secretarial assistance. This work was supported in part by the following grants: From the National Institutes of Health, DK44762, CA57362, GM47814 and CA36727; from the American Cancer Society, SIG 16; a grant from the Cystic Fibrosis Research Trust, UK; and by a Young Investigator's Award from Abbott Laboratories and a Junior Faculty Research Award from the American Cancer Society (both to L.J.M.)

ASJC Scopus subject areas

  • Genetics

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