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PMID: 3651409 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Chemical determinants of DNA bending at adenine-thymine tracts.

Biochemistry ·Vol. 26 ·No. 12 ·1987-06-16 ·Pages 3745-8

Koo HS, Crothers DM

Abstract

DNA fragments having homopolymeric adenine-thymine tracts phased with the helix screw are known to be bent. According to our working model, adenine-thymine tracts adopt a polymorphic structure (H-DNA), and juxtaposition of H-DNA with B-DNA results in bending at the junction between the two structures. We incorporated different base analogues in addition to the four ordinary bases into oligonucleotides; ligated multimers of oligonucleotide duplexes were run on polyacrylamide gels. By comparison of gel mobility data for different sequences, we identified factors both necessary and irrelevant for bending, corresponding to the formation of H-DNA. The 5-methyl group on pyrimidines is not essential, and the 2-amino group on purines interferes with the formation of H-DNA, either because it provides a third H bond between the bases or because it alters water structure in the minor groove. The strong base stacking of A may be an important contributing factor to stabilization of the anomalous DNA structure responsible for bending.

MeSH Terms
Adenine Base Composition DNA Hydrogen Bonding Nucleic Acid Conformation Oligodeoxyribonucleotides Thymine
Chemicals
Oligodeoxyribonucleotides DNA Adenine Thymine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Koo H S
Department of Chemistry, Yale University, New Haven, Connecticut 06511.
Crothers D M
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1987-06-16
Pages
3745-8
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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