A structural analysis of the bent kinetoplast DNA from Crithidia fasciculata by high resolution chemical probing

The chemical probes potassium permanganate (KMnO4) and diethylpyrocarbonate (DEPC) have been used to study the conformation of bent kinetoplast DNA from Crithidia fasciculata at different temperatures. Chemical reactivity data shows that the numerous short A-tracts of this bent DNA adopt a similar s...

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Published inNucleic acids research Vol. 21; no. 14; pp. 3309 - 3317
Main Authors McCarthy, James G., Frederick, Christine A., Nicolas, Alain
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 11.07.1993
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Summary:The chemical probes potassium permanganate (KMnO4) and diethylpyrocarbonate (DEPC) have been used to study the conformation of bent kinetoplast DNA from Crithidia fasciculata at different temperatures. Chemical reactivity data shows that the numerous short A-tracts of this bent DNA adopt a similar structure at 43°C. This conformation appears to be very similar to the conformation of A-tracts in DNA exhibiting normal gel mobility. The A-tract structure detected by chemical probing is characterized by a high degree of base stacking on the thymlne strand, and by an abrupt conformational change at the 3' end of the adenlne strand. In general, no major alteration of this A-tract specific structure was detected between 4-53°C. However, probing with KMnO4 revealed two unusual features of the C. fasciculata sequence that may contribute to the highly aberrant gel mobility of this DNA: 1) the B DNA/A-tract Junction 5' dC/A38 3'. 5' dT3e/G 3' is disproportionately represented and is conformationally distinct from other 5' end junctions, and 2) low temperature favors a novel strand-specific conformational distortion over a 20 base pair region of the bent kinetoplast DNA. Presence of the minor groove binding drug dlstamycln had little detectable effect on the A-tract conformation. However, distamycin did inhibit formation of the novel KMnO4 sensitive low temperature structure and partially eliminated the anomalous gel mobility of the kinetoplast DNA. Finally, we describe a simple and reproducible procedure for the production of an adenlne-speciflc chemical DNA sequence ladder.
Bibliography:ark:/67375/HXZ-NLL5TQPL-S
istex:CE6EADFE9DF1A079BDF671C9F173C177B7246A8B
1To whom correspondence should be addressed at: Westreco Inc., 201 Housatonic Ave, New Milford, CT, 06776, USA
ArticleID:21.14.3309
ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0305-1048
1362-4962
DOI:10.1093/nar/21.14.3309