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Interaction of bleomycin with a bent DNA fragment

Interaction of bleomycin with a bent DNA fragment
Interaction of bleomycin with a bent DNA fragment

The interaction of bleomycin with a kinetoplast DNA fragment has been examined using various footprinting techniques. This DNA adopts a bent structure and displays an unusually low gel mobility on account of its phased runs of adenines. The bleomycin-cobalt complex increases the mobility of this DNA fragment, in contrast with other DNAs which show a decreased rate of gel migration, suggesting that the antibiotic removes DNA bending, possibly via an unwinding mechanism. Removal of the bending is confirmed by hydroxy-radical footprinting which produces a more even ladder of bands in the presence of the ligand. Cleavage by bleomycin is at the sequence G-pyrimidine, though not all such sites are affected to the same extent and some cutting is found at GA and GG. DNAase I footprinting confirms the antibiotic-binding sites but reveals that some strong cleavage sites do not yield footprints. Bleomycin renders adenines on the 3' side of its cleavage sites (GT, GC and GA) hyper-reactive to diethyl pyrocarbonate.

0264-6021
929-934
Nightingale, K. P.
a3a1d01a-fcb3-4877-9752-4b0f047b6779
Fox, K. R.
9da5debc-4e45-473e-ab8c-550d1104659f
Nightingale, K. P.
a3a1d01a-fcb3-4877-9752-4b0f047b6779
Fox, K. R.
9da5debc-4e45-473e-ab8c-550d1104659f

Nightingale, K. P. and Fox, K. R. (1992) Interaction of bleomycin with a bent DNA fragment. Biochemical Journal, 284 (3), 929-934. (doi:10.1042/bj2840929).

Record type: Article

Abstract

The interaction of bleomycin with a kinetoplast DNA fragment has been examined using various footprinting techniques. This DNA adopts a bent structure and displays an unusually low gel mobility on account of its phased runs of adenines. The bleomycin-cobalt complex increases the mobility of this DNA fragment, in contrast with other DNAs which show a decreased rate of gel migration, suggesting that the antibiotic removes DNA bending, possibly via an unwinding mechanism. Removal of the bending is confirmed by hydroxy-radical footprinting which produces a more even ladder of bands in the presence of the ligand. Cleavage by bleomycin is at the sequence G-pyrimidine, though not all such sites are affected to the same extent and some cutting is found at GA and GG. DNAase I footprinting confirms the antibiotic-binding sites but reveals that some strong cleavage sites do not yield footprints. Bleomycin renders adenines on the 3' side of its cleavage sites (GT, GC and GA) hyper-reactive to diethyl pyrocarbonate.

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Published date: 1992

Identifiers

Local EPrints ID: 475588
URI: http://eprints.soton.ac.uk/id/eprint/475588
ISSN: 0264-6021
PURE UUID: 7b6dbc80-79c3-4352-bc1d-291f060481f5
ORCID for K. R. Fox: ORCID iD orcid.org/0000-0002-2925-7315

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Date deposited: 22 Mar 2023 17:31
Last modified: 17 Mar 2024 02:34

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Contributors

Author: K. P. Nightingale
Author: K. R. Fox ORCID iD

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