Map of chartreusin and elsamicin binding sites on DNA.

Abstract:

:Three DNA restriction fragments designated tyrT, 102-mer and 70-mer, have been used as substrates for footprinting studies using DNase I in the presence of the structurally similar antibiotics chartreusin and elsamicin A. The sequence-selective binding sites of the antibiotics can be mapped in regions which are rich in guanine + cytosine. Chartreusin and elsamicin appear to recognize and bind preferentially to sequences containing a CpG step. Regions containing a TpG step also seem to be a good binding site. The binding of elsamicin to these sites appears to be more concentration-dependent. A comparative analysis is performed of the sizes and locations of the different binding sites, aimed to infer whether the different biological effects of chartreusin and elsamicin A can be correlated to differences in their sequence-selective binding to DNA.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Salas X,Portugal J

doi

10.1016/0014-5793(91)80872-z

subject

Has Abstract

pub_date

1991-11-04 00:00:00

pages

223-8

issue

1-2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(91)80872-Z

journal_volume

292

pub_type

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