The pseudodisaccharides: a novel class of group I intron splicing inhibitors.

Abstract:

:Lysinomicin, a naturally-occurring pseudodisaccharide, inhibits translation in prokaryotes. We report that lysinomicin (and three related compounds) are able to inhibit the self-splicing of group I introns, thus identifying pseudodisaccharides as a novel class of group I intron splicing inhibitors. Lysinomicin inhibited the self-splicing of the sunY intron of phage T4 with a Ki of 8.5 microM (+/- 5 microM) and was active against other group I introns. Inhibition was found to be competitive with the substrate guanosine, unlike aminoglycoside antibiotics, which act non-competitively to inhibit the splicing of group I introns. Competitive inhibitors of group I intron splicing known to date all contain a guanidino group that was thought to be required for inhibition; lysinomicin lacks a guanidino group.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Rogers J,Davies J

doi

10.1093/nar/22.23.4983

subject

Has Abstract

pub_date

1994-11-25 00:00:00

pages

4983-8

issue

23

eissn

0305-1048

issn

1362-4962

journal_volume

22

pub_type

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