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Specific targeting of protein–DNA complexes by dna‐reactive drugs (+)‐CC‐1065 and pluramycins
Author(s) -
Henderson Douglas,
Hurley Laurence H.
Publication year - 1996
Publication title -
journal of molecular recognition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.401
H-Index - 79
eISSN - 1099-1352
pISSN - 0952-3499
DOI - 10.1002/(sici)1099-1352(199603)9:2<75::aid-jmr247>3.0.co;2-4
Subject(s) - base pair , dna , tata box , microbiology and biotechnology , transcription (linguistics) , dna clamp , dna footprinting , hmg box , tata binding protein , protein–dna interaction , chemistry , tata box binding protein , general transcription factor , biology , promoter , biophysics , rna , transcription factor , biochemistry , dna binding protein , gene , reverse transcriptase , gene expression , linguistics , philosophy
To gain insight into the interactions between transcriptional factor proteins and DNA, the DNA‐reactive drugs (+)‐CC‐1065 and pluramycin were used to target specific protein–DNA complexes. The structural features of the complex between the transcriptional activator Sp1 and the 21‐base‐pair repeat of the early promoter region of SV40 DNA were examined using hydroxyl‐radical footprinting; (+)‐CC‐1065, a sequence‐specific minor groove bending probe; and circularization experiments. The results show that the 21‐base‐pair repeat region has an intrinsically in‐phase bent structure that is stabilized upon saturation Sp1 binding by protein–DNA and protein–protein interactions to produce a looping structure. The intercalating drug pluramycin was used to probe the structural details of the interaction between the TATA binding protein (TBP) and the TATA box DNA sequence. TBP, which directs initiation of RNA transcription, exhibits two‐fold symmetry and apparently interacts with the TATA box in a symmetrical fashion. However, the interaction results in an asymmetric effect, in that transcription is initiated only in the downstream direction. Using pluramycin as a probe, it was determined that TBP binding to the human myoglobin TATA sequences enhances pluramycin reactivity at a site immediately downstream of the TATA box. The implications on transcriptional control of ternary complexes comprised of transcriptional factors, DNA, and DNA‐reactive compounds will be presented.