Mithramycin blocks protein binding and function of the SV40 early promoter
- PMID: 2542379
- PMCID: PMC303924
- DOI: 10.1172/JCI114110
Mithramycin blocks protein binding and function of the SV40 early promoter
Abstract
Specific interactions between DNA and transcription factors are necessary for transcription initiation. These interactions provide a potential target for the selective inhibition of eukaryotic gene expression. Mithramycin is a DNA binding antibiotic which, in the presence of Mg2+, binds G-C containing sequences in the minor groove. The SV40 early promoter contains six G-C decanucleotide sequences, which are binding sites for the transcriptional activating factor, Sp1. Each of the six Sp1 binding sites of this promoter is protected from DNAse 1 digestion by mithramycin binding. Mithramycin binding to the G-C rich sequences in the SV40 early promoter prevents subsequent protein binding to these sequences. The gel retardation of the SV40 early promoter fragment incubated with a HeLa cell extract is completely abrogated by pretreatment of the DNA fragment with mithramycin. The functional significance of mithramycin binding is reflected in the ability of mithramycin to block promoter function. Mithramycin inhibits promoter dependent transcription in an in vitro runoff transcription system in a concentration dependent manner. This suggests that mithramycin prevents transcriptional activation of the SV40 early promoter by blocking binding of transcriptional activating proteins to G-C rich promoter regions.
Similar articles
-
Mithramycin blocks transcriptional initiation of the c-myc P1 and P2 promoters.Biochemistry. 1991 Apr 30;30(17):4290-7. doi: 10.1021/bi00231a027. Biochemistry. 1991. PMID: 1827033
-
Mithramycin inhibits SP1 binding and selectively inhibits transcriptional activity of the dihydrofolate reductase gene in vitro and in vivo.J Clin Invest. 1991 Nov;88(5):1613-21. doi: 10.1172/JCI115474. J Clin Invest. 1991. PMID: 1834700 Free PMC article.
-
Inhibition of c-src transcription by mithramycin: structure-activity relationships of biosynthetically produced mithramycin analogues using the c-src promoter as target.Biochemistry. 2003 Jul 15;42(27):8313-24. doi: 10.1021/bi034091z. Biochemistry. 2003. PMID: 12846580
-
Regulation of SV40 early gene expression.Biochem Cell Biol. 1988 Jun;66(6):567-77. doi: 10.1139/o88-067. Biochem Cell Biol. 1988. PMID: 2844212 Review.
-
Mithramycin and its analogs: Molecular features and antitumor action.Pharmacol Ther. 2024 Aug;260:108672. doi: 10.1016/j.pharmthera.2024.108672. Epub 2024 Jun 3. Pharmacol Ther. 2024. PMID: 38838821 Review.
Cited by
-
Genetic diversity and striatal gene networks: focus on the heterogeneous stock-collaborative cross (HS-CC) mouse.BMC Genomics. 2010 Oct 19;11:585. doi: 10.1186/1471-2164-11-585. BMC Genomics. 2010. PMID: 20959017 Free PMC article.
-
Ketopremithramycins and ketomithramycins, four new aureolic acid-type compounds obtained upon inactivation of two genes involved in the biosynthesis of the deoxysugar moieties of the antitumor drug mithramycin by Streptomyces argillaceus, reveal novel insights into post-PKS tailoring steps of the mithramycin biosynthetic pathway.J Am Chem Soc. 2002 Feb 27;124(8):1606-14. doi: 10.1021/ja0105156. J Am Chem Soc. 2002. PMID: 11853433 Free PMC article.
-
Decitabine Inhibits Gamma Delta T Cell Cytotoxicity by Promoting KIR2DL2/3 Expression.Front Immunol. 2018 Mar 26;9:617. doi: 10.3389/fimmu.2018.00617. eCollection 2018. Front Immunol. 2018. PMID: 29632540 Free PMC article.
-
Alterations in the regulation of expression of the alpha 1(I) collagen gene (COL1A1) in systemic sclerosis (scleroderma).Springer Semin Immunopathol. 1999;21(4):397-414. doi: 10.1007/BF00870302. Springer Semin Immunopathol. 1999. PMID: 10945033 Review.
-
VIP Induces Changes in the F-/G-Actin Ratio of Schlemm's Canal Endothelium via LRRK2 Transcriptional Regulation.Invest Ophthalmol Vis Sci. 2020 Jun 3;61(6):45. doi: 10.1167/iovs.61.6.45. Invest Ophthalmol Vis Sci. 2020. PMID: 32572455 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous