Poisoning of mitochondrial topoisomerase I by lamellarin D.
Journal: 2014/August - Molecular Pharmacology
ISSN: 1521-0111
Abstract:
Lamellarin D (Lam-D) is a hexacyclic pyrole alkaloid isolated from marine invertebrates, whose biologic properties have been attributed to mitochondrial targeting. Mitochondria contain their own DNA (mtDNA), and the only specific mitochondrial topoisomerase in vertebrates is mitochondrial topoisomerase I (Top1mt). Here, we show that Top1mt is a direct mitochondrial target of Lam-D. In vitro Lam-D traps Top1mt and induces Top1mt cleavage complexes (Top1mtcc). Using single-molecule analyses, we also show that Lam-D slows down supercoil relaxation of Top1mt and strongly inhibits Top1mt religation in contrast to the inefficacy of camptothecin on Top1mt. In living cells, we show that Lam-D accumulates rapidly inside mitochondria, induces cellular Top1mtcc, and leads to mtDNA damage. This study provides evidence that Top1mt is a direct mitochondrial target of Lam-D and suggests that developing Top1mt inhibitors represents a novel strategy for targeting mitochondrial DNA.
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Mol Pharmacol 86(2): 193-199

Poisoning of Mitochondrial Topoisomerase I by Lamellarin D

Developmental Therapeutics Branch and Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute (S.K., K.A., I.D.R., S.A., K.F., H.Z., Y.P.) and Laboratory of Molecular Biophysics, National Heart, Lung, and Blood Institute (Y.S., K.C.N.), National Institutes of Health, Bethesda, Maryland
Corresponding author.
Address correspondence to: Dr. Yves Pommier, Laboratory of Molecular Pharmacology and Developmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bldg. 37, Rm. 5068, 37 Convent Drive, MSC 4255, Bethesda, MD 20814., E-mail: vog.hin@reimmop
Received 2014 Mar 21; Accepted 2014 May 28.

Abstract

Lamellarin D (Lam-D) is a hexacyclic pyrole alkaloid isolated from marine invertebrates, whose biologic properties have been attributed to mitochondrial targeting. Mitochondria contain their own DNA (mtDNA), and the only specific mitochondrial topoisomerase in vertebrates is mitochondrial topoisomerase I (Top1mt). Here, we show that Top1mt is a direct mitochondrial target of Lam-D. In vitro Lam-D traps Top1mt and induces Top1mt cleavage complexes (Top1mtcc). Using single-molecule analyses, we also show that Lam-D slows down supercoil relaxation of Top1mt and strongly inhibits Top1mt religation in contrast to the inefficacy of camptothecin on Top1mt. In living cells, we show that Lam-D accumulates rapidly inside mitochondria, induces cellular Top1mtcc, and leads to mtDNA damage. This study provides evidence that Top1mt is a direct mitochondrial target of Lam-D and suggests that developing Top1mt inhibitors represents a novel strategy for targeting mitochondrial DNA.

Abstract

Acknowledgments

The authors thank Dr. Carmen Cuevas Marchante and José M. Fernandez Sousa-Faro, PharmaMar, for providing lamellarin D.

Acknowledgments

Abbreviations

CPTCamptothecin
ICEimmuno-complex of enzyme
Lam-Dlamellarin D
mtDNAmitochondrial DNA
NCI_H23adenocarcinoma, human non–small cell lung cancer
SK-MEL-5human skin melanoma cell line
Top1topoisomerase I
Top1ccTop1 cleavage complexes
Top1mtmitochondrial topoisomerase I
Top1mtccmitochondrial topoisomerase I cleavage complexes
Twtwist density
Abbreviations

Authorship Contributions

Participated in research design: Khiati, Seol, Agama, Dalla Rosa, Zhang, Neuman, Pommier.

Conducted experiments: Khiati, Seol, Agama, Agrawal, Fesen.

Performed data analysis: Khiati, Seol, Agama, Dalla Rosa, Neuman, Pommier.

Wrote or contributed to the writing of the manuscript: Khiati, Seol, Agama, Dalla Rosa, Neuman, Pommier.

Authorship Contributions

Footnotes

This work was supported by the Intramural Research Program of the National Institutes of Health National Cancer Institute, Center of Cancer Research [Z01 BC006161] and the National Heart, Lung, and Blood Institute.

dx.doi.org/10.1124/mol.114.092833.

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