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Published November 2011 | Accepted Version
Journal Article Open

The mitochondrial transcription and packaging factor Tfam imposes a U-turn on mitochondrial DNA

Abstract

Tfam (transcription factor A, mitochondrial), a DNA-binding protein with tandem high-mobility group (HMG)-box domains, has a central role in the expression, maintenance and organization of the mitochondrial genome. It activates transcription from mitochondrial promoters and organizes the mitochondrial genome into nucleoids. Using X-ray crystallography, we show that human Tfam forces promoter DNA to undergo a U-turn, reversing the direction of the DNA helix. Each HMG-box domain wedges into the DNA minor groove to generate two kinks on one face of the DNA. On the opposite face, a positively charged α-helix serves as a platform to facilitate DNA bending. The structural principles underlying DNA bending converge with those of the unrelated HU family proteins, which have analogous architectural roles in organizing bacterial nucleoids. The functional importance of this extreme DNA bending is promoter specific and seems to be related to the orientation of Tfam on the promoters.

Additional Information

© 2011 Nature Publishing Group. Received 20 June 2011. Accepted 13 September 2011. Published online 30 October 2011. We thank N. Chan (California Institute of Technology) for making some mutant constructs, Y. Zhang and Z. Liu (California Institute of Technology) for suggestions on phase determination and structure refinement, T. Walton (California Institute of Technology) for advice on SEC-MALS, S. Shan (California Institute of Technology) for use of equipment and insightful discussions, the staff at the Stanford Synchrotron Radiation Lightsource (SSRL) for technical support with crystal screening and data collection, and members of the Chan laboratory for critical reading of the manuscript. We acknowledge the Gordon and Betty Moore Foundation for support of the Molecular Observatory at Caltech. SSRL is supported by the US Department of Energy and National Institutes of Health (NIH). This work was supported by NIH grants GM083121 (D.C.C.) and GM062967 (D.C.C.). Author Contributions: H.B.N. and D.C.C. designed the experiments, analyzed the data and wrote the paper. H.B.N. carried out the crystallography and performed the experimental work. J.T.K. helped with the crystallographic analysis.

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Created:
August 19, 2023
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