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Published October 2011 | public
Journal Article

MamK, a bacterial actin, forms dynamic filaments in vivo that are regulated by the acidic proteins MamJ and LimJ

Abstract

Bacterial actins, in contrast to their eukaryotic counterparts, are highly divergent proteins whose wideranging functions are thought to correlate with their evolutionary diversity. One clade, represented by the MamK protein of magnetotactic bacteria, is required for the subcellular organization of magnetosomes, membrane-bound organelles that aid in navigation along the earth's magnetic field. Using a fluorescence recovery after photobleaching assay in Magnetospirillum magneticum AMB-1, we find that, like traditional actins, MamK forms dynamic filaments that require an intact NTPase motif for their turnover in vivo. We also uncover two proteins, MamJ and LimJ, which perform a redundant function to promote the dynamic behaviour of MamK filaments in wild-type cells. The absence of both MamJ and LimJ leads to static filaments, a disrupted magnetosome chain, and an anomalous build-up of cytoskeletal filaments between magnetosomes. Our results suggest that MamK filaments, like eukaryotic actins, are intrinsically stable and rely on regulators for their dynamic behaviour, a feature that stands in contrast to some classes of bacterial actins characterized to date.

Additional Information

© 2011 Blackwell Publishing Ltd. Accepted 18 August, 2011. Article first published online: 14 Sep 2011. We thank the members of the Komeili laboratory for their valuable research and editorial input. O.D., M.B., and S.K. thank Steve Ruzin and Denise Schichnes at the UC Berkeley Biological Imaging Facility. O.D. and J.C. thank Kent McDonald and Reena Zalpuri at the Robert D. Ogg Electron Microscope Lab. Z.L. thanks Alasdair McDowall and Martin Pilhofer for help with data collection. The cryotomography work was supported by NIH grant R01 GM094800B to G.J.J. A.K. was supported through grants from the Packard Foundation and the National Institutes of Health (R01GM084122).

Additional details

Created:
August 19, 2023
Modified:
October 24, 2023