The molecular architecture of the yeast spindle pole body core determined by Bayesian integrative modeling
Microtubule-organizing centers (MTOCs) form, anchor, and stabilize the polarized network of microtubules in a cell. The central MTOC is the centrosome that duplicates during the cell cycle and assembles a bipolar spindle during mitosis to capture and segregate sister chromatids. Yet, despite their i...
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Published in | Molecular biology of the cell Vol. 28; no. 23; pp. 3298 - 3314 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Cell Biology
07.11.2017
The American Society for Cell Biology |
Subjects | |
Online Access | Get full text |
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Summary: | Microtubule-organizing centers (MTOCs) form, anchor, and stabilize the polarized network of microtubules in a cell. The central MTOC is the centrosome that duplicates during the cell cycle and assembles a bipolar spindle during mitosis to capture and segregate sister chromatids. Yet, despite their importance in cell biology, the physical structure of MTOCs is poorly understood. Here we determine the molecular architecture of the core of the yeast spindle pole body (SPB) by Bayesian integrative structure modeling based on in vivo fluorescence resonance energy transfer (FRET), small-angle x-ray scattering (SAXS), x-ray crystallography, electron microscopy, and two-hybrid analysis. The model is validated by several methods that include a genetic analysis of the conserved PACT domain that recruits Spc110, a protein related to pericentrin, to the SPB. The model suggests that calmodulin can act as a protein cross-linker and Spc29 is an extended, flexible protein. The model led to the identification of a single, essential heptad in the coiled-coil of Spc110 and a minimal PACT domain. It also led to a proposed pathway for the integration of Spc110 into the SPB. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC5687031 Office of Science (SC), Biological and Environmental Research (BER) AC02-76SF00515; P01 GM105537; P41GM103393 USDOE Office of Science (SC), Basic Energy Sciences (BES) These authors contributed equally to this work. Department of Molecular and Cellular Biology, University of California at Davis, Davis, CA 95616. Department of Biochemistry, Vanderbilt University, 5110 MRB III, 465 21st Avenue South, Nashville, TN 37232 Present addresses: ‡Department of Neuroscience, University of Wisconsin–Madison, 1111 Highland Avenue, Madison, WI 53705 ǁDana-Farber Cancer Institute, Pedi Oncology M662B, 450 Brookline Avenue, Boston MA 02215 Author contributions: S.V., M.B., M.W., I.R., T.N.D., A.S., and E.G.M. designed the research. S.V. and M.B. performed the modeling. S.J.K., K.C.T., V.A.K., K.C.Y., N.T.U., H.A.V.E., J.M., M.H.J., D.R., T.N.D., and E.G.M. conducted the experiments. . V.A.K., M.W., I.R., T.N.D., and E.G.M. designed the experiments. S.V., M.B., S.J.K., H.A.V.E., J.M., J.AV-M., T.N.D., and E.G.M. analyzed the data. S.V., M.B., S.J.K., J.M., M.W., I.R., T.N.D., A.S., and E.G.M. wrote the paper. Translational Research, Seattle Genetics, Inc., Bothell, WA 98021 |
ISSN: | 1059-1524 1939-4586 |
DOI: | 10.1091/mbc.E17-06-0397 |