Name:Chuanhai Fu
Address:Room 205, Medical Sciences Building, School of

Life Sciences, 443 Huangshan road, Hefei, Anhui,

China 230027
Tel:0551-63600805
E-mail:chuanhai@ustc.edu.cn
EDUCATION AND RESEARCH EXPERIENCE
1997-2001University of Science and Technology of China, B.S.
1999-2001University of Science and Technology of China, B.E.
2001-2006University of Science and Technology of China, Ph.D.
2006-2011University of Pennsylvania, Postdoctoral Fellow
2011-2015The University of Hong Kong, Assistant Professor
2016-presentUniversity of Science and Technology of China, Professor
RESEARCH INTERESTS
(1) Microtubule dynamics
Microtubules are hollow tubular structures composed of 13 protofilaments within which α-,β-tubulin heterodimers bind to one another in a head-to-tail fashion. This structural arrangement confers the physical properties of polarity and dynamics to microtubules and thus allows microtubules to have a wide range of cellular functions including transporting organelles, directing cell motility, and mediating chromosome segregation. It is often found that microtubule associated proteins (MAPs) are expressed abnormally, and/or mutated, in tumor cells, making MAPs highly relevant to tumorigenesis. Hence, our research efforts are focused on investigating how MAPs are involved in regulating microtubule dynamics and mediating formation of the cell-type specific microtubule arrays.

(2) Mitochondria dynamics
Mitochondria are the powerhouse of a cell, constantly undergoing fusion and fission and intimately interacting with the cytoskeleton. Mitochondria malfunctions are associated with neuron degenerative diseases, aging, and tumorigenesis. Employing high spatiotemporal resolution microscopy, yeast genetics, and biochemistry, we aim to reveal the molecular mechanisms underlying mitochondria dynamics and regulating microtubule-mitochondria interactions.

(3) Mitosis
Mitosis is a fundamental process of life. During mitosis, chromosomes are segregated and equally divided into two daughter cells. Mitosis errors are usually correlated with failures of chromosome segregation, leading to more severe problems such as genomic instability, birth defects and cancer. My laboratory is interested in understanding the fundamental molecular mechanisms underlying spindle and chromosome dynamics during mitosis. We combine yeast genetics, quantitative live-cell imaging, biochemical and cell biological approaches to dissect organization, dynamics and regulation of the spindle in the fission yeast Schizosaccharomyces pombe.

SELECTED PUBLICATIONS
1.Shen J, Li T, Niu X, Liu W, Zheng S, Wang J, Wang F, Cao X, Yao X, Zheng F*, Fu C*. 2019. The J-domain cochaperone Rsp1 interacts with Mto1 to organize noncentrosomal microtubule assembly. Mol Biol Cell. 30(2):256-267 (*corresponding)
2.Zheng S, Dong F, Rasul F, Yao X, Jin QW, Zheng F*, Fu C*. 2018. Septins regulate the equatorial dynamics of the separation initiation network kinase Sid2p and glucan synthases to ensure proper cytokinesis. FEBS J. 285(13):2468-2480 (*corresponding)
3.Zhu Q, Zheng F, Liu AP, Qian J, Fu C*, Lin Y*. 2016. Shape Transformation of the Nuclear Envelope during Closed Mitosis. Biophys J. 111(10):2309-2316 (*corresponding)
4.Li T, Zheng F, Cheung M, Wang F, Fu C*. 2015. Fission yeast mitochondria are distributed by dynamic microtubules in a motor-independent manner. Sci Rep. 5:11023 (*corresponding)
5.Zheng F, Li T, Jin D, Syrovatkina V, Scheffler K, Tran PT*, Fu C*. 2014. Csi1p recruits alp7p/TACC to the SPB for bipolar spindle formation. Mol Biol Cell. 25(18):2750-60. (*corresponding)
6.Zheng F, Li T, Cheung M, Syrovatkina V, Fu C*. 2014. Mcp1p tracks microtubule plus ends to destabilize microtubules at cell tips. FEBS Lett. 2014 Mar 18;588(6):859-65 (*corresponding) (cover story)
7.Syrovatkina V#, Fu C#, Tran PT. 2013. Antagonistic spindle motors and MAPs regulate metaphase spindle length and chromosome segregation. Curr Biol. 23: 2423-9 (#cofirst)
8.Fu C*, Jain D, Costa J, Velve-Casquillas G, Tran PT*. 2011. Mmb1p binds mitochondria to dynamic microtubules. Curr Biol. 21:1431-39 (*corresponding)
9.Fu C, Ward JJ, Loiodice I, Velve-Casquillas G, Nedelec FJ, Tran PT. 2009. Phospho-regulated interaction between kinesin-6 Klp9p and microtubule bundler Ase1p promotes spindle elongation. Dev Cell 17: 257-67
10.Fu C, Yan F, Wu F, Wu Q, Whittaker J, Hu H, Hu R, Yao X. 2007. Mitotic phosphorylation of PRC1 at Thr470 is required for PRC1 oligomerization and proper central spindle organization. Cell Res 17: 449-57
11.Fu C, Ahmed K, Ding H, Ding X, Lan J, Yang Z, Miao Y, Zhu Y, Shi Y, Zhu J, Huang H, Yao X. 2005. Stabilization of PML nuclear localization by conjugation and oligomerization of SUMO-3. Oncogene 24: 5401-13

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