The long-term goal is to understand how the centrosome assembles and functions in animal cells. The centrosome is the major microtubule nucleating and organizing center that participates in organizing interphase cytoplasm and mitotic spindle poles. In mitosis, a bipolar spindle is organized efficiently from two centrosomes duplicated during S phase of the cell cycle. Recent studies suggested that mis-regulated centrosome duplication lead to mono- or multi-polar spindles and chromosome mis-segregation, linking cancer formation to centrosome dysfunction. Therefore, understanding the structure and function of the centrosome is relevant to human health. This grant seeks to study the mechanism of centrosome-mediated microtubule nucleation and centrosome assembly via studying a large protein complex, the gamma-tubulin ring complex (gammaTuRC) found at the centrosome. gammaTuRC is an important microtubule nucleator at the centrosome and it is required for centrosome assembly. In this granting period, we hope to understand 1) how gammaTuRC is assembled from multiple subunits, 2) how gammaTuRC functions in microtubule nucleation and organization, 3) how gammaTuRC is recruited to the centrosome to participate in microtubule nucleation and centrosome assembly.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM056312-07
Application #
6653829
Study Section
Special Emphasis Panel (ZRG1-CDF-4 (02))
Program Officer
Deatherage, James F
Project Start
1997-09-30
Project End
2006-08-31
Budget Start
2003-09-01
Budget End
2004-08-31
Support Year
7
Fiscal Year
2003
Total Cost
$183,178
Indirect Cost
Name
Carnegie Institution of Washington, D.C.
Department
Type
DUNS #
072641707
City
Washington
State
DC
Country
United States
Zip Code
20005
Huang, Yuejia; Li, Teng; Ems-McClung, Stephanie C et al. (2018) Aurora A activation in mitosis promoted by BuGZ. J Cell Biol 217:107-116
Zheng, Xiaobin; Hu, Jiabiao; Yue, Sibiao et al. (2018) Lamins Organize the Global Three-Dimensional Genome from the Nuclear Periphery. Mol Cell 71:802-815.e7
Gigante, Crystal M; Dibattista, Michele; Dong, Frederick N et al. (2017) Lamin B1 is required for mature neuron-specific gene expression during olfactory sensory neuron differentiation. Nat Commun 8:15098
Chen, Haiyang; Zheng, Xiaobin; Xiao, Danqing et al. (2016) Age-associated de-repression of retrotransposons in the Drosophila fat body, its potential cause and consequence. Aging Cell 15:542-52
Tran, Joseph R; Zheng, Xiaobin; Zheng, Yixian (2016) Lamin-B1 contributes to the proper timing of epicardial cell migration and function during embryonic heart development. Mol Biol Cell 27:3956-3963
Tran, Joseph R; Chen, Haiyang; Zheng, Xiaobin et al. (2016) Lamin in inflammation and aging. Curr Opin Cell Biol 40:124-130
Jiang, Hao; He, Xiaonan; Feng, Di et al. (2015) RanGTP aids anaphase entry through Ubr5-mediated protein turnover. J Cell Biol 211:7-18
Zheng, Xiaobin; Yue, Sibiao; Chen, Haiyang et al. (2015) Low-Cell-Number Epigenome Profiling Aids the Study of Lens Aging and Hematopoiesis. Cell Rep 13:1505-1518
Guo, Yuxuan; Zheng, Yixian (2015) Lamins position the nuclear pores and centrosomes by modulating dynein. Mol Biol Cell 26:3379-89
Zheng, Xiaobin; Kim, Youngjo; Zheng, Yixian (2015) Identification of lamin B-regulated chromatin regions based on chromatin landscapes. Mol Biol Cell 26:2685-97

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