scholarly journals Haspin kinase regulates microtubule-organizing center clustering and stability through Aurora kinase C in mouse oocytes

2016 ◽  
Vol 129 (19) ◽  
pp. 3648-3660 ◽  
Author(s):  
Ahmed Z. Balboula ◽  
Alexandra L. Nguyen ◽  
Amanda S. Gentilello ◽  
Suzanne M. Quartuccio ◽  
David Drutovic ◽  
...  
2020 ◽  
Vol 31 (12) ◽  
pp. 1206-1217
Author(s):  
Tara M. Little ◽  
Philip W. Jordan

By deleting Plk1 in mouse oocytes before meiotic resumption, we show that PLK1 is essential for the formation of condensed bivalent chromosomes, microtubule organizing center fragmentation, liquid-like spindle domain localization, and bipolar spindle formation. Thus, PLK1 coordinates processes that ensure chromosome segregation during meiosis I.


PLoS ONE ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. e94708 ◽  
Author(s):  
Hyejin Shin ◽  
Sojung Kwon ◽  
Haengseok Song ◽  
Hyunjung Jade Lim

Author(s):  
M.B. Braunfeld ◽  
M. Moritz ◽  
B.M. Alberts ◽  
J.W. Sedat ◽  
D.A. Agard

In animal cells, the centrosome functions as the primary microtubule organizing center (MTOC). As such the centrosome plays a vital role in determining a cell's shape, migration, and perhaps most importantly, its division. Despite the obvious importance of this organelle little is known about centrosomal regulation, duplication, or how it nucleates microtubules. Furthermore, no high resolution model for centrosomal structure exists.We have used automated electron tomography, and reconstruction techniques in an attempt to better understand the complex nature of the centrosome. Additionally we hope to identify nucleation sites for microtubule growth.Centrosomes were isolated from early Drosophila embryos. Briefly, after large organelles and debris from homogenized embryos were pelleted, the resulting supernatant was separated on a sucrose velocity gradient. Fractions were collected and assayed for centrosome-mediated microtubule -nucleating activity by incubating with fluorescently-labeled tubulin subunits. The resulting microtubule asters were then spun onto coverslips and viewed by fluorescence microscopy.


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