Nivalenol affects spindle formation and organelle functions during mouse oocyte maturation

Author(s):  
Yue Wang ◽  
Zhen-Nan Pan ◽  
Chun-Hua Xing ◽  
Hao-Lin Zhang ◽  
Shao-Chen Sun
2013 ◽  
Vol 25 (3) ◽  
pp. 495 ◽  
Author(s):  
Ya-Peng Wang ◽  
Shu-Tao Qi ◽  
Yanchang Wei ◽  
Zhao-Jia Ge ◽  
Lei Chen ◽  
...  

UCHL5IP is one of the subunits of the haus complex, which is important for microtubule generation, spindle bipolarity and accurate chromosome segregation in Drosophila and human mitotic cells. In this study, the expression and localisation of UCHL5IP were explored, as well as its functions in mouse oocyte meiotic maturation. The results showed that the UCHL5IP protein level was consistent during oocyte maturation and it was localised to the meiotic spindle in MI and MII stages. Knockdown of UCHL5IP led to spindle defects, chromosome misalignment and disruption of γ-tubulin localisation in the spindle poles. These results suggest that UCHL5IP plays critical roles in spindle formation during mouse oocyte meiotic maturation.


2018 ◽  
Vol 32 (2) ◽  
pp. 625-638 ◽  
Author(s):  
In‐Won Lee ◽  
Yu‐Jin Jo ◽  
Seung‐Min Jung ◽  
Hai‐Yang Wang ◽  
Nam‐Hyung Kim ◽  
...  

2013 ◽  
Vol 19 (5) ◽  
pp. 1364-1373 ◽  
Author(s):  
Jie Zhao ◽  
Lu Wang ◽  
Hong-Xia Zhou ◽  
Li Liu ◽  
Angeleem Lu ◽  
...  

AbstractClathrin heavy chain 1 (CLTC) has been considered a “moonlighting protein” which acts in membrane trafficking during interphase and in stabilizing spindle fibers during mitosis. However, its roles in meiosis, especially in mammalian oocyte maturation, remain unclear. This study investigated CLTC expression and function in spindle formation and chromosome congression during mouse oocyte meiotic maturation. Our results showed that the expression level of CLTC increased after germinal vesicle breakdown (GVBD) and peaked in the M phase. Immunostaining results showed CLTC distribution throughout the cytoplasm in a cell cycle-dependent manner. Appearance and disappearance of CLTC along with β-tubulin (TUBB) could be observed during spindle dynamic changes. To explore the relationship between CLTC and microtubule dynamics, oocytes at metaphase were treated with taxol or nocodazole. CLTC colocalized with TUBB at the enlarged spindle and with cytoplasmic asters after taxol treatment; it disassembled and distributed into the cytoplasm along with TUBB after nocodazole treatment. Disruption of CLTC function using stealth siRNA caused a decreased first polar body extrusion rate and extensive spindle formation and chromosome congression defects. Taken together, these results show that CLTC plays an important role in spindle assembly and chromosome congression through a microtubule correlation mechanism during mouse oocyte maturation.


2016 ◽  
Author(s):  
Jessica Sanders ◽  
Ethan Bateson ◽  
Yuansong Yu ◽  
Michail Nomikos ◽  
Antony Lai ◽  
...  

2014 ◽  
Author(s):  
Xing Duan ◽  
Zhen-Bo Wang ◽  
Xiang-Shun Cui ◽  
Nam-Hyung Kim ◽  
Shao-Chen Sun

Cell Division ◽  
2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Ming-Hong Sun ◽  
Lin-Lin Hu ◽  
Chao-Ying Zhao ◽  
Xiang Lu ◽  
Yan-Ping Ren ◽  
...  

Abstract Background Ral family is a member of Ras-like GTPase superfamily, which includes RalA and RalB. RalA/B play important roles in many cell biological functions, including cytoskeleton dynamics, cell division, membrane transport, gene expression and signal transduction. However, whether RalA/B involve into the mammalian oocyte meiosis is still unclear. This study aimed to explore the roles of RalA/B during mouse oocyte maturation. Results Our results showed that RalA/B expressed at all stages of oocyte maturation, and they were enriched at the spindle periphery area after meiosis resumption. The injection of RalA/B siRNAs into the oocytes significantly disturbed the polar body extrusion, indicating the essential roles of RalA/B for oocyte maturation. We observed that in the RalA/B knockdown oocytes the actin filament fluorescence intensity was significantly increased at the both cortex and cytoplasm, and the chromosomes were failed to locate near the cortex, indicating that RalA/B regulate actin dynamics for spindle migration in mouse oocytes. Moreover, we also found that the Golgi apparatus distribution at the spindle periphery was disturbed after RalA/B depletion. Conclusions In summary, our results indicated that RalA/B affect actin dynamics for chromosome positioning and Golgi apparatus distribution in mouse oocytes.


PLoS ONE ◽  
2015 ◽  
Vol 10 (2) ◽  
pp. e0116783 ◽  
Author(s):  
Petr Solc ◽  
Tomoya S. Kitajima ◽  
Shuhei Yoshida ◽  
Adela Brzakova ◽  
Masako Kaido ◽  
...  

Author(s):  
Chanseob Shim ◽  
Sang Gu Lee ◽  
Woo Keun Song ◽  
Chul Sang Lee ◽  
Kyung-Kwang Lee ◽  
...  

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