Kinesin KIF3A regulates meiotic progression and spindle assembly in oocyte meiosis

• Published in: Cellular and molecular life sciences : CMLS Vol. 81; no. 1; p. 168
• Main Authors: Liu, Jing-Cai, Pan, Zhen-Nan, Ju, Jia-Qian, Zou, Yuan-Jing, Pan, Meng-Hao, Wang, Yue, Wu, Xin, Sun, Shao-Chen
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.12.2024; Springer Nature B.V
• Subjects: Animals; Assembly; Biochemistry; Biological Transport; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cell cycle; Cytoskeleton; Deacetylation; Defects; Depletion; Endoplasmic reticulum; Gametocytes; Golgi apparatus; Histone deacetylase; Intracellular; Kinesin; Kinesins - genetics; Life Sciences; Localization; Maturation; Meiosis; Metaphase; Mice; Microtubules; Molecular motors; mRNA; Oocytes; Original; Original Article; Proteins; Tubulin; Meiosis; Spindle; Kinesin; Oocyte; Cell cycle
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-024-05213-3

Kinesin family member 3A (KIF3A) is a microtubule-oriented motor protein that belongs to the kinesin-2 family for regulating intracellular transport and microtubule movement. In this study, we characterized the critical roles of KIF3A during mouse oocyte meiosis. We found that KIF3A associated with microtubules during meiosis and depletion of KIF3A resulted in oocyte maturation defects. LC–MS data indicated that KIF3A associated with cell cycle regulation, cytoskeleton, mitochondrial function and intracellular transport-related molecules. Depletion of KIF3A activated the spindle assembly checkpoint, leading to metaphase I arrest of the first meiosis. In addition, KIF3A depletion caused aberrant spindle pole organization based on its association with KIFC1 to regulate expression and polar localization of NuMA and γ-tubulin; and KIF3A knockdown also reduced microtubule stability due to the altered microtubule deacetylation by histone deacetylase 6 (HDAC6). Exogenous Kif3a mRNA supplementation rescued the maturation defects caused by KIF3A depletion. Moreover, KIF3A was also essential for the distribution and function of mitochondria, Golgi apparatus and endoplasmic reticulum in oocytes. Conditional knockout of epithelial splicing regulatory protein 1 (ESRP1) disrupted the expression and localization of KIF3A in oocytes. Overall, our results suggest that KIF3A regulates cell cycle progression, spindle assembly and organelle distribution during mouse oocyte meiosis.