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有丝分裂原活化蛋白激酶级联反应在哺乳动物卵母细胞成熟和受精过程中的作用。

Involvement of mitogen-activated protein kinase cascade during oocyte maturation and fertilization in mammals.

作者信息

Fan Heng-Yu, Sun Qing-Yuan

机构信息

State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100080, P. R. China.

出版信息

Biol Reprod. 2004 Mar;70(3):535-47. doi: 10.1095/biolreprod.103.022830. Epub 2003 Nov 12.

Abstract

Mitogen-activated protein kinase (MAPK) is a family of Ser/Thr protein kinases that are widely distributed in eukaryotic cells. Studies in the last decade revealed that MAPK cascade plays pivotal roles in regulating the meiotic cell cycle progression of oocytes. In mammalian species, activation of MAPK in cumulus cells is necessary for gonadotropin-induced meiotic resumption of oocytes, while MAPK activation is not required for spontaneous meiotic resumption. After germinal vesicle breakdown (GVBD), MAPK is involved in the regulation of microtubule organization and meiotic spindle assembly. The activation of this kinase is essential for the maintenance of metaphase II arrest, while its inactivation is a prerequisite for pronuclear formation after fertilization or parthenogenetic activation. MAPK cascade interacts extensively with other protein kinases such as maturation-promoting factor, protein kinase A, protein kinase C, and calmodulin-dependent protein kinase II, as well as with protein phosphatases in oocyte meiotic cell cycle regulation. The cross talk between MAPK cascade and other protein kinases is discussed. The review also addresses unsolved problems and discusses future directions.

摘要

丝裂原活化蛋白激酶(MAPK)是一类丝氨酸/苏氨酸蛋白激酶家族,广泛分布于真核细胞中。过去十年的研究表明,MAPK级联在调控卵母细胞减数分裂细胞周期进程中起关键作用。在哺乳动物中,卵丘细胞中MAPK的激活是促性腺激素诱导卵母细胞减数分裂恢复所必需的,而自发减数分裂恢复则不需要MAPK激活。在生发泡破裂(GVBD)后,MAPK参与微管组织和减数分裂纺锤体组装的调控。该激酶的激活对于维持中期II阻滞至关重要,而其失活是受精或孤雌激活后原核形成的先决条件。在卵母细胞减数分裂细胞周期调控中,MAPK级联与其他蛋白激酶如促成熟因子、蛋白激酶A、蛋白激酶C和钙调蛋白依赖性蛋白激酶II以及蛋白磷酸酶广泛相互作用。本文讨论了MAPK级联与其他蛋白激酶之间的相互作用。本综述还探讨了未解决的问题并讨论了未来的方向。

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