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海鞘卵母细胞减数分裂过程中精子触发的钙振荡首先暂停、重新启动,然后停止:与细胞周期激酶活性的相关性。

Sperm-triggered calcium oscillations during meiosis in ascidian oocytes first pause, restart, then stop: correlations with cell cycle kinase activity.

作者信息

McDougall A, Levasseur M

机构信息

Department of Physiological Sciences, The Medical School, University of Newcastle, Framlington Place, Newcastle upon Tyne NE2 4HH, UK. a.

出版信息

Development. 1998 Nov;125(22):4451-9. doi: 10.1242/dev.125.22.4451.

Abstract

We have investigated the relationship between the sperm-triggered Ca2+ oscillations and the activities of two cell cycle kinases (MPF activity and MAP kinase activity) at fertilisation of Ascidiella aspersa oocytes. Maturation Promoting Factor (MPF) activity is elevated in the metaphase I (MI)-arrested unfertilised oocyte (as measured by phosphorylation of exogenous histone H1) and falls 5 minutes after fertilisation to remain at low levels for 5 minutes. The first polar body (pb1) is extruded when the MPF activity is low. The MPF activity is elevated again 15 minutes after fertilisation and finally becomes inactivated 25 minutes after fertilisation when the pb2 is extruded. MAP kinase activity increases from an initially elevated level to reach maximal activity 10 minutes after fertilisation and subsequently falls to reach low levels 25 minutes after fertilisation. Sperm trigger a series of Ca2+ oscillations that pause for 5 minutes while only the MPF activity is low and are present when both MPF and MAP kinase activity are elevated. We next attempted to determine whether the second phase of calcium oscillations is required to reactivate the MPF activity that precedes extrusion of the second polar body. To do this, we triggered a monotonic Ca2+ signal. This leads to the inactivation of MPF followed by MPF reactivation. The MPF activity then remains elevated for an extended period of time. During this period, the chromatin remains condensed and a metaphase II (MII) spindle forms. Fertilisation of these MII oocytes triggers extrusion of pb2 in 7 minutes. Interestingly, the second phase of Ca2+ oscillations is completely absent when MII oocytes are fertilised. Thus, in both MI and MII oocytes, the sperm-triggered Ca2+ oscillations follow the MPF activity. Finally we discuss our finding that the Ca2+ release system remains sensitive during the metaphase-like state (including the period when the Ca2+ oscillations pause).

摘要

我们研究了精子触发的Ca2+振荡与海鞘卵母细胞受精时两种细胞周期激酶活性(MPF活性和MAP激酶活性)之间的关系。成熟促进因子(MPF)活性在处于中期I(MI)阻滞的未受精卵母细胞中升高(通过外源组蛋白H1的磷酸化来测量),受精后5分钟下降,并在5分钟内保持在低水平。当MPF活性较低时,第一极体(pb1)被排出。受精后15分钟,MPF活性再次升高,最终在受精后25分钟pb2排出时失活。MAP激酶活性从最初升高的水平开始增加,在受精后10分钟达到最大活性,随后在受精后25分钟下降至低水平。精子触发一系列Ca2+振荡,在仅MPF活性较低时暂停5分钟,而当MPF和MAP激酶活性都升高时则会出现。接下来,我们试图确定钙振荡的第二阶段是否是重新激活第二极体排出之前的MPF活性所必需的。为此,我们触发了一个单调的Ca2+信号。这导致MPF失活,随后MPF重新激活。然后MPF活性在较长一段时间内保持升高。在此期间,染色质保持浓缩状态,中期II(MII)纺锤体形成。这些MII卵母细胞受精后7分钟触发pb2排出。有趣的是,MII卵母细胞受精时完全没有Ca2+振荡的第二阶段。因此,在MI和MII卵母细胞中,精子触发的Ca2+振荡都跟随MPF活性。最后,我们讨论了我们的发现,即Ca2+释放系统在中期样状态期间(包括Ca2+振荡暂停的时期)仍然敏感。

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