Department of Biochemistry, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.
Mol Cell. 2013 Nov 7;52(3):325-39. doi: 10.1016/j.molcel.2013.08.043. Epub 2013 Oct 3.
Active metabolism regulates oocyte cell death via calcium/calmodulin-dependent protein kinase II (CaMKII)-mediated phosphorylation of caspase-2, but the link between metabolic activity and CaMKII is poorly understood. Here we identify coenzyme A (CoA) as the key metabolic signal that inhibits Xenopus laevis oocyte apoptosis by directly activating CaMKII. We found that CoA directly binds to the CaMKII regulatory domain in the absence of Ca(2+) to activate CaMKII in a calmodulin-dependent manner. Furthermore, we show that CoA inhibits apoptosis not only in X. laevis oocytes but also in Murine oocytes. These findings uncover a direct mechanism of CaMKII regulation by metabolism and further highlight the importance of metabolism in preserving oocyte viability.
活性代谢通过钙/钙调蛋白依赖性蛋白激酶 II(CaMKII)介导的半胱天冬酶-2磷酸化来调节卵母细胞细胞死亡,但是代谢活性与 CaMKII 之间的联系尚不清楚。在这里,我们确定辅酶 A(CoA)是关键的代谢信号,它通过直接激活 CaMKII 来抑制非洲爪蟾卵母细胞凋亡。我们发现 CoA 在没有 Ca(2+)的情况下直接与 CaMKII 的调节结构域结合,以钙调蛋白依赖的方式激活 CaMKII。此外,我们还表明 CoA 不仅在非洲爪蟾卵母细胞中,而且在鼠卵母细胞中也能抑制细胞凋亡。这些发现揭示了代谢调节 CaMKII 的直接机制,并进一步强调了代谢在维持卵母细胞活力方面的重要性。