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在非洲爪蟾卵提取物的细胞凋亡过程中,Geminin被caspase-3切割。

Geminin is cleaved by caspase-3 during apoptosis in Xenopus egg extracts.

作者信息

Auziol Camille, Méchali Marcel, Maiorano Domenico

机构信息

Institute of Human Genetics, CNRS-UPR14142, Montpellier, France.

出版信息

Biochem Biophys Res Commun. 2007 Sep 21;361(2):276-80. doi: 10.1016/j.bbrc.2007.06.117. Epub 2007 Jul 2.

Abstract

Geminin is an important cell cycle regulator having a dual role in cell proliferation and differentiation. During proliferation, Geminin controls DNA synthesis by interacting with the licensing factor Cdt1 and interferes with the onset of differentiation by inhibiting the activity of transcription factors such as Hox and Six3. During early development Geminin also functions as neural inducer. Thus differential interaction of Geminin with Cdt1 or development-specific transcription factors influence the balance between proliferation and differentiation. Here, we report an additional feature of Geminin showing that it is a novel substrate of caspase-3 during apoptosis in in vitro Xenopus egg extracts. We also show that cleavage of Geminin occurs both in solution and on chromatin with distinct kinetics. In addition we show that cleavage of Geminin by caspase-3 is not relevant to its function as regulator of DNA synthesis, suggesting that its cleavage may be relevant to its role in differentiation.

摘要

Geminin是一种重要的细胞周期调节因子,在细胞增殖和分化中具有双重作用。在增殖过程中,Geminin通过与许可因子Cdt1相互作用来控制DNA合成,并通过抑制Hox和Six3等转录因子的活性来干扰分化的开始。在早期发育过程中,Geminin还作为神经诱导因子发挥作用。因此,Geminin与Cdt1或发育特异性转录因子的差异相互作用影响了增殖和分化之间的平衡。在这里,我们报道了Geminin的另一个特性,表明它是体外非洲爪蟾卵提取物凋亡过程中caspase-3的一种新型底物。我们还表明,Geminin的切割在溶液和染色质上均以不同的动力学发生。此外,我们表明caspase-3对Geminin的切割与其作为DNA合成调节因子的功能无关,这表明其切割可能与其在分化中的作用有关。

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