Many faces of separase regulation.

SEB experimental biology series Pub Date : 2008-01-01
Andrew J Holland, Stephen S Taylor
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Abstract

In the last decade, yeast genetics has played an instrumental role in identifying conserved components of the machinery that holds sister chromatids together and promotes their separation at anaphase. However, we still lack a molecular understanding which can explain the 'all-or-nothing' nature of sister chromatid separation. A formidable challenge for the future will be to elucidate how multiple layers of control act at both the level of separase and its substrate to regulate the global cleavage of cohesin at anaphase. Such a challenge will benefit from the development of in vivo real-time, high-resolution biomarkers of separase activation and cohesin cleavage. Furthermore, a move towards specifically compromising securin's inhibitory function without affecting the protein's chaperone role is required if we are to understand the true value of other pathways controlling separase activation and cohesin cleavage.

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独立监管的许多方面。
在过去的十年中,酵母遗传学在鉴定将姐妹染色单体保持在一起并促进其后期分离的机制的保守成分方面发挥了重要作用。然而,我们仍然缺乏一个分子的理解,可以解释姐妹染色单体分离的“全有或全无”性质。未来的一个巨大挑战将是阐明分离酶及其底物水平上的多层控制如何调节后期内聚蛋白的全局裂解。这一挑战将受益于分离酶激活和黏结蛋白裂解的体内实时、高分辨率生物标志物的发展。此外,如果我们要了解控制分离酶激活和内聚蛋白切割的其他途径的真正价值,就需要在不影响蛋白质伴侣作用的情况下,明确地损害securin的抑制功能。
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