首页> 外文期刊>Genes to cells : >Functional analyses of mouse ASK, an activation subunit for Cdc7 kinase, using conditional ASK knockout ES cells.
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Functional analyses of mouse ASK, an activation subunit for Cdc7 kinase, using conditional ASK knockout ES cells.

机译:使用条件性ASK敲除ES细胞对小鼠ASK(Cdc7激酶的激活亚基)进行功能分析。

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摘要

ASK (activator of S phase kinase) is an activation subunit for mammalian Cdc7 kinase. We have generated mutant ES cell lines in which ASK can be conditionally inactivated. Upon loss of the ASK genes, the mutant ES cells rapidly cease cell growth. In keeping with its expected roles in activation of the essential S phase kinase, DNA synthesis is arrested and significant cell death is eventually induced in ASK-deficient cells, demonstrating essential roles of ASK for viability of ES cells. Using these mutant cells, we have set up a system where ASK molecules can be functionally dissected. In keeping with previous results from yeasts, conserved motif-M and motif-C were shown to be essential for in vivo functions of ASK, whereas a long C-terminal tail, found only in ASK-related molecules in higher eukaryotes, is not required. Unexpectedly, the motif-N, related to the BRCT motif and dispensable for viability in yeasts, is essential for the viability of ES cells. Further characterization reveals that motif-N is required for the maximum phosphorylation of MCM in cells, whereas the autophosphorylation activity of Cdc7 is not significantly affected by its loss. These results may suggest that motif-N of ASK may facilitate recruitment of substrates for Cdc7 kinase.
机译:ASK(S期激酶激活剂)是哺乳动物Cdc7激酶的激活亚基。我们已经产生了可以有条件地失活ASK的突变ES细胞系。一旦丢失ASK基因,突变的ES细胞迅速停止细胞生长。与其在必需的S期激酶激活中的预期作用保持一致,DNA合成被停止,并且最终在ASK缺陷细胞中诱导了明显的细胞死亡,这证明了ASK对于ES细胞活力的重要作用。使用这些突变细胞,我们建立了一个可以在功能上解剖ASK分子的系统。与酵母先前的结果一致,保守的基序M和基序C被证明对ASK的体内功能至关重要,而不需要在高级真核生物中仅在ASK相关分子中发现的长C末端尾巴。 。出乎意料的是,与BRCT基序有关并且对于酵母中的生存力而言是可有可无的,基序N对ES细胞的生存力至关重要。进一步的特征表明,基序-N是细胞中MCM的最大磷酸化所必需的,而Cdc7的自磷酸化活性不受其丢失的影响。这些结果可能表明ASK的基序N可以促进Cdc7激酶的底物募集。

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