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Degradation of Ndd1 by APC/C-Cdh1 generates a feed forward loop that times mitotic protein accumulation

机译:APC / C-Cdh1对Ndd1的降解会产生前馈环,从而使有丝分裂蛋白积累计时

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摘要

Ndd1 activates the Mcm1-Fkh2 transcription factor to transcribe mitotic regulators. The anaphase-promoting complex/cyclosome activated by Cdh1 (APC/C-Cdh1) mediates the degradation of proteins throughout G1. Here we show that the APC/C-Cdh1 ubiquitinates Ndd1 and mediates its degradation, and that APC/C-Cdh1 activity suppresses accumulation of Ndd1 targets. We confirm putative Ndd1 targets and identify novel ones, many of them APC/C-Cdh1 substrates. The APC/C-Cdh1 thus regulates these proteins in a dual manner-both pre-transcriptionally and post-translationally, forming a multi-layered feedforward loop (FFL). We predict by mathematical modelling and verify experimentally that this FFL introduces a lag between APC/C-Cdh1 inactivation at the end of G1 and accumulation of genes transcribed by Ndd1 in G2. This regulation generates two classes of APC/C-Cdh1 substrates, early ones that accumulate in S and late ones that accumulate in G2. Our results show how the dual state APC/C-Cdh1 activity is converted into multiple outputs by interactions between its substrates.
机译:Ndd1激活Mcm1-Fkh2转录因子以转录有丝分裂调节剂。 Cdh1(APC / C-Cdh1)激活的后期促进复合物/环体介导了整个G1蛋白质的降解。在这里,我们显示APC / C-Cdh1泛素化Ndd1并介导其降解,并且APC / C-Cdh1活性抑制Ndd1目标的积累。我们确认推定的Ndd1靶标并鉴定新颖的靶标,其中许多是APC / C-Cdh1底物。因此,APC / C-Cdh1在转录前和翻译后以双重方式调节这些蛋白质,从而形成多层前馈环(FFL)。我们通过数学建模进行预测并通过实验验证,该FFL引入了G1末端APC / C-Cdh1失活与G2中Ndd1转录的基因积累之间的滞后。该法规产生两类APC / C-Cdh1底物,早期的底物积累在S中,晚期的底物积累在G2中。我们的结果表明,双态APC / C-Cdh1活性如何通过其底物之间的相互作用转化为多个输出。

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