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Target hub proteins serve as master regulators of development in yeast.

机译:靶标毂蛋白充当酵母中发育的主要调节剂。

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摘要

To understand the organization of the transcriptional networks that govern cell differentiation, we have investigated the transcriptional circuitry controlling pseudohyphal development in Saccharomyces cerevisiae. The binding targets of Ste12, Tec1, Sok2, Phd1, Mga1, and Flo8 were globally mapped across the yeast genome. The factors and their targets form a complex binding network, containing patterns characteristic of autoregulation, feedback and feed-forward loops, and cross-talk. Combinatorial binding to intergenic regions was commonly observed, which allowed for the identification of a novel binding association between Mga1 and Flo8, in which Mga1 requires Flo8 for binding to promoter regions. Further analysis of the network showed that the promoters of MGA1 and PHD1 were bound by all of the factors used in this study, identifying them as key target hubs. Overexpression of either of these two proteins specifically induced pseudohyphal growth under noninducing conditions, highlighting them as masterregulators of the system. Our results indicate that target hubs can serve as master regulators whose activity is sufficient for the induction of complex developmental responses and therefore represent important regulatory nodes in biological networks.
机译:为了了解控制细胞分化的转录网络的组织,我们研究了控制啤酒酵母假菌丝发育的转录电路。 Ste12,Tec1,Sok2,Phd1,Mga1和Flo8的结合靶标在整个酵母基因组中进行了全局定位。这些因素及其目标形成一个复杂的绑定网络,其中包含自动调节,反馈和前馈环路以及串扰的特征模式。通常观察到与基因间区域的组合结合,这允许鉴定Mga1与Flo8之间的新型结合缔合,其中Mga1需要Flo8与启动子区域结合。对网络的进一步分析表明,MGA1和PHD1的启动子受到本研究中使用的所有因素的束缚,将其确定为关键的靶点中心。在非诱导条件下,这两种蛋白质中的任一种的过表达都特异性地诱导假菌丝的生长,从而突出了它们作为系统的主调节剂。我们的结果表明,目标枢纽可以充当主调节器,其活动足以诱导复杂的发育反应,因此代表了生物网络中的重要调节节点。

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