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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Analysis of Cryptococcus neoformans Sexual Development Reveals Rewiring of the Pheromone-Response Network by a Change in Transcription Factor Identity
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Analysis of Cryptococcus neoformans Sexual Development Reveals Rewiring of the Pheromone-Response Network by a Change in Transcription Factor Identity

机译:新型隐球菌性发育分析通过转录因子身份的变化揭示了信息素反应网络的重新布线

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摘要

The fundamental mechanisms that control eukaryotic development include extensive regulation at the level of transcription. Gene regulatory networks, composed of transcription factors, their binding sites in DNA, and their target genes, are responsible for executing transcriptional programs. While divergence of these control networks drives species-specific gene expression that contributes to biological diversity, little is known about the mechanisms by which these networks evolve. To investigate how network evolution has occurred in fungi, we used a combination of microarray expression profiling, cis-element identification, and transcription-factor characterization during sexual development of the human fungal pathogen Cryptococcus neoformans. We first defined the major gene expression changes that occur over time throughout sexual development. Through subsequent bioinformatic and molecular genetic analyses, we identified and functionally characterized the C. neoformans pheromone-response element (PRE). We then discovered that transcriptional activation via the PRE requires direct binding of the high-mobility transcription factor Mat2, which we conclude functions as the elusive C. neoformans pheromone-response factor. This function of Mat2 distinguishes the mechanism of regulation through the PRE of C. neoformans from all other fungal systems studied to date and reveals species-specific adaptations of a fungal transcription factor that defies predictions on the basis of sequence alone. Overall, our findings reveal that pheromone-response network rewiring has occurred at the level of transcription factor identity, despite the strong conservation of upstream and downstream components, and serve as a model for how selection pressures act differently on signaling vs. gene regulatory components during eukaryotic evolution.
机译:控制真核生物发育的基本机制包括在转录水平上的广泛调控。由转录因子,它们在DNA中的结合位点和它们的靶基因组成的基因调控网络负责执行转录程序。尽管这些控制网络的差异驱动着有助于生物多样性的物种特异性基因表达,但对这些网络进化的机制知之甚少。为了研究真菌中网络进化的发生方式,我们在人类真菌病原体新隐球菌的有性发育过程中,使用了微阵列表达谱,顺式元件鉴定和转录因子表征的组合。我们首先定义了整个性发育过程中随时间发生的主要基因表达变化。通过随后的生物信息学和分子遗传分析,我们确定了新孢子虫信息素反应元件(PRE)并对其进行了功能表征。然后,我们发现通过PRE进行转录激活需要高迁移率转录因子Mat2的直接结合,而我们得出的结论是,它起着难以捉摸的新孢梭菌信息素反应因子的作用。 Mat2的这一功能通过迄今为止新研究的所有其他真菌系统,将新孢梭菌的PRE调节机制区分开来,并揭示了真菌转录因子的物种特异性适应性,该适应性不符合仅基于序列的预测。总体而言,我们的研究结果表明,尽管上游和下游成分的保守性很强,但信息素反应网络的重新连接发生在转录因子同一性的水平,并且可以作为选择压力如何在信号转导和基因调控成分之间发生不同作用的模型真核进化。

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