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全面解析与白念珠菌形态发生和毒力相关的两种热休克因子型转录调控因子的功能特征。

A comprehensive functional portrait of two heat shock factor-type transcriptional regulators involved in Candida albicans morphogenesis and virulence.

机构信息

Institut Pasteur, Unité Biologie et Pathogénicité Fongiques, Département Génomes et Génétique, Paris, France.

出版信息

PLoS Pathog. 2013 Aug;9(8):e1003519. doi: 10.1371/journal.ppat.1003519. Epub 2013 Aug 15.

Abstract

Sfl1p and Sfl2p are two homologous heat shock factor-type transcriptional regulators that antagonistically control morphogenesis in Candida albicans, while being required for full pathogenesis and virulence. To understand how Sfl1p and Sfl2p exert their function, we combined genome-wide location and expression analyses to reveal their transcriptional targets in vivo together with the associated changes of the C. albicans transcriptome. We show that Sfl1p and Sfl2p bind to the promoter of at least 113 common targets through divergent binding motifs and modulate directly the expression of key transcriptional regulators of C. albicans morphogenesis and/or virulence. Surprisingly, we found that Sfl2p additionally binds to the promoter of 75 specific targets, including a high proportion of hyphal-specific genes (HSGs; HWP1, HYR1, ECE1, others), revealing a direct link between Sfl2p and hyphal development. Data mining pointed to a regulatory network in which Sfl1p and Sfl2p act as both transcriptional activators and repressors. Sfl1p directly represses the expression of positive regulators of hyphal growth (BRG1, UME6, TEC1, SFL2), while upregulating both yeast form-associated genes (RME1, RHD1, YWP1) and repressors of morphogenesis (SSN6, NRG1). On the other hand, Sfl2p directly upregulates HSGs and activators of hyphal growth (UME6, TEC1), while downregulating yeast form-associated genes and repressors of morphogenesis (NRG1, RFG1, SFL1). Using genetic interaction analyses, we provide further evidences that Sfl1p and Sfl2p antagonistically control C. albicans morphogenesis through direct modulation of the expression of important regulators of hyphal growth. Bioinformatic analyses suggest that binding of Sfl1p and Sfl2p to their targets occurs with the co-binding of Efg1p and/or Ndt80p. We show, indeed, that Sfl1p and Sfl2p targets are bound by Efg1p and that both Sfl1p and Sfl2p associate in vivo with Efg1p. Taken together, our data suggest that Sfl1p and Sfl2p act as central "switch on/off" proteins to coordinate the regulation of C. albicans morphogenesis.

摘要

Sfl1p 和 Sfl2p 是两种同源的热休克因子型转录调节因子,它们在白念珠菌中拮抗地控制形态发生,同时也是完全发病机制和毒力所必需的。为了了解 Sfl1p 和 Sfl2p 如何发挥作用,我们结合全基因组定位和表达分析,揭示了它们在体内的转录靶标以及白念珠菌转录组的相关变化。我们表明,Sfl1p 和 Sfl2p 通过不同的结合基序结合到至少 113 个共同靶标的启动子上,并直接调节白念珠菌形态发生和/或毒力的关键转录调节因子的表达。令人惊讶的是,我们发现 Sfl2p 还结合到 75 个特定靶标的启动子上,包括大量菌丝特异性基因(HSGs;HWP1、HYR1、ECE1 等),这表明 Sfl2p 与菌丝发育之间存在直接联系。数据挖掘指向一个调节网络,其中 Sfl1p 和 Sfl2p 既作为转录激活因子又作为转录抑制因子发挥作用。Sfl1p 直接抑制菌丝生长的正调节因子(BRG1、UME6、TEC1、SFL2)的表达,同时上调酵母形态相关基因(RME1、RHD1、YWP1)和形态发生抑制剂(SSN6、NRG1)。另一方面,Sfl2p 直接上调 HSGs 和菌丝生长的激活因子(UME6、TEC1),同时下调酵母形态相关基因和形态发生抑制剂(NRG1、RFG1、SFL1)。通过遗传相互作用分析,我们进一步提供证据表明,Sfl1p 和 Sfl2p 通过直接调节菌丝生长的重要调节因子的表达来拮抗地控制白念珠菌的形态发生。生物信息学分析表明,Sfl1p 和 Sfl2p 与其靶标的结合伴随着 Efg1p 和/或 Ndt80p 的共同结合。我们确实表明,Sfl1p 和 Sfl2p 的靶标被 Efg1p 结合,并且 Sfl1p 和 Sfl2p 都在体内与 Efg1p 相关联。总之,我们的数据表明,Sfl1p 和 Sfl2p 作为中央“开/关”蛋白,协调白念珠菌形态发生的调节。

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