Abf1 负向调控 EPA1 的表达并影响白色念珠菌的粘附性。

Grecia Hernández-Hernández, Laura A Vera-Salazar, Guadalupe Gutiérrez-Escobedo, Nicolás Gómez-Hernández, Osney Leiva-Peláez, Alejandro De Las Peñas, Irene Castaño
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引用次数: 0

摘要

导言。粘附性是一种主要的光滑念珠菌毒力特征,在许多菌株中,粘附性取决于 EPA(上皮粘附素)基因,该基因赋予光滑念珠菌粘附宿主上皮细胞和内皮细胞的能力。EPA 基因通常存在于亚基因组区域,因此会受到亚基因组沉默的影响。在草履虫中,亚群沉默取决于不同的蛋白复合物,如沉默信息调节器和yKu复合物,以及其他蛋白,如抑制器/激活蛋白1(Rap1)和Abf1。在编码主要粘附蛋白 Epa1 的 EPA1 基因座上,我们先前发现了至少两个顺式作用元件,即原丝器 Sil2126 和负元件,它们有助于沉默从端粒传播到次端粒区。Abf1与端粒E-R的EPA1和其他区域的调节区域结合,从而负向调节EPA1的转录。确定 Abf1 和 Rap1 沉默蛋白是否与之前确定的 E 染色体右端粒(E-R 次端粒区)上的顺式作用元件结合,从而导致 EPA1 转录的负调控,并推断 Abf1 和 Rap1 在 C. glabrata 中的识别位点。我们利用染色质免疫沉淀(ChIP)和定量 PCR 方法确定了 EPA1 和 EPA2 之间以及 HYR1 和 EPA1 之间基因间区的 Abf1 和 Rap1 结合位点,并利用突变体确定了 EPA1 启动子区的沉默水平。我们发现 Abf1 主要与 EPA1 启动子区域结合,导致 EPA1 表达的负调控。此外,突变体 abf1-43 的 C 端缺少最后 43 个氨基酸,存在亚群沉默缺陷,与亲本相比,在体外表现出对上皮细胞的超粘附性,这表明 EPA1 受到了去抑制。我们还利用 ChIP 检测数据确定了 C. glabrata 中 Abf1 和 Rap1 的主题结合序列。这些数据共同表明,Abf1 负向调节 EPA1 的表达,从而降低了 C. glabrata 对上皮细胞的粘附力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abf1 negatively regulates the expression of EPA1 and affects adhesion in Candida glabrata.

Introduction. Adherence is a major virulence trait in Candida glabrata that, in many strains, depends on the EPA (epithelial adhesin) genes, which confer the ability to adhere to epithelial and endothelial cells of the host. The EPA genes are generally found at subtelomeric regions, which makes them subject to subtelomeric silencing. In C. glabrata, subtelomeric silencing depends on different protein complexes, such as silent information regulator and yKu complexes, and other proteins, such as Repressor/activator protein 1 (Rap1) and Abf1. At the EPA1 locus, which encodes the main adhesin Epa1, we previously found at least two cis-acting elements, the protosilencer Sil2126 and the negative element, that contribute to the propagation of silencing from the telomere to the subtelomeric region.Hypothesis. Abf1 binds to the regulatory regions of EPA1 and other regions at the telomere E-R, thereby negatively regulating EPA1 transcription.Aim. To determine whether Abf1 and Rap1 silencing proteins bind to previously identified cis-acting elements on the right telomere of chromosome E (E-R subtelomeric region), resulting in negative regulation of EPA1 transcription and infer Abf1 and Rap1 recognition sites in C. glabrata.Methodology. We used chromatin immunoprecipitation (ChIP) followed by quantitative PCR to determine the binding sites for Abf1 and Rap1 in the intergenic regions between EPA1 and EPA2 and HYR1 and EPA1, and mutants were used to determine the silencing level of the EPA1 promoter region.Results. We found that Abf1 predominantly binds to the EPA1 promoter region, leading to negative regulation of EPA1 expression. Furthermore, the mutant abf1-43, which lacks the last 43 amino acids at its C-terminal end and is defective for subtelomeric silencing, exhibits hyperadherence to epithelial cells in vitro compared to the parental strain, suggesting that EPA1 is derepressed. We also determined the motif-binding sequences for Abf1 and Rap1 in C. glabrata using data from the ChIP assays.Conclusion. Together these data indicate that Abf1 negatively regulates EPA1 expression, leading to decreased adhesion of C. glabrata to epithelial cells.

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