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在新生隐球菌中,毒力的表观遗传调控和核糖体蛋白基因的转录涉及 YEATS 家族蛋白。

Epigenetic regulation of virulence and the transcription of ribosomal protein genes involves a YEATS family protein in Cryptococcus deneoformans.

机构信息

Beijing Key Laboratory of Genetic Engineering Drug and Biotechnology, Institute of Biochemistry and Molecular Biology, College of Life Sciences, Beijing Normal University (CLS-BNU), Beijing 100875, PR China.

出版信息

FEMS Yeast Res. 2021 Mar 4;21(1). doi: 10.1093/femsyr/foab001.

DOI:10.1093/femsyr/foab001
PMID:33440003
Abstract

Epigenetic marks or post-translational modifications on histones have important regulatory roles in gene expression in eukaryotic organisms. The epigenetic regulation of gene expression in the pathogenic yeast Cryptococcus deneoformans remains largely undetermined. The YEATS domain proteins are readers of crotonylated lysine residues in histones. Here, we reported the identification of a single-copy gene putatively coding for a YEATS domain protein (Yst1) in C. deneoformans. To define its function, we created a mutant strain, yst1Δ, using CRISPR-Cas9 editing. yst1Δ exhibited defects in phenotype, for instance, it was hypersensitive to osmotic stress in the presence of 1.3 M NaCl or KCl. Furthermore, it was hypersensitive to 1% Congo red, suggesting defects in the cell wall. Interestingly, RNA-seq data revealed that Yst1p was critical for the expression of genes encoding the ribosomal proteins, that is, most were expressed with significantly lower levels of mRNA in yst1Δ than in the wild-type strain. The mutant strain was hypersensitive to low temperature and anti-ribosomal drugs, which we putatively attribute to the impairment in ribosomal function. In addition, the yst1Δ strain was less virulent to Galleria mellonella. These results generally suggest that Yst1, as a histone modification reader, might be a key coordinator of the transcriptome of this human pathogen. Yst1 could be a potential target for novel antifungal drugs, which might lead to significant developments in the clinical treatment of cryptococcosis.

摘要

组蛋白上的表观遗传标记或翻译后修饰在真核生物的基因表达中具有重要的调控作用。致病性酵母新生隐球菌中基因表达的表观遗传调控在很大程度上仍未确定。YEATS 结构域蛋白是组蛋白中丙二酰化赖氨酸残基的阅读器。在这里,我们报道了在新生隐球菌中鉴定出一个单一拷贝的基因,该基因可能编码 YEATS 结构域蛋白(Yst1)。为了定义其功能,我们使用 CRISPR-Cas9 编辑创建了一个突变株 yst1Δ。yst1Δ 在表型上表现出缺陷,例如,在存在 1.3 M NaCl 或 KCl 的情况下,它对渗透压胁迫敏感。此外,它对 1%刚果红敏感,表明细胞壁有缺陷。有趣的是,RNA-seq 数据显示 Yst1p 对编码核糖体蛋白的基因的表达至关重要,即在 yst1Δ 中的 mRNA 表达水平明显低于野生型菌株。突变株对低温和抗核糖体药物敏感,我们推测这归因于核糖体功能的损伤。此外,yst1Δ 菌株对金龟子幼虫的毒力降低。这些结果总体表明,作为一种组蛋白修饰阅读器,Yst1 可能是这种人类病原体转录组的关键协调者。Yst1 可以成为新型抗真菌药物的潜在靶点,这可能会在隐球菌病的临床治疗方面带来重大进展。

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