Environmentally contingent control of Candida albicans cell wall integrity by transcriptional regulator Cup9.

IF 3.3 3区 生物学 Genetics Pub Date : 2021-07-14 DOI:10.1093/genetics/iyab075
Yuichi Ichikawa, Vincent M Bruno, Carol A Woolford, Hannah Kim, Eunsoo Do, Grace C Brewer, Aaron P Mitchell
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Abstract

The fungal pathogen Candida albicans is surrounded by a cell wall that is the target of caspofungin and other echinocandin antifungals. Candida albicans can grow in several morphological forms, notably budding yeast and hyphae. Yeast and hyphal forms differ in cell wall composition, leading us to hypothesize that there may be distinct genes required for yeast and hyphal responses to caspofungin. Mutants in 27 genes reported previously to be caspofungin hypersensitive under yeast growth conditions were all caspofungin hypersensitive under hyphal growth conditions as well. However, a screen of mutants defective in transcription factor genes revealed that Cup9 is required for normal caspofungin tolerance under hyphal and not yeast growth conditions. In a hyphal-defective efg1Δ/Δ background, Cup9 is still required for normal caspofungin tolerance. This result argues that Cup9 function is related to growth conditions rather than cell morphology. RNA-seq conducted under hyphal growth conditions indicated that 361 genes were up-regulated and 145 genes were down-regulated in response to caspofungin treatment. Both classes of caspofungin-responsive genes were enriched for cell wall-related proteins, as expected for a response to disruption of cell wall integrity and biosynthesis. The cup9Δ/Δ mutant, treated with caspofungin, had reduced RNA levels of 40 caspofungin up-regulated genes, and had increased RNA levels of 8 caspofungin down-regulated genes, an indication that Cup9 has a narrow rather than global role in the cell wall integrity response. Five Cup9-activated surface-protein genes have roles in cell wall integrity, based on mutant analysis published previously (PGA31 and IFF11) or shown here (ORF19.3499, ORF19.851, or PGA28), and therefore may explain the hypersensitivity of the cup9Δ/Δmutant to caspofungin. Our findings define Cup9 as a new determinant of caspofungin susceptibility.

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转录调节因子 Cup9 对白色念珠菌细胞壁完整性的环境控制。
真菌病原体白色念珠菌有一层细胞壁,是卡泊芬净和其他棘白菌素类抗真菌药的靶标。白色念珠菌可以多种形态生长,主要是出芽酵母和菌丝。酵母和菌丝的细胞壁组成不同,因此我们推测酵母和菌丝对卡泊芬净的反应可能需要不同的基因。之前报道的在酵母生长条件下对环孢菌素不敏感的 27 个基因的突变体,在菌丝生长条件下也对环孢菌素不敏感。然而,对转录因子基因缺陷突变体的筛选发现,Cup9 是在芽孢生长条件下而不是在酵母生长条件下正常耐受卡泊芬净所必需的。在缺损的efg1Δ/Δ背景中,Cup9仍然是正常耐受caspofungin所必需的。这一结果证明 Cup9 的功能与生长条件而非细胞形态有关。在菌丝生长条件下进行的RNA-seq分析表明,361个基因上调,145个基因下调。这两类caspofungin反应基因都富含细胞壁相关蛋白,这是对破坏细胞壁完整性和生物合成的反应所预期的。经caspofungin处理的cup9Δ/Δ突变体的40个caspofungin上调基因的RNA水平降低,而8个caspofungin下调基因的RNA水平升高,这表明Cup9在细胞壁完整性反应中的作用是狭义的,而不是全局性的。根据以前发表的突变体分析(PGA31 和 IFF11)或这里显示的突变体分析(ORF19.3499、ORF19.851 或 PGA28),有五个 Cup9 激活的表面蛋白基因在细胞壁完整性中发挥作用,因此可以解释 cup9Δ/Δ 突变体对 caspofungin 的超敏反应。我们的发现将 Cup9 定义为对卡泊芬净敏感的新决定因素。
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来源期刊
Genetics
Genetics 生物-遗传学
CiteScore
6.20
自引率
6.10%
发文量
177
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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