Kim Samin, Nguyen Quoc Bao, Wolyniak Michael J, Frechette Gregory, Lehman Christian R, Fox Brandon K, Sundstrom Paula
Department of Microbiology and Immunology, Microbiology and Molecular Pathogenesis Program, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, United States of America.
Department of Biology, Hampden-Sydney College, Hampden-Sydney, Virginia, United States of America.
PLoS One. 2018 Feb 13;13(2):e0192260. doi: 10.1371/journal.pone.0192260. eCollection 2018.
The mechanisms that fungi use to co-regulate subsets of genes specifically associated with morphogenic states represent a basic unsolved problem in fungal biology. Candida albicans is an important model of fungal differentiation both for rapid interconversion between yeast and hyphal growth forms and for white/opaque switching mechanisms. The Sundstrom lab is interested in mechanisms regulating hypha-specific expression of adhesin genes that are critical for C. albicans hyphal growth phenotypes and pathogenicity. Early studies on hypha-specific genes such as HWP1 and ALS3 reported 5' intergenic regions that are larger than those typically found in an average promoter and are associated with hypha-specific expression. In the case of HWP1, activation and repression involves a 368 bp region, denoted the HWP1 control region (HCR), located 1410 bp upstream of its transcription start site. In previous work we showed that HCR confers developmental regulation to a heterologous ENO1 promoter, indicating that HCR by itself contains sufficient information to couple gene expression to morphology. Here we show that the activation and repression mediated by HCR are localized to distinct HCR regions that are targeted by the transcription factors Nrg1p and Efg1p. The finding that Efg1p mediates both repression via HCR under yeast morphological conditions and activation conditions positions Efg1p as playing a central role in coupling HWP1 expression to morphogenesis through the HCR region. These localization studies revealed that the 120 terminal base pairs of HCR confer Efg1p-dependent repressive activity in addition to the Nrg1p repressive activity mediated by DNA upstream of this subregion. The 120 terminal base pair subregion of HCR also contained an initiation site for an HWP1 transcript that is specific to yeast growth conditions (HCR-Y) and may function in the repression of downstream DNA. The detection of an HWP1 mRNA isoform specific to hyphal growth conditions (HWP1-H) showed that morphology-specific mRNA isoforms occur under both yeast and hyphal growth conditions. Similar results were found at the ALS3 locus. Taken together, these results, suggest that the long 5' intergenic regions upstream of hypha-specific genes function in generating mRNA isoforms that are important for morphology-specific gene expression. Additional complexity in the HWP1 promoter involving HCR-independent activation was discovered by creating a strain lacking HCR that exhibited variable HWP1 expression during hyphal growth conditions. These results show that while HCR is important for ensuring uniform HWP1 expression in cell populations, HCR independent expression also exists. Overall, these results elucidate HCR-dependent mechanisms for coupling HWP1-dependent gene expression to morphology uniformly in cell populations and prompt the hypothesis that mRNA isoforms may play a role in coupling gene expression to morphology in C. albicans.
真菌用于共同调节与形态发生状态特异性相关的基因子集的机制,是真菌生物学中一个基本的未解问题。白色念珠菌是真菌分化的重要模型,它既能在酵母和菌丝生长形式之间快速相互转换,又具有白色/不透明转换机制。桑德斯特伦实验室对调节粘附素基因菌丝特异性表达的机制感兴趣,这些基因对白色念珠菌的菌丝生长表型和致病性至关重要。早期对诸如HWP1和ALS3等菌丝特异性基因的研究报道了5'基因间隔区,其比平均启动子中通常发现的区域更大,并且与菌丝特异性表达相关。就HWP1而言,激活和抑制涉及一个368 bp的区域,称为HWP1控制区(HCR),位于其转录起始位点上游1410 bp处。在先前的工作中,我们表明HCR赋予异源ENO1启动子发育调控能力,这表明HCR自身包含将基因表达与形态学联系起来的足够信息。在这里,我们表明由HCR介导的激活和抑制定位于不同的HCR区域,这些区域是转录因子Nrg1p和Efg1p的作用靶点。Efg1p在酵母形态条件和激活条件下均通过HCR介导抑制和激活这一发现,表明Efg1p在通过HCR区域将HWP1表达与形态发生联系起来方面发挥着核心作用。这些定位研究表明,除了该子区域上游DNA介导的Nrg1p抑制活性外,HCR的120个末端碱基对还赋予Efg1p依赖性抑制活性。HCR的120个末端碱基对子区域还包含一个HWP1转录本的起始位点,该转录本特定于酵母生长条件(HCR-Y),可能在下游DNA的抑制中起作用。对菌丝生长条件特异性的HWP1 mRNA亚型(HWP1-H)的检测表明,形态特异性mRNA亚型在酵母和菌丝生长条件下均会出现。在ALS3基因座也发现了类似的结果。综上所述,这些结果表明,菌丝特异性基因上游的长5'基因间隔区在产生对形态特异性基因表达很重要的mRNA亚型中发挥作用。通过创建一个缺乏HCR的菌株,发现HWP1启动子中涉及不依赖HCR的激活的额外复杂性,该菌株在菌丝生长条件下表现出可变的HWP表达式。这些结果表明,虽然HCR对于确保细胞群体中HWP1表达的均匀性很重要,但不依赖HCR的表达也存在。总体而言,这些结果阐明了在细胞群体中使HWP1依赖性基因表达与形态学均匀联系起来的HCR依赖性机制,并提出了mRNA亚型可能在白色念珠菌中将基因表达与形态学联系起来发挥作用的假设。