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Deletion of a Yci1 Domain Protein of Candida albicans Allows Homothallic Mating in MTL Heterozygous Cells

机译:删除白色念珠菌的Yci1结构域蛋白可实现 MTL 杂合子细胞的同型交配。

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ABSTRACT It has been proposed that the ancestral fungus was mating competent and homothallic. However, many mating-competent fungi were initially classified as asexual because their mating capacity was hidden behind layers of regulation. For efficient in vitro mating, the essentially obligate diploid ascomycete pathogen Candida?albicans has to change its mating type locus from heterozygous MTL a /α to homozygous MTL a / a or MTL α/α and then undergo an environmentally controlled epigenetic switch to the mating-competent opaque form. These requirements greatly reduce the potential for C.?albicans mating. Deletion of the Yci1 domain gene OFR1 bypasses the need for C.?albicans cells to change the mating type locus from heterozygous to homozygous prior to switching to the opaque form and mating and allows homothallic mating of MTL heterozygous strains. This bypass is carbon source dependent and does not occur when cells are grown on glucose. Transcriptional profiling of ofr1 mutant cells shows that in addition to regulating cell type and mating circuitry, Ofr1 is needed for proper regulation of histone and chitin biosynthesis gene expression. It appears that OFR1 is a key regulator in C.?albicans and functions in part to maintain the cryptic mating phenotype of the pathogen. IMPORTANCE Candida albicans is a human fungal pathogen with a recently discovered, highly cryptic mating ability. For efficient mating, it has to lose heterozygosity at its mating type locus. Then, MTL homozygous strains can undergo an epigenetic switch to an elongated yeast state, termed the opaque form, and become mating competent. This infrequent two-step process greatly reduces the potential for mating; few strains are MTL homozygous, and the opaque state is unstable at the temperature of the mammalian host. C.?albicans has a complex mechanism for mating that appears designed to ensure that mating is infrequent. Here, we have characterized a new gene, opaque-formation regulator 1 ( OFR1 ). Deleting the OFR1 gene allows MTL a /α strains to mate efficiently with either mating type or even mate homothallically. It is possible that downregulating OFR1 in the host environment could allow mating in C.?albicans by a route that does not involve MTL homozygosis.
机译:摘要有人提出祖传真菌是交配的和同系的。但是,许多具有交配能力的真菌最初被分类为无性真菌,因为它们的交配能力被隐藏在调控层的后面。为了有效地进行体外交配,基本上专性的二倍体子囊菌病原体假丝酵母念珠菌必须将其交配型位点从杂合MTL a /α变为纯合MTL a / a或MTLα/α,然后进行环境控制的表观遗传转换为交配-胜任的不透明形式。这些要求大大降低了白色念珠菌交配的可能性。 Yci1域基因OFR1的删除绕开了白色念珠菌细胞在切换到不透明形式和交配之前将交配型基因座从杂合子改变为纯合子的需要,并允许MTL杂合子菌株的纯合子交配。这种旁路是依赖碳源的,当细胞在葡萄糖上生长时不会发生这种旁路。 Ofr1突变细胞的转录谱分析表明,除了调节细胞类型和交配途径外,Ofr1还需要适当调节组蛋白和甲壳质生物合成基因的表达。看来,OFR1是白色念珠菌的关键调节因子,部分功能是维持病原体的隐性交配表型。重要信息白色念珠菌是一种人类真菌病原体,具有最近发现的高度隐秘的交配能力。为了有效交配,它必须在其交配型位点失去杂合性。然后,MTL纯合菌株可以经历表观遗传转换为伸长的酵母状态(称为不透明形式),并具有交配能力。这种不常见的两步过程大大降低了交配的可能性。 MTL纯合的菌株很少,并且不透明状态在哺乳动物宿主的温度下不稳定。白色念珠菌具有复杂的交配机制,这种机制似乎旨在确保不频繁交配。在这里,我们表征了一个新基因,不透明形成调节子1(OFR1)。删除OFR1基因可使MTL a /α菌株与交配类型有效地交配,甚至与同型交配。在宿主环境中下调OFR1可能允许白色念珠菌通过不涉及MTL纯合的途径交配。

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