State Key Laboratory of Crop Stress Biology for Arid Areas and NWAFU-Purdue Joint Research Center, College of Plant Protection, Northwest A&F University, Yangling, Shaanxi, China.
Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States of America.
PLoS Genet. 2020 Nov 2;16(11):e1009185. doi: 10.1371/journal.pgen.1009185. eCollection 2020 Nov.
Histone acetylation, balanced by histone acetyltransferase (HAT) and histone deacetylase (HDAC) complexes, affects dynamic transitions of chromatin structure to regulate transcriptional accessibility. However, little is known about the interplay between HAT and HDAC complexes in Fusarium graminearum, a causal agent of Fusarium Head Blight (FHB) that uniquely contains chromosomal regions enriched for house-keeping or infection-related genes. In this study, we identified the ortholog of the human inhibitor of growth (ING1) gene in F. graminearum (FNG1) and found that it specifically interacts with the FgEsa1 HAT of the NuA4 complex. Deletion of FNG1 led to severe growth defects and blocked conidiation, sexual reproduction, DON production, and plant infection. The fng1 mutant was normal in H3 acetylation but significantly reduced in H4 acetylation. A total of 34 spontaneous suppressors of fng1 with faster growth rate were isolated. Most of them were still defective in sexual reproduction and plant infection. Thirty two of them had mutations in orthologs of yeast RPD3, SIN3, and SDS3, three key components of the yeast Rpd3L HDAC complex. Four mutations in these three genes were verified to suppress the defects of fng1 mutant in growth and H4 acetylation. The rest two suppressor strains had a frameshift or nonsense mutation in a glutamine-rich hypothetical protein that may be a novel component of the FgRpd3 HDAC complex in filamentous fungi. FgRpd3, like Fng1, localized in euchromatin. Deletion of FgRPD3 resulted in severe growth defects and elevated H4 acetylation. In contract, the Fgsds3 deletion mutant had only a minor reduction in growth rate but FgSIN3 appeared to be an essential gene. RNA-seq analysis revealed that 48.1% and 54.2% of the genes with altered expression levels in the fng1 mutant were recovered to normal expression levels in two suppressor strains with mutations in FgRPD3 and FgSDS3, respectively. Taken together, our data showed that Fng1 is important for H4 acetylation as a component of the NuA4 complex and functionally related to the FgRpd3 HDAC complex for transcriptional regulation of genes important for growth, conidiation, sexual reproduction, and plant infection in F. graminearum.
组蛋白乙酰化由组蛋白乙酰转移酶 (HAT) 和组蛋白去乙酰化酶 (HDAC) 复合物平衡,影响染色质结构的动态转变,从而调节转录的可及性。然而,在禾谷镰刀菌(一种独特的包含富含管家或感染相关基因的染色体区域的赤霉病的病原体)中,HAT 和 HDAC 复合物之间的相互作用知之甚少。在本研究中,我们在禾谷镰刀菌中鉴定了人类生长抑制剂 (ING1) 基因的同源物(FNG1),并发现它特异性地与 NuA4 复合物的 FgEsa1 HAT 相互作用。FNG1 的缺失导致严重的生长缺陷,并阻断了分生孢子形成、有性生殖、DON 产生和植物感染。fng1 突变体在 H3 乙酰化方面正常,但 H4 乙酰化显著降低。共分离出 34 个生长速度较快的 fng1 自发抑制子。它们大多数在有性生殖和植物感染方面仍然有缺陷。其中 32 个在酵母 RPD3、SIN3 和 SDS3 的同源物中有突变,这三个是酵母 Rpd3L HDAC 复合物的关键成分。在这三个基因中验证了四个突变可抑制 fng1 突变体在生长和 H4 乙酰化方面的缺陷。其余两个抑制子菌株在一个富含谷氨酰胺的假设蛋白中发生移码或无义突变,该蛋白可能是丝状真菌 FgRpd3 HDAC 复合物的一个新成分。FgRpd3 与 Fng1 一样,定位于常染色质。FgRPD3 的缺失导致严重的生长缺陷和 H4 乙酰化升高。相比之下,Fgsds3 缺失突变体的生长速度仅略有下降,但 FgSIN3 似乎是一个必需基因。RNA-seq 分析显示,在 fng1 突变体中改变表达水平的基因有 48.1%和 54.2%在两个 FgRPD3 和 FgSDS3 突变的抑制子菌株中恢复到正常表达水平。总之,我们的数据表明,Fng1 作为 NuA4 复合物的一个组成部分,对 H4 乙酰化很重要,并且在转录调控对禾谷镰刀菌生长、分生孢子形成、有性生殖和植物感染重要的基因方面,与 FgRpd3 HDAC 复合物功能相关。