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转录组分析 5-氮杂胞苷对黄曲霉菌的响应。

Transcriptomic profiling of Aspergillus flavus in response to 5-azacytidine.

机构信息

MOE Key Laboratory of Aquatic Product Safety, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, China.

出版信息

Fungal Genet Biol. 2013 Jul;56:78-86. doi: 10.1016/j.fgb.2013.04.007. Epub 2013 May 1.

Abstract

Aspergillus flavus is a common saprophyte and opportunistic pathogen producing aflatoxin (AF) and many other secondary metabolites. 5-Azacytidine (5-AC), a derivative of the nucleoside cytidine, is widely used for studies in epigenetics and cancer biology as an inactivator of DNA methyltransferase and is also used for studying secondary metabolism in fungi. Our previous studies showed that 5-AC affects development and inhibits AF production in A. flavus, and that A. flavus lacks DNA methylation. In this study, an RNA-Seq approach was applied to explore the mechanism of 5-AC's effect on A. flavus. We identified 240 significantly differentially expressed (Q-value<0.05) genes after 5-AC treatment, including two backbone genes respectively in secondary metabolite clusters #27 and #35. These two clusters are involved in development or survival of sclerotia. GO functional enrichment analysis showed that these significantly differentially expressed genes were mainly involved in catalytic activity and proteolytic functions. The expressed transcripts of most genes in the AF biosynthetic gene cluster in A. flavus showed no significant changes after treatment with 5-AC and were expressed at low levels, and the transcription regulator genes aflR and aflS in this cluster did not show differential expression relative to the sample without 5-AC treatment. We found that the veA gene, which encodes protein bridges VelB and LaeA, decreased profoundly the expressed transcripts, and brlA, which encodes an early regulator of development, increased its transcripts in A. flavus after 5-AC treatment. Our data support a model whereby 5-AC affects development through increasing the expression of brlA by depressing the expression of veA and AF production through suppressing veA expression and dysregulating carboxypeptidase activity, which then prevents the aflatoxisomes (vesicles) from performing their normal function in AF formation. Furthermore, the suppressed veA expression weakens or even interrupts the connection between VelB and LaeA, leading to dysregulation of the expression pattern of genes involved in development and secondary metabolism in A. flavus. The RNA-seq data presented in this work were also served to improve the annotation of the A. flavus genome. This work provides a comprehensive view of the transcriptome of A. flavus responsive to 5-AC and supports the conclusion that fungal development and secondary metabolism are co-regulated.

摘要

黄曲霉是一种常见的腐生菌和机会致病菌,能产生黄曲霉毒素(AF)和许多其他次级代谢产物。5-氮杂胞苷(5-AC)是胞苷核苷的衍生物,作为 DNA 甲基转移酶的失活剂,广泛用于表观遗传学和癌症生物学的研究,也用于研究真菌中的次级代谢。我们之前的研究表明,5-AC 影响黄曲霉的发育并抑制 AF 的产生,并且黄曲霉缺乏 DNA 甲基化。在这项研究中,我们应用 RNA-Seq 方法来探索 5-AC 对黄曲霉影响的机制。我们发现,5-AC 处理后有 240 个基因的表达显著差异(Q 值<0.05),包括次级代谢物簇#27 和#35 中的两个骨干基因。这两个簇与菌核的发育或存活有关。GO 功能富集分析表明,这些差异表达的基因主要参与催化活性和蛋白水解功能。黄曲霉中 AF 生物合成基因簇的大多数基因的转录本在 5-AC 处理后没有显著变化,并且表达水平较低,并且该簇中的转录调节基因 aflR 和 aflS 与无 5-AC 处理的样本相比没有差异表达。我们发现,编码 VelB 和 LaeA 蛋白桥接物的 veA 基因在 5-AC 处理后,其转录本显著降低,而编码早期发育调节剂的 brlA 基因则增加。我们的数据支持这样一种模型,即 5-AC 通过抑制 veA 的表达来影响发育和 AF 的产生,通过抑制 veA 的表达和调节羧肽酶活性来阻止液泡体(小泡)在 AF 形成中发挥正常功能,从而影响发育。此外,抑制 veA 的表达会削弱甚至中断 VelB 和 LaeA 之间的连接,导致黄曲霉中参与发育和次级代谢的基因的表达模式失调。本工作中提供的 RNA-seq 数据也用于改进黄曲霉基因组的注释。这项工作提供了一个全面的黄曲霉转录组图谱,对 5-AC 响应,并支持真菌发育和次级代谢共同调控的结论。

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