Yu Houlin, Yang He, Haridas Sajeet, Hayes Richard D, Lynch Hunter, Andersen Sawyer, Li Gengtan, Martínez-Soto Domingo, Milo-Cochavi Shira, Ayhan Dilay Hazal, Zhang Yong, Grigoriev Igor V, Ma Li-Jun
Department of Biochemistry and Molecular Biology, University of Massachusetts Amherst, Amherst, MA 01003, USA.
Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, University of California Berkeley, Berkeley, CA 94720, USA.
bioRxiv. 2023 Feb 10:2023.02.09.527873. doi: 10.1101/2023.02.09.527873.
The species complex (FOSC) includes both plant and human pathogens that cause devastating plant vascular wilt diseases and threaten public health. Each genome comprises core chromosomes (CCs) for housekeeping functions and accessory chromosomes (ACs) that contribute to host-specific adaptation. This study inspected global transcription factor profiles (TFomes) and their potential roles in coordinating CCs and ACs functions to accomplish host-specific pathogenicity. Remarkably, we found a clear positive correlation between the sizes of TFome and proteome of an organism, and FOSC TFomes are larger due to the acquisition of ACs. Among a total of 48 classified TF families, 14 families involved in transcription/translation regulations and cell cycle controls are highly conserved. Among 30 FOSC expanded families, Zn2-C6 and Znf_C2H2 are most significantly expanded to 671 and 167 genes per family, including well-characterized homologs of Ftf1 (Zn2-C6) and PacC (Znf_C2H2) involved in host-specific interactions. Manual curation of characterized TFs increased the TFome repertoires by 3%, including a disordered protein Ren1. Expression profiles revealed a steady expression of conserved TF families and specific activation of AC TFs. Functional characterization of these TFs could enhance our understanding of transcriptional regulation involved in FOSC cross-kingdom interactions, disentangle species-specific adaptation, and identify targets to combat diverse diseases caused by this group of fungal pathogens.
该物种复合体(FOSC)包括植物和人类病原体,它们会引发毁灭性的植物维管束萎蔫病并威胁公众健康。每个基因组都包含用于维持基本功能的核心染色体(CCs)和有助于宿主特异性适应的辅助染色体(ACs)。本研究检查了全局转录因子谱(TFomes)及其在协调CCs和ACs功能以实现宿主特异性致病性方面的潜在作用。值得注意的是,我们发现生物体的TFome大小与蛋白质组大小之间存在明显的正相关,并且由于获得了ACs,FOSC的TFomes更大。在总共48个分类的TF家族中,14个参与转录/翻译调控和细胞周期控制的家族高度保守。在30个FOSC扩展家族中,Zn2-C6和Znf_C2H2扩展最为显著,每个家族分别达到671个和167个基因,包括参与宿主特异性相互作用的Ftf1(Zn2-C6)和PacC(Znf_C2H2)的特征明确的同源物。对已表征TFs的人工整理使TFome库增加了3%,其中包括一种无序蛋白Ren1。表达谱显示保守TF家族的稳定表达和AC TF的特异性激活。对这些TFs的功能表征可以增强我们对FOSC跨界相互作用中涉及的转录调控的理解,解开物种特异性适应机制,并确定对抗由这组真菌病原体引起的各种疾病的靶点。