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刚地弓形虫 F-Box 蛋白 L2 作为一种转录抑制因子调控虫体阶段特异性基因的表达。

The Toxoplasma gondii F-Box Protein L2 Functions as a Repressor of Stage Specific Gene Expression.

机构信息

Department of Microbiology and Immunology, University at Buffalo School of Medicine, Buffalo, New York, United States of America.

Department of Biochemistry & Molecular Biology, Center for Tropical & Emerging Global Diseases, University of Georgia, Athens, Georgia United States of America.

出版信息

PLoS Pathog. 2024 May 30;20(5):e1012269. doi: 10.1371/journal.ppat.1012269. eCollection 2024 May.

Abstract

Toxoplasma gondii is a foodborne pathogen that can cause severe and life-threatening infections in fetuses and immunocompromised patients. Felids are its only definitive hosts, and a wide range of animals, including humans, serve as intermediate hosts. When the transmissible bradyzoite stage is orally ingested by felids, they transform into merozoites that expand asexually, ultimately generating millions of gametes for the parasite sexual cycle. However, bradyzoites in intermediate hosts differentiate exclusively to disease-causing tachyzoites, which rapidly disseminate throughout the host. Though tachyzoites are well-studied, the molecular mechanisms governing transitioning between developmental stages are poorly understood. Each parasite stage can be distinguished by a characteristic transcriptional signature, with one signature being repressed during the other stages. Switching between stages require substantial changes in the proteome, which is achieved in part by ubiquitination. F-box proteins mediate protein poly-ubiquitination by recruiting substrates to SKP1, Cullin-1, F-Box protein E3 ubiquitin ligase (SCF-E3) complexes. We have identified an F-box protein named Toxoplasma gondii F-Box Protein L2 (TgFBXL2), which localizes to distinct perinucleolar sites. TgFBXL2 is stably engaged in an SCF-E3 complex that is surprisingly also associated with a COP9 signalosome complex that negatively regulates SCF-E3 function. At the cellular level, TgFBXL2-depleted parasites are severely defective in centrosome replication and daughter cell development. Most remarkable, RNAseq data show that TgFBXL2 conditional depletion induces the expression of stage-specific genes including a large cohort of genes necessary for sexual commitment. Together, these data suggest that TgFBXL2 is a latent guardian of stage specific gene expression in Toxoplasma and poised to remove conflicting proteins in response to an unknown trigger of development.

摘要

刚地弓形虫是一种食源性病原体,可导致胎儿和免疫功能低下患者发生严重且危及生命的感染。猫科动物是其唯一的终末宿主,而包括人类在内的广泛动物则作为中间宿主。当可传播的缓殖子阶段被猫科动物经口摄入时,它们会转化为裂殖子,无性繁殖,最终为寄生虫的有性周期产生数百万个配子。然而,中间宿主中的缓殖子仅分化为致病的速殖子,后者迅速在宿主中扩散。尽管速殖子已经得到了充分研究,但控制发育阶段之间转换的分子机制还知之甚少。每个寄生虫阶段都可以通过特征性转录特征来区分,其中一个特征在其他阶段被抑制。阶段之间的转换需要蛋白质组发生重大变化,部分是通过泛素化实现的。F-box 蛋白通过将底物招募到 SKP1、Cullin-1、F-Box 蛋白 E3 泛素连接酶 (SCF-E3) 复合物中来介导蛋白质多泛素化。我们已经鉴定出一种名为刚地弓形虫 F-Box 蛋白 L2 (TgFBXL2) 的 F-box 蛋白,它定位于独特的核周斑。TgFBXL2 稳定地参与 SCF-E3 复合物,该复合物令人惊讶地也与 COP9 信号体复合物相关联,后者负调控 SCF-E3 功能。在细胞水平上,TgFBXL2 耗尽的寄生虫在中心体复制和子细胞发育方面严重缺陷。最显著的是,RNAseq 数据显示,TgFBXL2 条件性耗尽诱导了阶段特异性基因的表达,包括一大群对有性发育至关重要的基因。总之,这些数据表明,TgFBXL2 是刚地弓形虫中阶段特异性基因表达的潜在守护者,并准备在受到未知发育触发时去除冲突蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bb/11166348/11395d1d0116/ppat.1012269.g001.jpg

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