Department of Medicine, Mie University, Tsu 514-8507, Japan.
Research Institute for Microbial Diseases, Osaka University, Suita 565-0871, Japan.
Nucleic Acids Res. 2024 Jun 10;52(10):5624-5642. doi: 10.1093/nar/gkae207.
Gametocyte development of the Plasmodium parasite is a key step for transmission of the parasite. Male and female gametocytes are produced from a subpopulation of asexual blood-stage parasites, but the mechanisms that regulate the differentiation of sexual stages are still under investigation. In this study, we investigated the role of PbARID, a putative subunit of a SWI/SNF chromatin remodeling complex, in transcriptional regulation during the gametocyte development of P. berghei. PbARID expression starts in early gametocytes before the manifestation of male and female-specific features, and disruption of its gene results in the complete loss of gametocytes with detectable male features and the production of abnormal female gametocytes. ChIP-seq analysis of PbARID showed that it forms a complex with gSNF2, an ATPase subunit of the SWI/SNF chromatin remodeling complex, associating with the male cis-regulatory element, TGTCT. Further ChIP-seq of PbARID in gsnf2-knockout parasites revealed an association of PbARID with another cis-regulatory element, TGCACA. RIME and DNA-binding assays suggested that HDP1 is the transcription factor that recruits PbARID to the TGCACA motif. Our results indicated that PbARID could function in two chromatin remodeling events and paly essential roles in both male and female gametocyte development.
疟原虫配子体的发育是寄生虫传播的关键步骤。雄配子体和雌配子体是由无性血期寄生虫的亚群产生的,但调节性阶段分化的机制仍在研究中。在这项研究中,我们研究了 PbARID 在 P. berghei 配子体发育过程中的转录调控作用,PbARID 是一个 SWI/SNF 染色质重塑复合物的假定亚基。PbARID 的表达始于早期配子体中,早于出现雄性和雌性特异性特征之前,其基因的破坏导致完全丧失可检测的雄性特征的配子体和产生异常的雌性配子体。PbARID 的 ChIP-seq 分析表明,它与 gSNF2 形成复合物,gSNF2 是 SWI/SNF 染色质重塑复合物的 ATP 酶亚基,与雄性顺式调控元件 TGTCT 结合。在 gsnf2 敲除寄生虫中的 PbARID 进一步 ChIP-seq 显示,PbARID 与另一个顺式调控元件 TGCACA 结合。RIME 和 DNA 结合测定表明,HDP1 是招募 PbARID 到 TGCACA 基序的转录因子。我们的结果表明,PbARID 可以在两个染色质重塑事件中发挥作用,并在雄性和雌性配子体发育中发挥重要作用。