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单细胞转录组学揭示了疟原虫配子发生过程中雄性和雌性细胞命运的转录程序。

Single-cell transcriptomics reveal transcriptional programs underlying male and female cell fate during Plasmodium falciparum gametocytogenesis.

机构信息

Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.

Department of Global Health, Institut Pasteur, 25-28 Rue du Docteur Roux, Paris, France.

出版信息

Nat Commun. 2024 Aug 26;15(1):7177. doi: 10.1038/s41467-024-51201-3.

Abstract

The Plasmodium falciparum life cycle includes obligate transition between a human and mosquito host. Gametocytes are responsible for transmission from the human to the mosquito vector where gamete fusion followed by meiosis occurs. To elucidate how male and female gametocytes differentiate in the absence of sex chromosomes, we perform FACS-based cell enrichment of a P. falciparum gametocyte reporter line followed by single-cell RNA-seq. In our analyses we define the transcriptional programs and predict candidate driver genes underlying male and female development, including genes from the ApiAP2 family of transcription factors. A motif-driven, gene regulatory network analysis indicates that AP2-G5 specifically modulates male development. Additionally, genes linked to the inner membrane complex, involved in morphological changes, are uniquely expressed in the female lineage. The transcriptional programs of male and female development detailed herein allow for further exploration of the evolution of sex in eukaryotes and provide targets for future development of transmission blocking therapies.

摘要

疟原虫生命周期包括在人类和蚊子宿主之间的强制性转换。配子是负责从人类传播到蚊子媒介的,其中发生配子融合和减数分裂。为了阐明在没有性染色体的情况下雄性和雌性配子体如何分化,我们进行了基于 FACS 的疟原虫配子体报告系细胞富集,然后进行单细胞 RNA-seq。在我们的分析中,我们定义了转录程序,并预测了雄性和雌性发育的候选驱动基因,包括转录因子 ApiAP2 家族的基因。基于基序的基因调控网络分析表明,AP2-G5 特异性调节雄性发育。此外,与内膜复合物相关的基因,参与形态变化,仅在雌性谱系中表达。本文详细描述的雄性和雌性发育的转录程序允许进一步探索真核生物中性别进化,并为未来传播阻断疗法的发展提供目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2af/11347709/ed2c002ba089/41467_2024_51201_Fig1_HTML.jpg

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