Single-cell transcriptomics reveal transcriptional programs underlying male and female cell fate during Plasmodium falciparum gametocytogenesis.
Mubasher MohammedAlexis DziedziechDiego MacedoFrederik HuppertzYlva VeithZoé PostelElena ChristRichard ScheyttTanja SlotteJohan HenrikssonJohan AnkarklevPublished in: Nature communications (2024)
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.
Keyphrases
- plasmodium falciparum
- single cell
- rna seq
- transcription factor
- high throughput
- endothelial cells
- genome wide
- gene expression
- network analysis
- public health
- cell fate
- genome wide identification
- heat shock
- mesenchymal stem cells
- dengue virus
- dna methylation
- genome wide analysis
- pluripotent stem cells
- current status
- zika virus
- dna binding