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Updated: Jan 4, 2026

Author Spotlight: Identifying Compensatory Pathways in Malaria Parasites Containing Hypomorphic Allele of Essential Protein Kinases
Published on: November 22, 2024
Profiling Transcriptional Regulation and Functional Roles of Schistosoma mansoni c-Jun N-Terminal Kinase
Sandra Grossi Gava1, Naiara Clemente Tavares1, Franco Harald Falcone2,3
1Laboratório de Helmintologia e Malacologia Médica, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Brazil.
Abstract:
Mitogen-activated protein kinases (MAPKs) play a regulatory role and influence various biological activities, such as cell proliferation, differentiation, and survival. Our group has demonstrated through functional studies that Schistosoma mansoni c-Jun N-terminal kinase (SmJNK) MAPK is involved in the parasite's development, reproduction, and survival. SmJNK can, therefore, be considered a potential target for the development of new drugs. Considering the importance of SmJNK in S. mansoni maturation, we aimed at understanding of SmJNK regulated signaling pathways in the parasite, correlating expression data with S. mansoni development. To better understand the role of SmJNK in S. mansoni intravertebrate host life stages, RNA interference knockdown was performed in adult worms and in schistosomula larval stage. SmJNK knocked-down in adult worms showed a decrease in oviposition and no significant alteration in their movement. RNASeq libraries of SmJNK knockdown schistosomula were sequenced. A total of 495 differentially expressed genes were observed in the SmJNK knockdown parasites, of which 373 were down-regulated and 122 up-regulated. Among the down-regulated genes, we found transcripts related to protein folding, purine nucleotide metabolism, the structural composition of ribosomes and cytoskeleton. Genes coding for proteins that bind to nucleic acids and proteins involved in the phagosome and spliceosome pathways were enriched. Additionally, we found that SmJNK and Smp38 MAPK signaling pathways converge regulating the expression of a large set of genes. C. elegans orthologous genes were enriched for genes related to sterility and oocyte maturation, corroborating the observed phenotype alteration. This work allowed an in-depth analysis of the SmJNK signaling pathway, elucidating gene targets of regulation and functional roles of this critical kinase for parasite maturation.
Insights
Schistosoma mansoni c-Jun N-terminal kinase (SmJNK) is crucial for parasite development and survival. Targeting SmJNK signaling pathways could lead to new drugs against schistosomiasis by affecting parasite maturation and reproduction.
Area of Science:
- Parasitology
- Molecular Biology
- Biochemistry
Background:
- Mitogen-activated protein kinases (MAPKs) regulate vital cellular processes including proliferation, differentiation, and survival.
- Schistosoma mansoni c-Jun N-terminal kinase (SmJNK) has been implicated in parasite development, reproduction, and survival.
- SmJNK represents a potential drug target for schistosomiasis treatment.
Purpose of the Study:
- To elucidate the SmJNK signaling pathways regulating Schistosoma mansoni maturation.
- To correlate gene expression data with parasite development stages.
- To understand the functional role of SmJNK in the parasite's intravertebrate host life stages.
Main Methods:
- RNA interference (RNAi) knockdown of SmJNK in adult and schistosomula stages of S. mansoni.
- RNA sequencing (RNASeq) to analyze gene expression changes in SmJNK knockdown schistosomula.
- Bioinformatic analysis to identify differentially expressed genes and enriched pathways.
Main Results:
- SmJNK knockdown in adult worms reduced oviposition.
- RNASeq revealed 495 differentially expressed genes in SmJNK knockdown schistosomula (373 down-regulated, 122 up-regulated).
- Down-regulated genes were associated with protein folding, purine metabolism, ribosomes, cytoskeleton, phagosome, and spliceosome pathways; SmJNK and Smp38 MAPK pathways converge.
Conclusions:
- SmJNK plays a critical role in S. mansoni maturation and reproduction.
- The study identified key gene targets regulated by SmJNK signaling.
- Understanding SmJNK pathways offers insights for developing novel anti-schistosomiasis therapeutics.
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