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March 14, 2026Non-Coding RNA0 citationsOpen Access

Comprehensive Schistosoma mansoni Hierarchical Transcriptome Assembly Points to Novel lncRNAs Associated with Sexual Dimorphism

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CFCaio Felipe FreireTSThalles Souza-LopesMAMurilo Sena Amaral

Key Points

  • The aim is to identify novel long noncoding RNAs (lncRNAs) in Schistosoma mansoni that are associated with sexual dimorphism to uncover new therapeutic targets.
  • Compiled RNA-seq data from the Sequence Read Archive (SRA)
  • Performed hierarchical transcriptome assembly using the multi-sample assembler Ryūtō
  • Applied HOMER for peak-calling and histone marks identification
  • Used weighted gene co-expression network analysis (WGCNA) for lncRNA functional inference
  • Identified 10,170 novel lncRNA genes and 16,990 novel lncRNA transcripts
  • Most lncRNAs (78.7%) have histone regulatory marks near transcription start sites
  • Found 1991 differentially expressed genes, including 339 novel lncRNAs
  • Gene Ontology analyses suggest involvement in cell differentiation and morphogenesis pathways

Abstract

Background/Objectives: Schistosomiasis is a neglected tropical disease affecting >200 million people worldwide. Praziquantel is the sole recommended drug against Schistosoma mansoni; however, it lacks activity against juvenile forms and cannot prevent reinfection. Thus, there is an urgent need to identify novel therapeutic targets. Long noncoding RNAs (lncRNAs) are known to regulate various biological processes in S. mansoni, including parasite pairing and fertility; therefore, screening for novel lncRNAs could reveal new potential targets. Methods: We compiled all publicly available RNA-seq data from the Sequence Read Archive (SRA) and performed a hierarchical transcriptome assembly using the multi-sample assembler Ryūtō, combined with version 10 of the S. mansoni genome. We applied HOMER for peak-calling and identification of histone marks and used weighted gene co-expression network analysis (WGCNA) to infer putative functions of lncRNAs in sexual dimorphism. Results: Using a robust pipeline, we identified 10,170 novel lncRNA genes comprising 16,990 novel lncRNA transcripts, including 8783 intergenic, 7918 antisense, and 289 intronic lncRNA transcripts. Most (78.7%) have histone regulatory marks (H3K4me3, H3K27me3, H3K27ac, or H4K20me1) near their transcription start sites, indicating potential expression regulation. Comparing male and female samples, we identified 1991 differentially expressed genes (FDR < 5%, |log2FC| ≥ 1.5), including 296 known lncRNAs and 339 novel lncRNAs. WGCNA identified hub lncRNAs within co-expression modules, and Gene Ontology enrichment analyses (FDR ≤ 5%) suggest that these lncRNAs are involved in cell differentiation and morphogenesis pathways. Conclusions: We provide a comprehensive catalog of S. mansoni lncRNAs. These findings offer opportunities to discover potential new therapeutic targets, advancing the future development of anti-schistosome therapies.

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Cite This Study

Freire et al. (2026) studied this question.

synapsesocial.com/papers/69b4fc1fb39f7826a300cc36https://doi.org/10.3390/ncrna12020009
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