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Background <p><i>Trypanosoma cruzi</i>, the etiological agent of Chagas disease, possesses a highly repetitive genome that has historically hindered high-quality assembly and structural characterization. Despite significant advances in assembling <i>T. cruzi</i> genomes, major gaps remain. Among these, the complete repertoire of centromeric sequences has remained elusive, representing a critical missing piece in our understanding of chromosome structure and inheritance.</p> Results <p>Here, we generated high-coverage Hi-C (genome-wide chromosome conformation capture) data for the widely used <i>T. cruzi</i> Dm28c strain improving its genome assembly by scaffolding contigs and producing a more contiguous and accurate genome. To investigate centromere organization, we performed ChIP-seq using the mNeonGreen-myc-tagged kinetochore proteins KKT2 and KKT3, resulting in the identification of 33 KKT-enriched peaks across 27 scaffolds. These peaks were located in regions enriched in retrotransposable elements, particularly L1Tc and VIPER, near strand switch regions, areas of high GC content, and in 51% of the cases at the transitional regions between conserved genes and virulence-factor multigene families. Notably, Hi-C analysis shows that candidate centromeric regions are frequently positioned between genomic domains with distinct 3D interaction profiles suggesting that they may contribute to genome compartmentalization, and frequently engage in 3D spatial clustering, suggesting a role in higher-order nuclear architecture.</p> Conclusion <p>Overall, our study provides a high-quality reference genome for the Dm28c strain, presents the first genome-wide centromere map in <i>T. cruzi</i>, and offers novel insights into centromere-mediated 3D genome organization.</p>

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First genome-wide centromere map of Trypanosoma cruzi suggests linear and 3D compartment boundaries and spatial clustering

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年6月17日

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  • Natália Karla Bellini,
  • Pedro Gabriel Nachtigall,
  • Pedro Leonardo Carvalho de Lima,
  • Herbert Guimarães de Sousa Silva,
  • David da Silva Pires,
  • Vinicius Carius de Souza,
  • Claudia Rabuffo,
  • Danielle Bruno de Carvalho,
  • Yasmin Morais Feno,
  • Ana Paula Cabral de Araujo Lima,
  • T. Nicolai Siegel,
  • Julia Pinheiro Chagas da Cunha

摘要

Background

Trypanosoma cruzi, the etiological agent of Chagas disease, possesses a highly repetitive genome that has historically hindered high-quality assembly and structural characterization. Despite significant advances in assembling T. cruzi genomes, major gaps remain. Among these, the complete repertoire of centromeric sequences has remained elusive, representing a critical missing piece in our understanding of chromosome structure and inheritance.

Results

Here, we generated high-coverage Hi-C (genome-wide chromosome conformation capture) data for the widely used T. cruzi Dm28c strain improving its genome assembly by scaffolding contigs and producing a more contiguous and accurate genome. To investigate centromere organization, we performed ChIP-seq using the mNeonGreen-myc-tagged kinetochore proteins KKT2 and KKT3, resulting in the identification of 33 KKT-enriched peaks across 27 scaffolds. These peaks were located in regions enriched in retrotransposable elements, particularly L1Tc and VIPER, near strand switch regions, areas of high GC content, and in 51% of the cases at the transitional regions between conserved genes and virulence-factor multigene families. Notably, Hi-C analysis shows that candidate centromeric regions are frequently positioned between genomic domains with distinct 3D interaction profiles suggesting that they may contribute to genome compartmentalization, and frequently engage in 3D spatial clustering, suggesting a role in higher-order nuclear architecture.

Conclusion

Overall, our study provides a high-quality reference genome for the Dm28c strain, presents the first genome-wide centromere map in T. cruzi, and offers novel insights into centromere-mediated 3D genome organization.