Evidence for holocentric centromeres in the early branching apicomplexan parasite Cryptosporidium parvum

During its asexual cycle, Cryptosporidium parvum (C. parvum) amplifies through three rounds of nuclear division before undergoing cytokinesis to form infectious merozoites. However, chromosome organization and segregation during nuclear division remain poorly studied. Here, we visualized H3-histones, including the centromeric histone H3 (CENH3), telomeres, and centrosomes during mitosis. Nuclear division was accompanied by centrosome duplication and elongated microtubules that spanned the dividing nuclei. Surprisingly, C. parvum centromeres detected by CENH3 showed diffuse staining throughout nuclear division and overlapped with telomeres in the apical nucleus. Analysis of centromeres based on CENH3 capture and DNA sequencing revealed numerous distinct binding sites scattered across all eight chromosomes, including both coding regions and intergenic regions, which were typified by GA rich repeat sequences. The unique holocentric chromosome structure of C. parvum is unlike the single regional centromeres found in related apicomplexans, suggesting it arose independently from other known examples in plants, insects and worms.

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Journal
PLoS Pathogens
Published
2026-10-26
DOI
https://doi.org/10.1371/journal.ppat.1014708
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
0.00

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article

Evidence for holocentric centromeres in the early branching apicomplexan parasite Cryptosporidium parvum

Melanie Key, L. David Sibley, Lisa J. Funkhouser-Jones, Abigail K. Kimball et al.
PLoS Pathogens
Chromosomal and Genetic Variations
article

Evidence for holocentric centromeres in the early branching apicomplexan parasite Cryptosporidium parvum

Melanie Key, L. David Sibley, Lisa J. Funkhouser-Jones, Abigail K. Kimball, Rui Xu, Wanyi Huang
article en

Abstract

During its asexual cycle, Cryptosporidium parvum (C. parvum) amplifies through three rounds of nuclear division before undergoing cytokinesis to form infectious merozoites. However, chromosome organization and segregation during nuclear division remain poorly studied. Here, we visualized H3-histones, including the centromeric histone H3 (CENH3), telomeres, and centrosomes during mitosis. Nuclear division was accompanied by centrosome duplication and elongated microtubules that spanned the dividing nuclei. Surprisingly, C. parvum centromeres detected by CENH3 showed diffuse staining throughout nuclear division and overlapped with telomeres in the apical nucleus. Analysis of centromeres based on CENH3 capture and DNA sequencing revealed numerous distinct binding sites scattered across all eight chromosomes, including both coding regions and intergenic regions, which were typified by GA rich repeat sequences. The unique holocentric chromosome structure of C. parvum is unlike the single regional centromeres found in related apicomplexans, suggesting it arose independently from other known examples in plants, insects and worms.

PLoS PathogensVol. 22(10)
Washington University in St. Louis (US)
National Science Foundation, Washington University in St. Louis, South China Agricultural University, National Institutes of Health, Washington University School of Medicine in St. Louis, Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Science Foundation Graduate Research Fellowship Program
Openalex Percentile: Top 14%
Chromosomal and Genetic Variations
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