Evidence map›Paper›PMID 38413905›Full record

ArticleBMC genomics2024

Subtelomeric plasticity contributes to gene family expansion in the human parasitic flatworm Schistosoma mansoni.

T Brann, A Beltramini, C Chaparro, M Berriman, S R Doyle, A V Protasio

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Paralogs of thebioRxiv : the preprint server for biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

T BrannDepartment of Pathology, University of Cambridge, Cambridge, CB1 2PQ, UK.
A BeltraminiDepartment of Pathology, University of Cambridge, Cambridge, CB1 2PQ, UK.
C ChaparroIHPE, CNRS, IFREMER, UPVD, University Montpellier, Perpignan, F-66860, France.
M BerrimanSchool of Infection and Immunity, University of Glasgow, Glasgow, G12 8TA, UK.
S R DoyleWellcome Sanger Institute, Cambridge, CB10 1SA, UK.
A V ProtasioDepartment of Pathology, University of Cambridge, Cambridge, CB1 2PQ, UK. avp25@cam.ac.uk.
University of Cambridge · GBCentre National de la Recherche Scientifique · FRUniversity of Glasgow · GBWellcome Sanger Institute · GB

Funding

Medical Research Council MR/T020733/1Wellcome TrustWellcome Trust 206194
6 · The paper itself

Abstract

backgroundThe genomic region that lies between the telomere and chromosome body, termed the subtelomere, is heterochromatic, repeat-rich, and frequently undergoes rearrangement. Within this region, large-scale structural changes enable gene diversification, and, as such, large multicopy gene families are often found at the subtelomere. In some parasites, genes associated with proliferation, invasion, and survival are often found in these regions, where they benefit from the subtelomere's highly plastic, rapidly changing nature. The increasing availability of complete (or near complete) parasite genomes provides an opportunity to investigate these typically poorly defined and overlooked genomic regions and potentially reveal relevant gene families necessary for the parasite's lifestyle.

resultsUsing the latest chromosome-scale genome assembly and hallmark repeat richness observed at chromosome termini, we have identified and characterised the subtelomeres of Schistosoma mansoni, a metazoan parasitic flatworm that infects over 250 million people worldwide. Approximately 12% of the S. mansoni genome is classified as subtelomeric, and, in line with other organisms, we find these regions to be gene-poor but rich in transposable elements. We find that S. mansoni subtelomeres have undergone extensive interchromosomal recombination and that these sites disproportionately contribute to the 2.3% of the genome derived from segmental duplications. This recombination has led to the expansion of subtelomeric gene clusters containing 103 genes, including the immunomodulatory annexins and other gene families with unknown roles. The largest of these is a 49-copy plexin domain-containing protein cluster, exclusively expressed in the tegument-the tissue located at the host-parasite physical interface-of intramolluscan life stages.

conclusionsWe propose that subtelomeric regions act as a genomic playground for trial-and-error of gene duplication and subsequent divergence. Owing to the importance of subtelomeric genes in other parasites, gene families implicated in this subtelomeric expansion within S. mansoni warrant further characterisation for a potential role in parasitism.

Indexed as

Schistosoma mansoniTelomereAnimalsGene DuplicationGenomicsHumansMultigene FamilyGenomic repeatsNon-allelic homologous recombinationSchistosoma mansoniSegmental duplicationSubtelomereTransposable element

Identifiers

PMID38413905
PMCPMC10900676
OpenAlexW4392200393

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.