Evidence map›Paper›PMID 39844208›Full record

ArticleGenome biology2025

Dynamic co-evolution of transposable elements and the piRNA pathway in African cichlid fishes.

Miguel Vasconcelos Almeida, Moritz Blumer, Chengwei Ulrika Yuan, Pío Sierra, Jonathan L Price, Fu Xiang Quah, Aleksandr Friman, Alexandra Dallaire, Grégoire Vernaz, Audrey L K Putman and 7 more

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Miguel Vasconcelos AlmeidaDepartment of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK. mdd34@cam.ac.uk.ORCID http://orcid.org/0000-0002-4816-3111
Moritz Blumer *Department of Genetics, University of Cambridge, Downing Street, Cambridge, CB2 3EH, UK.
Chengwei Ulrika Yuan *Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK.
Pío SierraDepartment of Genetics, University of Cambridge, Downing Street, Cambridge, CB2 3EH, UK.
Jonathan L PriceDepartment of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK.
Fu Xiang QuahDepartment of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK.
Aleksandr FrimanNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, 20892, USA.
Alexandra DallaireDepartment of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK.
Grégoire VernazWellcome/CRUK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QN, UK.
Audrey L K PutmanDepartment of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK.
Alan M SmithSchool of Natural Sciences, University of Hull, Hull, HU6 7RX, UK.
Domino A JoyceSchool of Natural Sciences, University of Hull, Hull, HU6 7RX, UK.
Falk ButterInstitute of Molecular Biology (IMB), Quantitative Proteomics, Ackermannweg 4, Mainz, 55128, Germany.
Astrid D HaaseNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, 20892, USA.
Richard DurbinDepartment of Genetics, University of Cambridge, Downing Street, Cambridge, CB2 3EH, UK.
M Emília SantosDepartment of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK.
Eric A MiskaDepartment of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, CB2 1GA, UK. eam29@cam.ac.uk.

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundEast African cichlid fishes have diversified in an explosive fashion, but the (epi)genetic basis of the phenotypic diversity of these fishes remains largely unknown. Although transposable elements (TEs) have been associated with phenotypic variation in cichlids, little is known about their transcriptional activity and epigenetic silencing. We set out to bridge this gap and to understand the interactions between TEs and their cichlid hosts.

resultsHere, we describe dynamic patterns of TE expression in African cichlid gonads and during early development. Orthology inference revealed strong conservation of TE silencing factors in cichlids, and an expansion of piwil1 genes in Lake Malawi cichlids, likely driven by PiggyBac TEs. The expanded piwil1 copies have signatures of positive selection and retain amino acid residues essential for catalytic activity. Furthermore, the gonads of African cichlids express a Piwi-interacting RNA (piRNA) pathway that targets TEs. We define the genomic sites of piRNA production in African cichlids and find divergence in closely related species, in line with fast evolution of piRNA-producing loci.

conclusionsOur findings suggest dynamic co-evolution of TEs and host silencing pathways in the African cichlid radiations. We propose that this co-evolution has contributed to cichlid genomic diversity.

Indexed as

CichlidsDNA Transposable ElementsEvolution, MolecularRNA, Small InterferingAnimalsArgonaute ProteinsGonadsPiwi-Interacting RNAArgonaute ProteinsDNA Transposable ElementsPiwi-Interacting RNARNA, Small Interfering

Identifiers

PMID39844208
PMCPMC11753138

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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.