The evolution of two transmissible leukaemias colonizing the coasts of Europe

Author:

Bruzos Alicia L.ORCID,Santamarina MartínORCID,García-Souto DanielORCID,Díaz SeilaORCID,Rocha SaraORCID,Zamora JorgeORCID,Lee YunahORCID,Viña-Feás Alejandro,Quail Michael A.ORCID,Otero IagoORCID,Pequeño-Valtierra AnaORCID,Temes JavierORCID,Rodriguez-Castro JorgeORCID,Villanueva Antonio,Costas DamiánORCID,Rodríguez Rosana,Prieto TamaraORCID,Tomás LauraORCID,Alvariño PilarORCID,Alonso Juana,Cao AsunciónORCID,Iglesias DavidORCID,Carballal María J.,Amaral Ana M.ORCID,Balseiro PabloORCID,Calado RicardoORCID,El Khalfi BouchraORCID,Izagirre UrtziORCID,de Montaudouin Xavier,Pade Nicolas G.ORCID,Probert IanORCID,Ricardo FernandoORCID,Ruiz PamelaORCID,Skazina MariaORCID,Smolarz KatarzynaORCID,Pasantes Juan J.ORCID,Villalba AntonioORCID,Ning ZeminORCID,Ju Young SeokORCID,Posada DavidORCID,Demeulemeester JonasORCID,Baez-Ortega AdrianORCID,Tubio Jose M. C.ORCID

Abstract

AbstractTransmissible cancers are malignant cell clones that spread among individuals through transfer of living cancer cells. Several such cancers, collectively known as bivalve transmissible neoplasia (BTN), are known to infect and cause leukaemia in marine bivalve molluscs. This is the case of BTN clones affecting the common cockle,Cerastoderma edule, which inhabits the Atlantic coasts of Europe and north-west Africa. To investigate the origin and evolution of contagious cancers in common cockles, we collected 6,854C. edulespecimens and diagnosed 390 cases of BTN. We then generated a reference genome for the species and assessed genomic variation in the genomes of 61 BTN tumours. Analysis of tumour-specific variants confirmed the existence of two cockle BTN lineages with independent clonal origins, and gene expression patterns supported their status as haemocyte-derived marine leukaemias. Examination of mitochondrial DNA sequences revealed several mitochondrial capture events in BTN, as well as co-infection of cockles by different tumour lineages. Mutational analyses identified two lineage-specific mutational signatures, one of which resembles a signature associated with DNA alkylation. Karyotypic and copy number analyses uncovered genomes marked by pervasive instability and polyploidy. Whole-genome duplication, amplification of oncogenesCCND3andMDM2, and deletion of the DNA alkylation repair geneMGMT, are likely drivers of BTN evolution. Characterization of satellite DNA identified elements with vast expansions in the cockle germ line, yet absent from BTN tumours, suggesting ancient clonal origins. Our study illuminates the evolution of contagious cancers under the sea, and reveals long-term tolerance of extreme instability in neoplastic genomes.

Publisher

Cold Spring Harbor Laboratory

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