TY - JOUR
T1 - Species and population genomic differentiation in Pocillopora corals (Cnidaria, Hexacorallia)
AU - Aurelle, Didier
AU - Pratlong, Marine
AU - Oury, Nicolas
AU - Haguenauer, Anne
AU - Gélin, Pauline
AU - Magalon, Hélène
AU - Adjeroud, Mehdi
AU - Romans, Pascal
AU - Vidal-Dupiol, Jeremie
AU - Claereboudt, Michel
AU - Noûs, Camille
AU - Reynes, Lauric
AU - Toulza, Eve
AU - Bonhomme, François
AU - Mitta, Guillaume
AU - Pontarotti, Pierre
N1 - Funding Information:
We thank Nicolas Fernandez and Béatrice Loriod from the Marseille TGML platform for their invaluable help and advices with the preparation of the RAD libraries. We thank the team of the MGX platform for the sequencing of the RAD libraries. We acknowledge Stéphanie Rialle, Maurine Bonabaud from the MGX sequencing platform (CNRS, Montpellier, France) for help with data production and quality controls. The authors thank the UMR 8199 LIGAN-PM Genomics group (Lille, France, especially Véronique Dhennin), who belongs to the ‘Federation de Recherche’ 3508 Labex EGID (European Genomics Institute for Diabetes; ANR-10-LABX-46) and was supported by the ANR Equipex 2010 session (ANR-10-EQPX-07-01; ‘LIGAN-PM’). The LIGAN-PM Genomics platform (Lille, France) is also supported by the FEDER and the Region Nord-Pas-de-Calais-Picardie. We acknowledge the staff of the “Cluster de calcul intensif HPC” Platform of the OSU Institut Pythéas (Aix-Marseille Université, INSU-CNRS) for facilitating the use of computing facilities. We gratefully acknowledge Julien Lecubin and Christophe Yohia from the Informatic Service of Pythéas Institute (SIP) for their technical assistance. We thank the molecular biology service of the IMBE. We are grateful to the genotoul bioinformatics platform Toulouse Occitanie (Bioinfo Genotoul, https://doi.org/10.15454/1.5572369328961167E12 ) for providing help and computing resources.
Funding Information:
This work is a contribution to the Labex OT-Med (n° ANR-11-LABX-0061) funded by the French Government “Investissements d’Avenir” program of the French National Research Agency (ANR) through the A*MIDEX project (n° ANR-11-IDEX-0001–02). This project has been funded by the ADACNI program of the French National Research Agency (ANR) (project n°ANR-12-ADAP-0016; http://adacni.imbe.fr ). The project leading to this publication has received funding from the European FEDER Fund under project 1166–39417. The authors acknowledge the financial support from the France Génomique National Infrastructure, funded as part of “Investissement d’Avenir” program managed by the Agence Nationale de la Recherche (contract ANR-10-INBS-09). This study was set within the framework of the Laboratoire d’Excellence (LABEX) TULIP (ANR-10-LABX-41).
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature Switzerland AG.
PY - 2022
Y1 - 2022
N2 - Correctly delimiting species and populations is a prerequisite for studies of connectivity, adaptation and conservation. Genomic data are particularly useful to test species differentiation for organisms with few informative morphological characters or low discrimination of cytoplasmic markers, as in Scleractinians. Here we applied Restriction site Associated DNA sequencing (RAD-sequencing) to the study of species differentiation and genetic structure in populations of Pocillopora spp. from Oman and French Polynesia, with the objectives to test species hypotheses, and to study the genetic structure among sampling sites within species. We focused here on coral colonies morphologically similar to P. acuta (damicornis type β). We tested the impact of different filtering strategies on the stability of the results. The main genetic differentiation was observed between samples from Oman and French Polynesia. These samples corresponded to different previously defined primary species hypotheses (PSH), i.e., PSHs 12 and 13 in Oman, and PSH 5 in French Polynesia. In Oman, we did not observe any clear differentiation between the two putative species PSH 12 and 13, nor between sampling sites. In French Polynesia, where a single species hypothesis was studied, there was no differentiation between sites. Our analyses allowed the identification of clonal lineages in Oman and French Polynesia. The impact of clonality on genetic diversity is discussed in light of individual-based simulations.
AB - Correctly delimiting species and populations is a prerequisite for studies of connectivity, adaptation and conservation. Genomic data are particularly useful to test species differentiation for organisms with few informative morphological characters or low discrimination of cytoplasmic markers, as in Scleractinians. Here we applied Restriction site Associated DNA sequencing (RAD-sequencing) to the study of species differentiation and genetic structure in populations of Pocillopora spp. from Oman and French Polynesia, with the objectives to test species hypotheses, and to study the genetic structure among sampling sites within species. We focused here on coral colonies morphologically similar to P. acuta (damicornis type β). We tested the impact of different filtering strategies on the stability of the results. The main genetic differentiation was observed between samples from Oman and French Polynesia. These samples corresponded to different previously defined primary species hypotheses (PSH), i.e., PSHs 12 and 13 in Oman, and PSH 5 in French Polynesia. In Oman, we did not observe any clear differentiation between the two putative species PSH 12 and 13, nor between sampling sites. In French Polynesia, where a single species hypothesis was studied, there was no differentiation between sites. Our analyses allowed the identification of clonal lineages in Oman and French Polynesia. The impact of clonality on genetic diversity is discussed in light of individual-based simulations.
KW - Clonal reproduction
KW - Coral
KW - Genetic structure
KW - Pocillopora
KW - RAD-sequencing
KW - Species delineation
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U2 - 10.1007/s10709-022-00165-7
DO - 10.1007/s10709-022-00165-7
M3 - Article
C2 - 36083388
AN - SCOPUS:85137839673
SN - 0016-6707
JO - Genetica
JF - Genetica
ER -