Characterization of a Y‐specific duplication/insertion of the anti‐Mullerian hormone type II receptor gene based on a chromosome‐scale genome assembly of yellow perch, Perca flavescens

Yellow perch, Perca flavescens, is an ecologically and economically important species native to a large portion of the northern United States and southern Canada and is also a promising candidate species for aquaculture. However, no yellow perch reference genome has been available to facilitate impr...

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Published inMolecular ecology resources Vol. 20; no. 2; pp. 531 - 543
Main Authors Feron, Romain, Zahm, Margot, Cabau, Cédric, Klopp, Christophe, Roques, Céline, Bouchez, Olivier, Eché, Camille, Valière, Sophie, Donnadieu, Cécile, Haffray, Pierrick, Bestin, Anastasia, Morvezen, Romain, Acloque, Hervé, Euclide, Peter T., Wen, Ming, Jouano, Elodie, Schartl, Manfred, Postlethwait, John H., Schraidt, Claire, Christie, Mark R., Larson, Wesley A., Herpin, Amaury, Guiguen, Yann
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.03.2020
Wiley/Blackwell
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ISSN1755-098X
1755-0998
1755-0998
DOI10.1111/1755-0998.13133

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Summary:Yellow perch, Perca flavescens, is an ecologically and economically important species native to a large portion of the northern United States and southern Canada and is also a promising candidate species for aquaculture. However, no yellow perch reference genome has been available to facilitate improvements in both fisheries and aquaculture management practices. By combining Oxford Nanopore Technologies long‐reads, 10X Genomics Illumina short linked reads and a chromosome contact map produced with Hi‐C, we generated a high‐continuity chromosome‐scale yellow perch genome assembly of 877.4 Mb. It contains, in agreement with the known diploid chromosome yellow perch count, 24 chromosome‐size scaffolds covering 98.8% of the complete assembly (N50 = 37.4 Mb, L50 = 11). We also provide a first characterization of the yellow perch sex determination locus that contains a male‐specific duplicate of the anti‐Mullerian hormone type II receptor gene (amhr2by) inserted at the proximal end of the Y chromosome (chromosome 9). Using this sex‐specific information, we developed a simple PCR genotyping assay which accurately differentiates XY genetic males (amhr2by+) from XX genetic females (amhr2by−). Our high‐quality genome assembly is an important genomic resource for future studies on yellow perch ecology, toxicology, fisheries and aquaculture research. In addition, characterization of the amhr2by gene as a candidate sex‐determining gene in yellow perch provides a new example of the recurrent implication of the transforming growth factor beta pathway in fish sex determination, and highlights gene duplication as an important genomic mechanism for the emergence of new master sex determination genes.
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PMCID: PMC7050324
YG, MS, and JHP designed the project. WL, CS and MC collected the samples, EJ, MW, CR, OB, SV and HA extract the gDNA, made the genomic libraries and sequenced them. RF, CC, CK, MZ, PE, AH and YG processed the genome assemblies and / or analyzed the results. CS and MC checked sex-linkage of amhr2by on yellow perch samples. YG, RF, WL, MC, JHP, CC, CK, and CR wrote the manuscript. MS, JHP, CD, PH, AB, RM, MC and YG, supervised the project administration and raised funding. All the authors read and approved the final manuscript.
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ISSN:1755-098X
1755-0998
1755-0998
DOI:10.1111/1755-0998.13133