Identification of the sex‐determining region in flathead grey mullet (Mugil cephalus). (9th September 2016)

• Record Type: Journal Article
• Authors: Dor, L.; Shirak, A.; Rosenfeld, H.; Ashkenazi, I. M.; Band, M. R.; Korol, A.; Ronin, Y.; Seroussi, E.; Weller, J. I.; Ron, M.
• Is Part Of: Animal genetics. Volume 47:Number 6(2016)
• Page Start: 698
• Page End: 707
• Publication Date: 2016-09-09
• Subjects: comparative mapping -- linkage map -- microsatellite markers -- fine mapping -- sex‐determining system; Animal genetics -- Periodicals; 572.8
• DOI: 10.1111/age.12486
• Languages: English
• ISSNs: 0268-9146

Abstract

Summary: Elucidation of the sex‐determination mechanism in flathead grey mullet ( Mugil cephalus ) is required to exploit its economic potential by production of genetically determined monosex populations and application of hormonal treatment to parents rather than to the marketed progeny. Our objective was to construct a first‐generation linkage map of the M. cephalus in order to identify the sex‐determining region and sex‐determination system. Deep‐sequencing data of a single male was assembled and aligned to the genome of Nile tilapia ( Oreochromis niloticus ). A total 245 M. cephalus microsatellite markers were designed, spanning the syntenic tilapia genome assembly at intervals of 10 Mb. In the mapping family of full‐sib progeny, 156 segregating markers were used to construct a first‐generation linkage map of 24 linkage groups (LGs), corresponding to the number of chromosomes. The linkage map spanned approximately 1200 cM with an average inter‐marker distance of 10.6 cM. Markers segregating on LG9 in two independent mapping families showed nearly complete concordance with gender ( R 2 = 0.95). The sex determining locus was fine mapped within an interval of 8.6 cM on LG9. The sex of offspring was determined only by the alleles transmitted from the father, thus indicating an XY sex‐determination system.