Abstract
In this study, we first identified male-specific SNP markers using restriction site-associated DNA sequencing, and further developed a PCR-based sex identification technique for Charybdis feriatus. A total of 296.96 million clean reads were obtained, with 114.95 and 182.01 million from females and males. After assembly and alignment, 10 SNP markers were identified being heterozygous in males but homozygous in females. Five markers were further confirmed to be male-specific in a large number of individuals. Moreover, two male-specific sense primers and a common antisense primer were designed, using which, a PCR-based genetic sex identification method was successfully developed and used to identify the sex of 103 individuals, with a result of 49 females and 54 males. The presence of male-specific SNP markers suggests an XX/XY sex determination system for C. feriatus. These findings should be helpful for better understanding sex determination mechanism, and drafting artificial breeding program in crustaceans.
•We first identified male-specific SNP markers using restriction site-associated DNA sequencing.•We developed a PCR-based sex identification technique for Charybdis feriatus.•After assembly and alignment, 10 SNP markers were identified being heterozygous in males but homozygous in females.•Five markers were further confirmed to be male-specific in a large number of individuals.•A PCR-based genetic sex identification method was successfully developed.