Liao Xiaolin, Xu Genbo, Chen Song-Lin
Key Laboratory for Sustainable Development of Marine Fisheries, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China.
Int J Mol Sci. 2014 Jul 22;15(7):12952-8. doi: 10.3390/ijms150712952.
Half-smooth tongue sole (Cynoglossus semilaevis) is one of the most important flatfish species for aquaculture in China. To produce a monosex population, we attempted to develop a marker-assisted sex control technique in this sexually size dimorphic fish. In this study, we identified a co-dominant sex-linked marker (i.e., CyseSLM) by screening genomic microsatellites and further developed a novel molecular method for sex identification in the tongue sole. CyseSLM has a sequence similarity of 73%-75% with stickleback, medaka, Fugu and Tetraodon. At this locus, two alleles (i.e., A244 and A234) were amplified from 119 tongue sole individuals with primer pairs CyseSLM-F1 and CyseSLM-R. Allele A244 was present in all individuals, while allele A234 (female-associated allele, FAA) was mostly present in females with exceptions in four male individuals. Compared with the sequence of A244, A234 has a 10-bp deletion and 28 SNPs. A specific primer (CyseSLM-F2) was then designed based on the A234 sequence, which amplified a 204 bp fragment in all females and four males with primer CyseSLM-R. A time-efficient multiplex PCR program was developed using primers CyseSLM-F2, CyseSLM-R and the newly designed primer CyseSLM-F3. The multiplex PCR products with co-dominant pattern could be detected by agarose gel electrophoresis, which accurately identified the genetic sex of the tongue sole. Therefore, we have developed a rapid and reliable method for sex identification in tongue sole with a newly identified sex-linked microsatellite marker.
半滑舌鳎(Cynoglossus semilaevis)是中国水产养殖中最重要的鲆鲽类物种之一。为了培育单性种群,我们试图在这种具有性别大小二态性的鱼类中开发一种标记辅助性别控制技术。在本研究中,我们通过筛选基因组微卫星鉴定了一个共显性的性别连锁标记(即CyseSLM),并进一步开发了一种用于舌鳎性别鉴定的新分子方法。CyseSLM与刺鱼、青鳉、河豚和密斑刺鲀的序列相似性为73%-75%。在该位点,用引物对CyseSLM-F1和CyseSLM-R从119个舌鳎个体中扩增出两个等位基因(即A244和A234)。等位基因A244存在于所有个体中,而等位基因A234(雌性相关等位基因,FAA)大多存在于雌性个体中,有4个雄性个体例外。与A244的序列相比,A234有一个10 bp的缺失和28个单核苷酸多态性。然后根据A234序列设计了一个特异性引物(CyseSLM-F2),该引物与引物CyseSLM-R一起在所有雌性个体和4个雄性个体中扩增出一个204 bp的片段。使用引物CyseSLM-F2、CyseSLM-R和新设计的引物CyseSLM-F3开发了一种高效的多重PCR程序。具有共显性模式的多重PCR产物可通过琼脂糖凝胶电泳检测,从而准确鉴定舌鳎的遗传性别。因此,我们利用新鉴定的性别连锁微卫星标记开发了一种快速可靠的舌鳎性别鉴定方法。