首页> 外文期刊>Marine biotechnology >Identification, Characterization, and Mapping of a Novel SNP Associated with Body Color Transparency in Juvenile Red Sea Bream ( Emphasis Type='Italic'>Pagrus major/Emphasis>)
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Identification, Characterization, and Mapping of a Novel SNP Associated with Body Color Transparency in Juvenile Red Sea Bream ( Emphasis Type='Italic'>Pagrus major/Emphasis>)

机译:与少年红海鲷(&强调=“斜体”> Pagrus Major)与人体颜色透明度相关的新型SNP的鉴定,表征和映射。/ PAGRUS>)

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We previously reported a body color deformity in juvenile red sea bream, which shows transparency in the juvenile stage because of delayed chromatophore development compared with normal individuals, and this finding suggested a genetic cause based on parentage assessments. To conduct marker-assisted selection to eliminate broodstock inheriting the causative gene, developing DNA markers associated with the phenotype was needed. We first conducted SNP mining based on AFLP analysis using bulked-DNA from normal and transparent individuals. One SNP was identified from a transparent-specific AFLP fragment, which significantly associated with transparent individuals. Two alleles (A/G) were observed in this locus, and the genotype G/G was dominantly observed in the transparent groups (97.1%) collected from several production lots produced from different broodstock populations. A few normal individuals inherited the G/G genotype (5.0%), but the A/A and A/G genotypes were dominantly observed in the normal groups. The homologs region of the SNP was searched using a medaka genome database, and intron 12 of the Nell2a gene (located on chromosome 6 of the medaka genome) was highly matched. We also mapped the red sea bream Nell2a gene on the previously developed linkage maps, and this gene was mapped on a male linkage group, LG4-M. The newly found SNP was useful in eliminating broodstock possessing the causative gene of the body color transparency observed in juvenile stage of red sea bream.
机译:我们之前报道了少年红海鲷的身体颜色畸形,其显示少年阶段的透明度,因为染色体发育与正常人相比,这一发现提出了基于父母评估的遗传原因。为了进行标记辅助选择以消除遗传致病基因的黄蜂,需要开发与表型相关的DNA标志物。我们首先通过来自正常和透明个体的膨胀DNA进行AFLP分析进行SNP挖掘。从透明特异性AFLP片段中鉴定一个SNP,其与透明个体显着相关。在该基因座中观察到两种等位基因(A / g),并且在由不同亲属种群产生的几种生产批次中收集的透明基团(97.1%)中,基因型G / g在透明基团中占主导地位。几个正常的个体遗传了G / g基因型(5.0%),但在正常组中占主导地位A / A和A / G基因型。使用Medaka基因组数据库搜索SNP的同源区域,并且NELL2A基因的内含子12(位于Medaka Genome的染色体6上)高匹配。我们还将红海鲷NELL2A基因映射到以前显影的联动地图上,并且该基因映射在雄性连杆基团LG4-M上。新发现的SNP可用于消除在红海鲷的少年阶段观察到的具有身体颜色透明度的致病基因的亲密衣服。

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