Ulloa Pilar E, Rincón Gonzalo, Islas-Trejo Alma, Araneda Cristian, Iturra Patricia, Neira Roberto, Medrano Juan F
Programa de Doctorado en Ciencias de Recursos Naturales, Universidad de La Frontera, Casilla 54-D, Temuco, Chile,
Mar Biotechnol (NY). 2015 Jun;17(3):353-63. doi: 10.1007/s10126-015-9624-1. Epub 2015 Feb 22.
The objectives of this study were to measure gene expression in zebrafish and then identify SNP to be used as potential markers in a growth association study. We developed an approach where muscle samples collected from low- and high-growth fish were analyzed using RNA-Sequencing (RNA-seq), and SNP were chosen from the genes that were differentially expressed between the low and high groups. A population of 24 families was fed a plant protein-based diet from the larval to adult stages. From a total of 440 males, 5 % of the fish from both tails of the weight gain distribution were selected. Total RNA was extracted from individual muscle of 8 low-growth and 8 high-growth fish. Two pooled RNA-Seq libraries were prepared for each phenotype using 4 fish per library. Libraries were sequenced using the Illumina GAII Sequencer and analyzed using the CLCBio genomic workbench software. One hundred and twenty-four genes were differentially expressed between phenotypes (p value < 0.05 and FDR < 0.2). From these genes, 164 SNP were selected and genotyped in 240 fish samples. Marker-trait analysis revealed 5 SNP associated with growth in key genes (Nars, Lmod2b, Cuzd1, Acta1b, and Plac8l1). These genes are good candidates for further growth studies in fish and to consider for identification of potential SNPs associated with different growth rates in response to a plant protein-based diet.
本研究的目的是测量斑马鱼中的基因表达,然后鉴定单核苷酸多态性(SNP),以用作生长关联研究中的潜在标记。我们开发了一种方法,即对从低生长和高生长的鱼中采集的肌肉样本进行RNA测序(RNA-seq)分析,并从低生长组和高生长组之间差异表达的基因中选择SNP。24个家系的鱼群从幼体到成体阶段都喂食植物蛋白基饲料。从总共440条雄鱼中,选择体重增加分布两端各5%的鱼。从8条低生长和8条高生长的鱼的个体肌肉中提取总RNA。每种表型使用4条鱼制备两个混合的RNA-Seq文库,每个文库用于一种表型。文库使用Illumina GAII测序仪进行测序,并使用CLCBio基因组工作台软件进行分析。在表型之间有124个基因差异表达(p值<0.05且错误发现率<0.2)。从这些基因中选择了164个SNP,并在240个鱼样本中进行基因分型。标记-性状分析揭示了5个与关键基因(Nars、Lmod2b、Cuzd1、Acta1b和Plac8l1)生长相关的SNP。这些基因是鱼类进一步生长研究的良好候选基因,并且可考虑用于鉴定与基于植物蛋白饮食的不同生长速率相关的潜在SNP。