National Genetic Breeding Center of Channel Catfish, Freshwater Fisheries Research Institute of Jiangsu Province, Nanjing, China.
College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China.
J Fish Biol. 2022 Oct;101(4):972-984. doi: 10.1111/jfb.15158. Epub 2022 Aug 10.
The mitogen-activated protein kinase (MAPK) gene family has been systematically described in several fish species, but less so in channel catfish (Ictalurus punctatus), which is an important global aquaculture species. In this study, 16 MAPK genes were identified in the channel catfish genome and classified into three subfamilies based on phylogenetic analysis, including six extracellular signal regulated kinase (ERK) genes, six p38-MAPK genes and four C-Jun N-terminal kinase (JNK) genes. All MAPK genes were distributed unevenly across 10 chromosomes, of which three (IpMAPK8, IpMAPK12 and IpMAPK14) underwent teleost-specific whole genome duplication during evolution. Gene expression profiles in channel catfish during salinity stress were analysed using transcriptome sequencing and qRT-PCR (quantitative reverse transcription PCR). Results from reads per kilobase million (RPKM) analysis showed IpMAPK13, IpMAPK14a and IpMAPK14b genes were differentially expressed when compared with other genes between treatment and control groups. Furthermore, three of these genes were validated by qRT-PCR, of which IpMAPK14a expression levels were significantly upregulated in treatment groups (high and low salinity) when compared with the control group, with the highest expression levels in the low salinity group (P < 0.05). Therefore, IpMAPK14a may have important response roles to salinity stress in channel catfish.
丝裂原活化蛋白激酶(MAPK)基因家族在几种鱼类中得到了系统描述,但在斑点叉尾鮰(Ictalurus punctatus)中描述较少,斑点叉尾鮰是一种重要的全球水产养殖物种。在这项研究中,在斑点叉尾鮰基因组中鉴定出了 16 个 MAPK 基因,并根据系统发育分析将其分为三个亚家族,包括六个细胞外信号调节激酶(ERK)基因、六个 p38-MAPK 基因和四个 c-Jun N 末端激酶(JNK)基因。所有 MAPK 基因在 10 条染色体上不均匀分布,其中三个(IpMAPK8、IpMAPK12 和 IpMAPK14)在进化过程中经历了硬骨鱼特异性全基因组复制。通过转录组测序和 qRT-PCR(定量逆转录 PCR)分析盐度胁迫下斑点叉尾鮰的基因表达谱。RPKM 分析结果表明,与对照组相比,IpMAPK13、IpMAPK14a 和 IpMAPK14b 基因在处理组和对照组之间的差异表达。此外,通过 qRT-PCR 验证了其中的三个基因,其中 IpMAPK14a 在处理组(高盐度和低盐度)中的表达水平与对照组相比显著上调,在低盐度组中的表达水平最高(P<0.05)。因此,IpMAPK14a 可能在斑点叉尾鮰对盐度胁迫的反应中具有重要作用。