Zhang Genxi, Wu Pengfei, Zhou Kaizhi, He Mingliang, Zhang Xinchao, Qiu Cong, Li Tingting, Zhang Tao, Xie Kaizhou, Dai Guojun, Wang Jinyu
College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009, China.
Joint International Research Laboratory of Agriculture & Agri-Product Safety, Yangzhou University, Yangzhou, 225009, China.
BMC Genomics. 2021 Mar 6;22(1):157. doi: 10.1186/s12864-021-07453-0.
Growth performance is significant in broiler production. In the growth process of broilers, gene expression varies at different growth stages. However, limited research has been conducted on the molecular mechanisms of muscle growth and development in yellow-feathered male chickens.
In the study, we used RNA-seq to study the transcriptome of the breast muscle of male Jinghai yellow chickens at 4 (M4F), 8 (M8F) and 12 weeks (M12F) of age. The results showed that 4608 differentially expressed genes (DEGs) were obtained by comparison in pairs of the three groups with Fold Change (FC) ≥ 2 and False Discovery Rate (FDR) ≤ 0.05, and 83, 3445 and 3903 DEGs were obtained separately from M4FvsM8F, M4FvsM12F and M8FvsM12F. Six genes were found as co-differentially expressed in the three age groups, namely SNCG, MYH1A, ARHGDIB, ENSGALG00000031598, ENSGALG00000035660 and ENSGALG00000030559. The GO analysis showed that 0, 304 and 408 biological process (BP) were significantly enriched in M4FvsM8F, M4FvsM12F and M8FvsM12F groups, respectively. KEGG pathway enrichment showed that 1, 2, 4 and 4 pathways were significantly enriched in M4FvsM8F, M4FvsM12F, M8FvsM12F and all DEGs, respectively. They were steroid biosynthesis, carbon metabolism, focal adhesion, cytokine-cytokine receptor interaction, biosynthesis of amino acids and salmonella infection. We constructed short hairpin RNA (shRNA) to interfere the differentially expressed gene RAC2 in DF-1 cells and detected mRNA and protein expression of the downstream genes PAK1 and MAPK8. Results of qPCR showed that RAC2, PAK1 and MAPK8 mRNA expression significantly decreased in the shRAC2-2 group compared with the negative control (NC) group. Western Blot (WB) results showed that the proteins of RAC2, PAK1 and MAPK8 also decreased in the shRAC2-2 group. Cell Counting Kit-8 (CCK-8) and 5-Ethynyl-2'-deoxyuridine (EdU) assay both showed that the proliferation of DF-1 cells was significantly inhibited after transfection of shRAC2-2.
The results of RNA-seq revealed genes, BP terms and KEGG pathways related to growth and development of male Jinghai yellow chickens, and they would have important guiding significance to our production practice. Further research suggested that RAC2 might regulate cell proliferation by regulating PAKs/MAPK8 pathway and affect growth of chickens.
生长性能在肉鸡生产中至关重要。在肉鸡的生长过程中,基因表达在不同生长阶段会有所变化。然而,关于黄羽公鸡肌肉生长发育的分子机制的研究有限。
在本研究中,我们使用RNA测序技术研究了4周龄(M4F)、8周龄(M8F)和12周龄(M12F)的雄性京海黄鸡胸肌的转录组。结果显示,通过对三组进行两两比较,以折叠变化(FC)≥2且错误发现率(FDR)≤0.05为标准,共获得4608个差异表达基因(DEG),分别从M4FvsM8F、M4FvsM12F和M8FvsM12F中获得83个、3445个和3903个DEG。发现有6个基因在三个年龄组中共同差异表达,即SNCG、MYH1A、ARHGDIB、ENSGALG00000031598、ENSGALG00000035660和ENSGALG00000030559。基因本体(GO)分析表明,在M4FvsM8F、M4FvsM12F和M8FvsM12F组中分别有0个、304个和408个生物过程(BP)显著富集。京都基因与基因组百科全书(KEGG)通路富集显示在M4FvsM8F、M4FvsM12F、M8FvsM12F和所有DEG中分别有1条、2条、4条和4条通路显著富集;它们分别是类固醇生物合成、碳代谢、粘着斑、细胞因子-细胞因子受体相互作用、氨基酸生物合成和沙门氏菌感染。我们构建了短发夹RNA(shRNA)来干扰DF-1细胞中的差异表达基因RAC2,并检测下游基因PAK1和MAPK8 的mRNA和蛋白质表达。实时定量聚合酶链反应(qPCR)结果显示,与阴性对照(NC)组相比shRAC2-2组中RAC2、PAK1和MAPK8 mRNA表达显著降低。蛋白质免疫印迹(WB)结果显示,shRAC2-2组中RAC2、PAK1和MAPK8的蛋白质也减少。细胞计数试剂盒-8(CCK-8)和5-乙炔基-2'-脱氧尿苷(EdU)检测均显示,转染shRAC2-2后DF-1细胞的增殖受到显著抑制
RNA测序结果揭示了与雄性京海黄鸡生长发育相关的基因、BP术语和KEGG通路对我们的生产实践具有重要指导意义。进一步研究表明,RAC2可能通过调节PAKs/MAPK8通路来调节细胞增殖并影响鸡的生长。