QPCTL Affects the Daily Weight Gain of the F2 Population and Regulates Myogenic Cell Proliferation and Differentiation in Chickens
文献类型: 外文期刊
作者: Ren, Tuanhui 1 ; Lin, Wujian 1 ; Yang, Xiuxian 1 ; Zhang, Zihao 1 ; He, Shizi 1 ; Li, Wangyu 1 ; Li, Zhuanjian 4 ; Zhang, Xiquan 1 ;
作者机构: 1.South China Agr Univ, Coll Anim Sci, Dept Anim Genet Breeding & Reprod, Guangzhou 510642, Peoples R China
2.Guangdong Prov Key Lab Agroanim Genom & Mol Breedi, Guangzhou 510642, Peoples R China
3.Minist Agr, Key Lab Chicken Genet Breeding & Reprod, Guangzhou 510642, Peoples R China
4.Henan Agr Univ, Coll Anim Sci & Technol, Zhengzhou 450046, Peoples R China
关键词: QPCTL; Indel; daily weight gain; primary myoblast; cell proliferation
期刊名称:ANIMALS ( 影响因子:3.231; 五年影响因子:3.312 )
ISSN: 2076-2615
年卷期: 2022 年 12 卷 24 期
页码:
收录情况: SCI
摘要: Simple Summary Molecular breeding can accelerate the process of animal breeding and improve breeding efficiency. At present, many Indel molecular markers have been identified in livestock and poultry, but how Indels affect economic traits is not well understood. For molecular breeding, it is crucial to reveal the mechanism of action of Indels and to provide more accurate information. The purpose of this study was to investigate how the 52/224-bp multiallelic Indels of the chicken QPCTL promoter area affect the daily weight gain of chickens and the potential regulatory mechanism of the QPCTL gene. The analysis was conducted by association analysis, qPCR, dual-fluorescence assay and Western blotting. The results of this study suggest that Indels in the promoter region of the QPCTL gene may regulate the proliferation and differentiation of chicken primary myoblasts by affecting the expression of QPCTL, which ultimately affects the growth rate of chickens. These Indels have important value for the molecular breeding of chickens, and QPCTL can be used as a candidate gene to regulate and improve chicken growth and development. Molecular breeding can accelerate the process of animal breeding and improve the breeding efficiency. To date, many Indel molecular markers have been identified in livestock and poultry, but how Indels affect economic traits is not well understood. For molecular breeding, it is crucial to reveal the mechanism of action of Indels and to provide more accurate information. The purpose of this study was to investigate how the 52/224-bp multiallelic Indels of the chicken QPCTL promoter area affect the daily weight gain of chickens and the potential regulatory mechanism of the QPCTL gene. The analysis was conducted by association analysis, qPCR, dual-fluorescence assay and Western blotting. The results showed that Indels in the QPCTL promoter region were significantly associated with the daily weight gain in chickens and that QPCTL expression showed a decreasing trend in embryonic breast muscle tissues. Furthermore, QPCTL expression was significantly higher in breast muscle tissues of the AC genotype than in those of the AB and BB genotypes. Based on the transcriptional activity results, the pGL3-C vector produced more luciferase activity than pGL3-A and pGL3-B. In addition, overexpression of QPCTL promoted chicken primary myoblast (CPM) proliferation and inhibited differentiation. The results of this study suggest that Indels in the promoter region of the QPCTL gene may regulate the proliferation and differentiation of CPMs by affecting the expression of QPCTL, which ultimately affects the growth rate of chickens. These Indels have important value for the molecular breeding of chickens, and QPCTL can be used as a candidate gene to regulate and improve chicken growth and development.
- 相关文献
作者其他论文 更多>>
-
Application of mRNA-Seq and Metagenomic Sequencing to Study Salmonella pullorum Infections in Chickens
作者:Chao, Xiaohuan;Fan, Zhexia;Wu, Jiongwen;Ye, Chutian;Wang, Xiaomeng;Li, Ruina;Chen, Shuya;Zhang, Xiquan;Fang, Cheng;Luo, Qingbin;Fan, Zhexia;Wu, Jiongwen;Ye, Chutian;Wang, Xiaomeng;Li, Ruina;Chen, Shuya;Zhang, Xiquan;Fang, Cheng;Luo, Qingbin
关键词:
Salmonella pullorum ; chicken; DEGs; DEASs; microbial community -
EGR1 mRNA expression levels and polymorphisms are associated with slaughter performance in chickens
作者:Ye, Mao;Ye, Chutian;Guo, Lijin;Fan, Zhexia;Ma, Xuerong;Liu, Aijun;Liang, Weiming;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Ye, Mao;Chao, Xiaohuan;Ye, Chutian;Guo, Lijin;Fan, Zhexia;Ma, Xuerong;Liu, Aijun;Liang, Weiming;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Ye, Mao;Chao, Xiaohuan;Ye, Chutian;Guo, Lijin;Fan, Zhexia;Ma, Xuerong;Liu, Aijun;Liang, Weiming;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Ye, Mao;Chao, Xiaohuan;Ye, Chutian;Guo, Lijin;Fan, Zhexia;Ma, Xuerong;Liu, Aijun;Liang, Weiming;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin
关键词:Early growth response protein 1 ( EGR1 ); Polymorphism; Slaughter performance; Association analysis; Skeletal muscle
-
METTL3-dependent m6A modification of GHR mRNA regulates mitochondrial function through mitochondrial biogenesis during myoblast differentiation
作者:Zhao, Changbin;Hu, Bowen;Wang, Zhijun;Zhang, Ze;Luo, Wen;Li, Hongmei;Zhang, Xiquan;Zhao, Changbin;Hu, Bowen;Wang, Zhijun;Zhang, Ze;Luo, Wen;Li, Hongmei;Zhang, Xiquan;Zhao, Changbin;Hu, Bowen;Wang, Zhijun;Zhang, Ze;Luo, Wen;Li, Hongmei;Zhang, Xiquan
关键词:GHR; METTL3; m6A; Mitochondrial biogenesis; Mitochondrial function
-
Heat Stress Influences Immunity Through DUSP1 and HSPA5 Mediated Antigen Presentation in Chickens
作者:Wang, Xiaomeng;Chao, Xiaohuan;Zhang, Wenwu;Zhang, Xiquan;Wu, Jiongwen;Ye, Chutian;Ma, Xuerong;Fan, Zhexia;Liu, Manqing;Fang, Cheng;Luo, Qingbin;Wang, Xiaomeng;Zhang, Wenwu;Zhang, Xiquan;Wu, Jiongwen;Ye, Chutian;Ma, Xuerong;Fan, Zhexia;Liu, Manqing;Fang, Cheng;Luo, Qingbin
关键词:chicken; immune response; mRNA-seq;
DUSP1 ;HSPA5 -
Genetic regulation of gene expression across multiple tissues in chickens
作者:Guan, Dailu;Wang, Ying;Zhou, Huaijun;Bai, Zhonghao;Zhu, Di;Li, Houcheng;Buitenhuis, Albert Johannes;Sahana, Goutam;Lund, Mogens Sando;Fang, Lingzhao;Zhu, Xiaoning;Zhu, Di;Wang, Yuzhe;Hu, Xiaoxiang;Zhong, Conghao;Lan, Fangren;Li, Xiaochang;Sun, Congjiao;Yang, Ning;Zhong, Conghao;Lan, Fangren;Li, Xiaochang;Sun, Congjiao;Yang, Ning;Hou, Yali;Pan, Zhangyuan;Si, Wei;Diao, Shuqi;Gao, Yahui;Teng, Jinyan;Xu, Zhiting;Lin, Qing;Li, Zhenhui;Nie, Qinghua;Zhang, Xiquan;Zhang, Zhe;Yao, Yuelin;Yao, Yuelin;Zhao, Bingru;Gao, Yahui;Liu, George E.;Gao, Yahui;Zou, Dong;Wang, Ruizhen;Xu, Tianyi;Zhang, Zhang;Zou, Dong;Wang, Ruizhen;Xu, Tianyi;Zhang, Zhang;Wang, Ruizhen;Zhang, Zhang;Yin, Hongwei;Shi, Shourong;Shao, Dan;Degalez, Fabien;Lagarrigue, Sandrine;Wang, Mingshan;Peng, Minsheng;Wang, Mingshan;Peng, Minsheng;Rocha, Dominique;Charles, Mathieu;Smith, Jacqueline;Watson, Kellie;Warren, Wesley;Frantz, Laurent;Frantz, Laurent;Larson, Greger;Lamont, Susan J.;Si, Wei;Zhao, Xin;Li, Bingjie;Zhang, Haihan;Luo, Chenglong;Shu, Dingming;Qu, Hao;Luo, Wei;Li, Zhenhui;Nie, Qinghua;Zhang, Xiquan;Li, Zhenhui;Nie, Qinghua;Zhang, Xiquan;Xiang, Ruidong;Xiang, Ruidong;Xiang, Ruidong;Liu, Shuli;Cheng, Hans
关键词:
-
16S rDNA sequencing combined with metabolomic probes to investigate the effects of Salmonella Pullorum on gut microbes and metabolites in broilers
作者:Wu, Jiongwen;Xue, Ruixiang;Fan, Zhexia;Li, Ruina;Wang, Xiaomeng;Ye, Chutian;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Wu, Jiongwen;Xue, Ruixiang;Fan, Zhexia;Li, Ruina;Wang, Xiaomeng;Ye, Chutian;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Wu, Jiongwen;Xue, Ruixiang;Fan, Zhexia;Li, Ruina;Wang, Xiaomeng;Ye, Chutian;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Wu, Jiongwen;Xue, Ruixiang;Fan, Zhexia;Li, Ruina;Wang, Xiaomeng;Ye, Chutian;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin
关键词:pullorum disease; Salmonella pullorum; cecum; metabolites; microorganisms
-
Joint analysis of whole-genome methylation and transcriptome in avian pullorum disease and validation of gene function
作者:Wu, Jiongwen;Liang, Weiming;Liu, Aijun;Wang, Xiaomeng;Fan, Zhexia;Ma, Xuerong;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin;Wu, Jiongwen;Liang, Weiming;Liu, Aijun;Wang, Xiaomeng;Fan, Zhexia;Ma, Xuerong;Chen, Shuya;Fang, Cheng;Zhang, Xiquan;Luo, Qingbin
关键词:Pullorum disease; Salmonella pullorum; Whole-genome bisulfite sequencing; Transcriptomics; Immune regulation



