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与基础的横斑洛克鸡品系相比,对单个现代肉用仔鸡雄性品系中与肌肉生长相关的全球基因表达进行RNA测序。

RNA sequencing for global gene expression associated with muscle growth in a single male modern broiler line compared to a foundational Barred Plymouth Rock chicken line.

作者信息

Kong Byung-Whi, Hudson Nicholas, Seo Dongwon, Lee Seok, Khatri Bhuwan, Lassiter Kentu, Cook Devin, Piekarski Alissa, Dridi Sami, Anthony Nicholas, Bottje Walter

机构信息

Department of Poultry Science, Center of Excellence for Poultry Science, University of Arkansas, Fayetteville, Arkansas, USA.

School of Agriculture and Food Science, University of Queensland, Gatton, Australia.

出版信息

BMC Genomics. 2017 Jan 13;18(1):82. doi: 10.1186/s12864-016-3471-y.

DOI:10.1186/s12864-016-3471-y
PMID:28086790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5237145/
Abstract

BACKGROUND

Modern broiler chickens exhibit very rapid growth and high feed efficiency compared to unselected chicken breeds. The improved production efficiency in modern broiler chickens was achieved by the intensive genetic selection for meat production. This study was designed to investigate the genetic alterations accumulated in modern broiler breeder lines during selective breeding conducted over several decades.

METHODS

To identify genes important in determining muscle growth and feed efficiency in broilers, RNA sequencing (RNAseq) was conducted with breast muscle in modern pedigree male (PeM) broilers (n = 6 per group), and with an unselected foundation broiler line (Barred Plymouth Rock; BPR). The RNAseq analysis was carried out using Ilumina Hiseq (2 x 100 bp paired end read) and raw reads were assembled with the galgal4 reference chicken genome. With normalized RPM values, genes showing >10 average read counts were chosen and genes showing <0.05 p-value and >1.3 fold change were considered as differentially expressed (DE) between PeM and BPR. DE genes were subjected to Ingenuity Pathway Analysis (IPA) for bioinformatic functional interpretation.

RESULTS

The results indicate that 2,464 DE genes were identified in the comparison between PeM and BPR. Interestingly, the expression of genes encoding mitochondrial proteins in chicken are significantly biased towards the BPR group, suggesting a lowered mitochondrial content in PeM chicken muscles compared to BPR chicken. This result is inconsistent with more slow muscle fibers bearing a lower mitochondrial content in the PeM. The molecular, cellular and physiological functions of DE genes in the comparison between PeM and BPR include organismal injury, carbohydrate metabolism, cell growth/proliferation, and skeletal muscle system development, indicating that cellular mechanisms in modern broiler lines are tightly associated with rapid growth and differential muscle fiber contents compared to the unselected BPR line. Particularly, PDGF (platelet derived growth factor) signaling and NFE2L2 (nuclear factor, erythroid 2-like 2; also known as NRF2) mediated oxidative stress response pathways appear to be activated in modern broiler compared to the foundational BPR line. Upstream and network analyses revealed that the MSTN (myostatin) -FST (follistatin) interactions and inhibition of AR (androgen receptor) were predicted to be effective regulatory factors for DE genes in modern broiler line. PRKAG3 (protein kinase, AMP-activated, gamma 3 non-catalytic subunit) and LIPE (lipase E) are predicted as core regulatory factors for myogenic development, nutrient and lipid metabolism.

CONCLUSION

The highly upregulated genes in PeM may represent phenotypes of subclinical myopathy commonly observed in the commercial broiler breast tissue, that can lead to muscle hardening, named as woody breast. By investigating global gene expression in a highly selected pedigree broiler line and a foundational breed (Barred Plymouth Rock), the results provide insight into cellular mechanisms that regulate muscle growth, fiber composition and feed efficiency.

摘要

背景

与未经选育的鸡品种相比,现代肉鸡生长速度极快且饲料效率高。现代肉鸡生产效率的提高是通过对肉类生产进行密集的遗传选择实现的。本研究旨在调查在几十年的选择性育种过程中现代肉种鸡品系中积累的基因改变。

方法

为了鉴定对肉鸡肌肉生长和饲料效率起重要作用的基因,对现代系谱雄性(PeM)肉鸡(每组n = 6)的胸肌以及未经选育的基础肉鸡品系(横斑洛克鸡;BPR)进行了RNA测序(RNAseq)。使用Illumina Hiseq(2×100 bp双端读数)进行RNAseq分析,并将原始读数与galgal4参考鸡基因组进行组装。对于标准化的RPM值,选择平均读数计数>10的基因,并将p值<0.05且变化倍数>1.3的基因视为PeM和BPR之间的差异表达(DE)基因。对DE基因进行Ingenuity通路分析(IPA)以进行生物信息学功能解释。

结果

结果表明,在PeM和BPR的比较中鉴定出2464个DE基因。有趣的是,鸡中编码线粒体蛋白的基因表达明显偏向BPR组,这表明与BPR鸡相比,PeM鸡肌肉中的线粒体含量降低。这一结果与PeM中慢肌纤维线粒体含量较低不一致。PeM和BPR比较中DE基因的分子、细胞和生理功能包括机体损伤、碳水化合物代谢、细胞生长/增殖和骨骼肌系统发育,这表明与未经选育的BPR品系相比,现代肉鸡品系中的细胞机制与快速生长和不同的肌纤维含量密切相关。特别是,与基础BPR品系相比,血小板衍生生长因子(PDGF)信号通路和核因子E2相关因子2(NFE2L2;也称为NRF2)介导的氧化应激反应通路在现代肉鸡中似乎被激活。上游和网络分析表明,肌肉生长抑制素(MSTN)-卵泡抑素(FST)相互作用以及雄激素受体(AR)的抑制被预测为现代肉鸡品系中DE基因的有效调节因子。蛋白激酶AMP激活的γ3非催化亚基(PRKAG3)和脂肪酶E(LIPE)被预测为成肌发育、营养和脂质代谢的核心调节因子。

结论

PeM中高度上调的基因可能代表了在商业肉鸡胸部组织中常见的亚临床肌病的表型,这种表型可导致肌肉硬化,即所谓的木胸。通过研究高度选育的系谱肉鸡品系和基础品种(横斑洛克鸡)中的全局基因表达,结果为调节肌肉生长、纤维组成和饲料效率的细胞机制提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/128995d8c42b/12864_2016_3471_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/a7e3c1b6ab34/12864_2016_3471_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/71f68001f322/12864_2016_3471_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/4ecc25de14f4/12864_2016_3471_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/a211606e4707/12864_2016_3471_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/128995d8c42b/12864_2016_3471_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/a7e3c1b6ab34/12864_2016_3471_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/4552daa4f779/12864_2016_3471_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/2582b99be2b4/12864_2016_3471_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/6c4e2d37eb35/12864_2016_3471_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/71f68001f322/12864_2016_3471_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/4ecc25de14f4/12864_2016_3471_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/a211606e4707/12864_2016_3471_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2b3/5237145/128995d8c42b/12864_2016_3471_Fig8_HTML.jpg

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