[an error occurred while processing this directive]
Research Article

The cell cycle pathway regulates chicken abdominal fat deposition as revealed by transcriptome sequencing

Expand
  • Guangdong Key Laboratory of Agricultural Animal Genomics and Molecular Breeding, Key Lab of Chicken Genetics, Breeding and Reproduction, Ministry of Agriculture, College of Animal Science, South China Agricultural University, Guangzhou 510642, China

Received date: 2019-04-09

  Revised date: 2019-07-05

  Online published: 2019-08-26

Supported by

Supported by the National Natural Science Foundation of China No.(31702105);The China Agriculture Research System No.(CARS-41-G03);The Science and Technology Program of Guangzhou, China No.(201804020088)

Abstract

With the improvement of growth traits and feed conversion rate, the abdominal fat rate of Chinese local breeds of broilers has been increasing. Excessive abdominal fat deposition not only reduces the slaughter rate and disease resistance of broiler chickens, but also produces waste due to the difficulty of fat treatment. In order to study the regulatory genes and pathways involved in abdominal fat deposition of broilers, we used high-fat diets to feed the Xinghua Chicken, which is a Chinese local breed. Two weeks after feeding, we found that the abdominal fat weight and rate of broilers in the high-fat diet group increased significantly, and the diameter and area of abdominal fat cells also increased significantly. Transcriptome sequencing of abdominal fat and livers showed that the differentially expressed genes in the abdominal fat were mainly enriched in the cell cycle, peroxisome proliferator- activated receptor (PPAR) and extracellular matrix (ECM) receptor signaling pathways. The differentially expressed genes in livers were also significantly enriched in the cell cycle pathway, as well as in the steroid biosynthesis and PPAR signaling pathway. By analyzing the common differentially expressed genes in abdominal fat and liver tissues, we found that these genes were also enriched in cell cycle. Finally, we used the chicken LMH (chicken hepatoma cell) cell line and chicken ICP (immortalized chicken preadipocytes) cell line to do the in vitro validation assays. We used high-fat and common medium to culture the cells. The results showed that after 48 hours, the high-fat medium could significantly promote cell cycle and increase the number of cells in S phase. Additionally, qRT-PCR results showed that the high-fat medium could significantly promote the expression of genes related to cell cycle. In conclusion, we found that high-fat diets activate the cell cycle progression of chicken hepatocytes and preadipocytes, promote cell proliferation, and then increase abdominal fat deposition.

Cite this article

Jiahui Chen, Xueyi Ren, min Li, Shiyi Lu, Tian Cheng, Liangtian Tan, Shaodong Liang, Danlin He, Qingbin Luo, Qinghua Nie, Xiquan Zhang, Wen Luo . The cell cycle pathway regulates chicken abdominal fat deposition as revealed by transcriptome sequencing[J]. Hereditas(Beijing), 2019 , 41(10) : 962 -973 . DOI: 10.16288/j.yczz.19-098

References

[1] Haslam DW, James WP . Obesity. Lancet, 2005,366(9492):1197-1209.
[2] Luppino FS, de Wit LM, Bouvy PF, Stijnen T, Cuijpers P, Penninx BW, Zitman FG . Overweight, obesity, and depression: a systematic review and meta-analysis of longitudinal studies. Arch Gen Psychiat, 2010,67(3):220-229.
[3] Yan H, Zheng P, Yu B, Yu J, Mao X, He J, Huang Z, Chen D . Postnatal high-fat diet enhances ectopic fat deposition in pigs with intrauterine growth retardation. Eur J Nutr, 2017,56(2):483-490.
[4] Tu YJ, Yu DY . Study on the effects of enclosure and grazing on growth and meat quality of local chickens. China Poultry, 2004,26(19):46-47.
[4] 屠友金, 余东游 . 圈放结合对土鸡生长和肉质的影响探讨. 中国家禽, 2004, ( 19):46-47.
[5] Lang QQ . Study on the selection method of abdominal fat rate of high quality chicken[Dissertation]. South China Agricultural University, 2018.
[5] 郎倩倩 . 优质鸡腹脂率选种方法的研究[学位论文]. 华南农业大学, 2018.
[6] Abdalla BA, Chen J, Nie Q, Zhang X . Genomic insights into the multiple factors controlling abdominal fat deposition in a chicken model. Front Genet, 2018,9:262.
[7] Gong DQ, Li H, Yang S, Zhang DX, Wang QG, Yu H, Zhang HW . Selective effect of plasma VLDL concentration in broilers - body weight and plasma VLDL. Heilongjiang Anim Sci Veter Med, 1999(11):1-3.
[7] 龚道清, 李辉, 杨山, 张德祥, 王启贵, 于赫, 张宏伟 . 肉鸡血浆VLDL浓度的选择效应——肉仔鸡体重和血浆VLDL. 黑龙江畜牧兽医, 1999(11):1-3.
[8] Wijayatunga NN, Pahlavani M, Kalupahana NS, Kottapalli KR, Gunaratne PH, Coarfa C, Ramalingam L, Moustaid- Moussa N . An integrative transcriptomic approach to identify depot differences in genes and microRNAs in adipose tissues from high fat fed mice . Oncotarget, 2018,9(10):9246-9261.
[9] Livak KJ, Schmittgen TD . Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods, 2001,25(4):402-408.
[10] Nishimichi N, Aosasa M, Kawashima T, Horiuchi H, Furusawa S, Matsuda H . Biological activity of recombinant chicken interleukin-6 in chicken hybridoma cells. Vet Immunol Immunop, 2005,106(1-2):97-105.
[11] Wang W, Zhang T, Wu C, Wang S, Wang Y, Li H, Wang N . Immortalization of chicken preadipocytes by retroviral transduction of chicken TERT and TR. PLoS One, 2017,12(5):e0177348.
[12] Li DD . Study on the mechanism of targeted regulation of Dvl2 on BMSCs osteogenic differentiation by microRNA- 29c-3p in high-fat environment [Dissertation]. Shandong University, 2017.
[12] 李多多 . 高脂环境下miR-29c-3p靶向调节Dvl2对BMSCs成骨分化机制研究[学位
Outlines

/