研究报告

乏情和发情初产母猪下丘脑-垂体-卵巢轴中lincRNAs表达谱比较分析

展开
  • 1. 河南省农业科学院畜牧兽医研究所,河南省畜禽繁育与营养调控重点实验室,郑州 450002
    2. 河南花花牛实业总公司,郑州 450000
任巧玲,硕士,副研究员,研究方向:猪的育种与营养。E-mail: renql76@163.com;

收稿日期: 2019-11-14

  修回日期: 2020-02-29

  网络出版日期: 2020-03-26

基金资助

河南省农业科学院科技创新创意项目编号(2020CX06);河南省重点研发专项编号(182102110063);河南省财政预算科研专项项目编号(2019CY015);河南省农业科学院自主创新项目资助编号(2019ZC42)

Comparison and analysis of lincRNAs expression profile in the hypothalamic-pituitary-ovarian axis of anestrous and estrous primiparous sows

Expand
  • 1. Henan Key Laboratory of Farm Animal Breeding and Nutritional Regulation , Institute of Animal Husbandry and Veterinary Science, Henan Academy of Agricultural Sciences, Zhengzhou 450002,China
    2. Henan Huahuaniu Industrial Corporation, Zhengzhou 450000, China

Received date: 2019-11-14

  Revised date: 2020-02-29

  Online published: 2020-03-26

Supported by

Supported by Science and Technology Innovation Program No(2020CX06);Key Special Rresearch and Development Program of Henan Province No(182102110063);Henan Province Financial Budget for Scientific Research Program No(2019CY015);the Program for Independent Innovative Research in Henan Academy of Agricultural Sciences No(2019ZC42)

摘要

初产母猪断奶后能否正常发情对养猪生产影响重大,也是初产母猪被淘汰的主要原因。本研究以乏情和发情初产母猪为研究对象,首次利用RNA-seq技术对其下丘脑-垂体-卵巢轴中的基因间长链非编码RNAs(long intergenic noncoding RNAs, lincRNAs)进行筛选比较,得到lincRNAs的表达图谱,并对其特征和功能进行了初步分析。结果显示,在乏情和发情初产母猪下丘脑-垂体-卵巢轴中鉴定得到3519个lincRNAs,以发情组为对照共有17个lincRNAs存在差异表达,其中12个表达上调,5个表达下调(FC≥2, P<0.05)。选择4个差异表达的lincRNAs经qRT-PCR验证,其表达水平与测序结果基本一致。对这17个差异表达的lincRNAs进行GO分析、KEGG通路分析及lincRNA-mRNA共表达网络分析,发现这些lincRNAs主要与猪卵母细胞减数分裂成熟、卵巢细胞分化及颗粒细胞凋亡等生殖活动相关。本研究结果丰富了猪lincRNAs数据资源,为进一步深入研究初产母猪的生殖机能提供了理论依据。

本文引用格式

任巧玲, 张家庆, 陆东锋, 王璟, 陈俊峰, 马强, 白献晓, 郭红霞, 高彬文, 邢宝松 . 乏情和发情初产母猪下丘脑-垂体-卵巢轴中lincRNAs表达谱比较分析[J]. 遗传, 2020 , 42(4) : 388 -402 . DOI: 10.16288/j.yczz.19-347

Abstract

The normal estrus in weaned primiparous sows has a great impact on pig production and abnormal estrus is the main reason for the elimination of primiparous sows. In this study, we studied the long intergenic noncoding RNAs (lincRNAs) in the hypothalamic-pituitary-ovarian axis of anestrous and estrous primiparous sows. These long intergenic noncoding RNAs (lincRNAs) were screened and compared through RNA-seq analysis. The expression profiles of lincRNAs were obtained and their characteristics and functions were preliminarily analyzed. There are 3519 novel lincRNAs identified in the hypothalamic-pituitary-ovarian axis of anestrous and estrous primiparous sows. Compared with estrous primiparous sows, 17 differentially expressed lincRNAs were indentified, including 12 up-regulated lincRNAs and 5 down-regulated lincRNAs (FC≥2, P<0.05). The four lincRNA transcripts obtained through selection were verified by qRT-PCR, which are consistent with the RNA-seq results. The GO, KEGG pathway, and lincRNA-mRNA co-expression network analysis of these 17 lincRNAs revealed that these lincRNAs were mainly involved in reproductive activities, such as oocyte meiosis mature, ovarian cells differentiation and granulosa cells apoptosis. The results enriched the data resources of pig lincRNAs and provided useful information for further research about the reproductive performance of primiparous sows.

参考文献

[1] Zhou DS, Zhuo Y, Che LQ, Lin Y, Fang ZF, Wu D . Nutrient restriction induces failure of reproductive function and molecular changes in hypothalamus-pituitary-gonadal axis in postpubertal gilts. Mol Biol Rep, 2014,41(7):4733-4742.
[2] Kong LJ, Wang AG, Fu JL, Lai CH, Wang XF, Lin HC . Peroxisome proliferator-activated recptor γ is involved in weaning to estrus of primiparous sows by regulating the expression of hormone genes in hypothalamus-pituitary- ovary axis. Asian-Aust J Anim Sci, 2007,20(3):340-350.
[3] Topaloglu AK, Reimann F, Guclu M, Yalin AS, Kotan LD, Porter KM, Serin A, Mungan NO, Cook JS, Ozbek MN, Imamoglu S, Akalin NS, Yuksel B, Rahily SO , Semple RK . TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction. Nat Genet, 2009,41(3):354-358.
[4] Lehman MN, Coolen LM, Goodman RL . Minireview: Kisspeptin/neurokinin B/dynorphin (KNDy) cells of the arcuate nucleus: A central node in the control of Gonadotropin-Releasing hormone secretion. Endocrinology, 2010,151(8):3479-3489.
[5] Song S, Cui P, Wang YY, Jiang SD, Zhang XR, Fang FG, Li SB . Expression of neurokinin B in hypothalamus, pituitary and ovary of rats. J Northwest Sci-Tech Univ Agric Fore(Nat Sci Ed), 2015,43(6):7-14, 20.
[5] 宋爽, 崔培, 王尧尧, 蒋书东, 章孝荣, 方富贵, 李书宝 . 神经激肽B在大鼠下丘脑-垂体-卵巢轴上的表达. 西北农林科技大学(自然科学版), 2015,43(6):7-14, 20.
[6] Ulitsky I, Bartel DP . LincRNAs: genomics, evolution, and mechanisms. Cell, 2013,154(1):26-46.
[7] Popadin K, Gutierrez-Arcelus M, Dermitzakis ET, Antonarakis SE . Genetic and epigenetic regulation of human lincRNA gene expression. AM J Hum Genet, 2013,93(6):1015-1026.
[8] Guttman M, Donaghey J, Carey BW, Garber M, Grenier JK, Munson G, Young G, Lucas AB, Ach R, Bruhn L, Yang XP, Amit I, Meissner A, Regev A, Regev A, Rinn JL, Root DE, Lander ES . LincRNAs act in the circuitry controlling pluripotency and differentiation. Nature, 2012,477(7364):295-300.
[9] Augui S, Nora EP, Heard E . Regulation of X-chromosome inactivation by the X-inactivation centre. Nat Rev Genet, 2011,12(6):429-442.
[10] Li JY, Gao ZL, Wang XY, Liu HB, Zhang Y, Liu ZH . Identification and functional analysis of long intergenic noncoding RNA genes in porcine pre-implantation embryonic development. Sci Rep, 2016,6:38333.
[11] Muys BR, Lorenzi JCC, Zanette DL, Bueno RdBLe, Araújo LFd, Dinarte-Santos AR, Alves CP, Ram?o A, Molfetta GAd, Vidal DO, Silva WA Jr . Placenta-enriched LincRNAs MIR503HG and LINC00629 decrease migration and invasion potential of JEG-3 cell line. PLoS One, 2016,11(3):e0151560.
[12] Amin V, Harris RA, Onuchic V, Jackson AR, Charnecki T, Paithankar S, Lakshmi Subramanian SL, Riehle K, Coarfa C, Milosavljevic A . Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAs. Nat Commun, 2015,6:6370-6380.
[13] Zhou C, Li S, Deng LL, Guan Y, Chen DK, Yuan XK, Xia TR, He XL, Shan YW, Li CC . Transcriptome analysis reveals long intergenic noncoding RNAs contributed to growth and meat quality differences between yorkshire and wannanhua pig. Genes, 2017,8(8):E203.
[14] Zhao YH . Identification and functional analysis of lincRNA based on multi-tissue transcriptome data in mice[Dissertation] . Beijing Institute of Genomics, Chinese Academy of Sciences, 2015.
[14] 赵宇慧 . 基于多组织转录组数据的小鼠lincRNA的鉴定和功能分析[学位论文]. 中国科学院北京基因组研究所, 2015.
[15] Tang ZL, Wu Y, Yang YL, Yang YCT, Wang ZS, Yuan JP, Yang Y, Hua CJ, Fan XH, Niu GG, Zhang YB, Lu ZJ, Li K . Comprehensive analysis of long non-coding RNAs highlights their spatio-temporal expression patterns and evolutional conservation in Sus scrofa. Sci Rep, 2017,7:43166.
[16] Li JY, Gao ZL, Wang XY, Liu HB, Zhang Y, Liu ZH . Identification and functional analysis of long intergenic noncoding RNA genes in porcine pre-implantation embryonic development. Sci Rep, 2016,6:38333.
[17] Liu KS, Li TP, Ton H, Mao XD, Chen YJ . Advances of long noncoding RNAs-mediated regulation in reproduction. Chin Med J(Engl), 2018,131(2):226-234.
[18] Muys BR, Lorenzi JCC, Zanette DL, De Barros Lima E Bueno R, De Araujo LF, Dinarte-Santos AR, Alves CP, Ramao A, De Molfetta GA, Vidal DO, Silva WA, . Placenta-enriched LincRNAs MIR503HG and LINC00629 decrease migration and invasion potential of JEG-3 cell line. PLoS One, 2016,11(3):e0151560.
[19] Cabili MN, Trapnell C, Goff L, Koziol M, Tazon-Vega B, Regev A, Rinn JL . Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev, 2011,25(18):1915-1927.
[20] Lv J, Liu H, Yu SH, Liu HB, Cui W, Gao Y, Zheng T, Qin G, Guo J, Zeng TB, Han ZB, Zhang Y, Wu Q . Identification of 4438 novel lincRNAs involved in mouse pre-implantation embryonic development. Mol Gen Genomics, 2015,290(2):685-697.
[21] Zhang JY, Lv S, Niu HM, Lei AM . Research progress on the asymmetric division in mammalian oocytes. Hereditas (Beijing), 2018,40(4):279-291.
[21] 张俊玉, 吕珊, 牛慧敏, 雷安民 . 哺乳动物卵母细胞不对称分裂的研究进展. 遗传, 2018,40(4):279-291.
[22] Zhu XL, Qi ST, Liu J, Chen L, Zhang C, Yang SW, OuYang YC, Hou Y, Schatten H, Song YL, Xing FQ, Sun QY . Synaptotagmin1 is required for spindle stability and metaphase-to-anaphase transition in mouse oocytes. Cell Cycle, 2012,11(4):818-826.
[23] Solc P, Schultz RM, Motlik J . Prophase I arrest and progression to metaphase I in mouse oocytes: comparison of resumption of meiosis and recovery from G2-arrest in somatic cells. Mol Hum Reprod, 2010,16(9):654-664.
[24] Yang F, Zhang BY, Feng GD, Xiang W, Ma YX, Chen H, Chu MX, Wang PQ . A Mechanistic review of how hypoxic mircroenvironment regulates mammalian ovulation. Hereditas(Beijing), 2016,38(2):109-117.
[24] 杨芳, 张宝云, 冯光德, 向伟, 马云霞, 陈航, 储明星, 王凭青 . 卵巢低氧微环境调节哺乳动物排卵的分子机制. 遗传, 2016,38(2):109-117.
[25] Nanassy L, Lee K, Javor A, Machaty Z . 316 Changes in MPF activity in porcine oocytes following activation by various methods. Reprod Fert Develop, 2006,18(2):265-265.
[26] Faerge I, Terry B, Kalous J, Wahl P, Lessl M, Ottesen JL, Hyttel P, Gr?ndahl C . Resumption of meiosis induced by meiosis-activating sterol has a different signal transduction pathway than spontaneous resumption of meiosis in denuded mouse oocytes cultured in vitro. Biol Reprod, 2001,65(6):1751-1758.
[27] Zhang DX, Park WJ, Sun SC, Xu YN, Li YH, Cui XS, Kim NH . Regulation of maternal gene expression by MEK/MAPK and MPF signaling in porcine oocytes during in vitro meiotic maturation. J Reprod Dev, 2011,57(1):48-56.
[28] Zhang DX, Cui XS, Kim NH . Molecular characterization and polyadenylation-regulated expression of cyclin B1 and Cdc2 in porcine oocytes and early parthenotes. Mol Reprod Dev, 2010,77(1):38-50.
[29] Liang CG, Su YQ, Fan HY, Schatten H, Sun QY . Mechanisms regulating oocyte meiotic resumption: roles of mitogen-activated protein kinase. Mol Endocrinol, 2007,21(9):2037-2055.
[30] Lee SE, Kim JH, Kim NH . Inactivation of MAPK affects centrosome assembly, but not actin filament assembly, in mouse oocytes maturing in vitro. Mol Reprod Dev, 2007,74(7):904-911.
[31] Lee J, Miyano T, Moor RM . Localisation of phosphorylated MAP kinase during the transition from meiosis I to meiosis II in pig oocytes. Zygote, 2000,8(2):119-125.
[32] Lan W, Petznick A, Heryati S, Rifada M, Tong L . Nuclear factor-κB: central regulator in ocular surface inflammation and diseases. Ocul Surf, 2012,10(3):137-148.
[33] Siomek A . NF-κB signaling pathway and free radical impact. Acta Biochim Pol, 2012,59(3):323-331.
[34] Wullaert A, Bonnet MC, Pasparakis M . NF-κB in the regulation of epithelial homeostasis and inflammation. Cell Res, 2011,21(1):146-158.
[35] Ling XQ, Wang JK . Techniques for assaying the activity of transcription factor NF-κB. Hereditas (Beijing), 2013,35(5):551-570.
[35] 凌小倩, 王进科 . 转录因子NF-κB活性检测技术. 遗传, 2013,35(5):551-570.
[36] Campbell KJ, Rocha S, Perkins ND . Active repression of antiapoptotic gene expression by RelA(p65) NF-kappa B. Mol Cell, 2004,13(6):853-865.
[37] Ma JJ, Ren ZJ, Ma Y, Xu L, Zhao Y, Zheng CG, Fang YH, Xue T, Sun BL, Xiao WH . Targeted knockdown of EGR-1 inhibits IL-8 production and IL-8-mediated invasion of prostate cancer cells through suppressing EGR-1/NF-κB synergy. J Biol Chem, 2009,284(50):34600-34606.
[38] Pavlová S, Klucska K, Va?í?ek D, Ryban L, Harrath AH, Alwasel SH, Sivotkin AV, . The involvement of SIRT1 and transcription factor NF-κB (p50/p65) in regulation of porcine ovarian cell function. Anim Reprod Sci, 2013,140(3-4):180-188.
[39] Sirotkin AV, Dekanová P, Harrath AH, Alwasel SH, Va?í?ek D, . Interrelationships between sirtuin1 and transcription factors P53 and NF-κB(P50/P65) in the control of ovarian cell apoptosis and proliferation. Cell Tissue Res, 2014,358(4):627-632.
[40] Cai HQ, Zhang YY, Pypaert M, Walker L, Ferro-Novick S . Mutants in trs120 disrupt traffic from the early endosome to the late Golgi. J Cell Biol, 2005,171(5):823-833.
[41] Hu WH, Pendergast JS, Mo XM, Brambilla R, Bracchi- Ricard V, Li F, Walters WM, Blits B, He L, Shaal SM, Bethea JR . NIBP, a novel NIK and IKKβ-binding protein that enhances NF-κB activation. J Biol Chem, 2005,280(32):29233-29241.
[42] Balboula AZ, Stein P, Schultz RM, Schindler K . Knockdown of RBBP7 unveils a requirement of histone deacetylation for CPC function in mouse oocytes. Cell Cycle, 2014,13(4):600-611.
[43] Balboula AZ, Stein P, Schultz RM, Schindler K . RBBP4 regulates histone deacetylation and bipolar spindle assembly during oocyte maturation in the mouse. Biol Reprod, 2015,92(4):105-117.
文章导航

/