期刊文献+

miR-26b和miR-224在梅山与杜洛克猪卵泡中的差异表达分析 被引量:3

Differential Expression Analysis of miR-26b and miR-224 in Ovarian Follicles of Meishan and Duroc Sows
下载PDF
导出
摘要 为了探讨miRNAs在猪卵泡和繁殖相关组织中的表达,采用荧光定量RT-PCR法和组织表达谱分析法,对miR-26b和miR-224在梅山和杜洛克猪卵泡及其他繁殖相关组织中的表达进行了研究。组织表达谱分析结果表明:miR-26b和miR-224在下丘脑、垂体、子宫、输卵管、卵巢、子宫角、黄体组织中均有表达。RT-PCR结果表明:miR-26b在L卵泡中的表达量梅山猪是杜洛克猪的2倍(P<0.01);而在S卵泡中的表达量杜洛克是梅山猪的10倍(P<0.01);两品种在M1和M2卵泡中的表达量差异不显著。miR-224在S卵泡中的表达量杜洛克是梅山的7.79倍(P<0.01);而在M2卵泡中表达量梅山是杜洛克的1.84倍(P<0.05);两品种在M1和L卵泡中的表达量差异不显著。在猪种内大卵泡L、中等卵泡M2、中等卵泡M1、小卵泡S的相对表达量也有不同程度的差异。此研究表明,miR-26b和miR-224在梅山和杜洛克猪中表达趋势相似,它们的表达差异可能影响卵泡发育和成熟,为深入了解miR-26b和miR-224在卵泡发育中的作用奠定了基础。 To explore the expression of miR-26b and miR-224 in ovarian follicles and reproduction-related tissues of Duroc and Meishan Sows,quantitative Real-time RT-PCR (qRT-PCR) technique was used in this study. The results showed that miR-26b and miR-224 were both expressed in hypothalamus,hypophysis,uterus,cornua uteri,ovary,oviduct and corpus luteum.The qRT-PCR results indicated that miR-26b and miR-224 were differentially expressed in follicles of different size and breed.For miR-26b,the relative expression amount in follicle L of Meishan was twice of that in Duroc, however,the expression amount in follicle S Duroc was ten times of that in Meishan.For miR-224,the relative expression amount in follicle S Duroc was 7.79 times of that in Meishan, but the expression amount in follicle M2 Meishan was 1.84 times of that in Duroc.These different expression patterns of miR-26b and miR-224 in the follicle of Meishan and Duroc maybe affect the development and maturation of follicles. Our research will be useful for further study on the molecular mechanism of ovulation regulatory network.
出处 《石河子大学学报(自然科学版)》 CAS 2014年第2期164-168,共5页 Journal of Shihezi University(Natural Science)
基金 国家自然科学基金项目(31060295)
关键词 miR-26b miR-224 卵泡 梅山猪 杜洛克猪 miR-26b miR-224 follicle Meishan Duro
  • 相关文献

参考文献20

  • 1Tol0ubeydokhti T,Bukulmez O,Chegini N,et al.Potential regulatory functions of microRNAs in the ovary [J].Semin Reprod Med,2008,26(6):469-478.
  • 2Sirotkin A V,Ovcharenko D,Grossmann R,et al.Identifica- tion of microRNAs controlling human ovarian cell steroidogenesis via a genome-scale screen[J].J Cell Phys- iol,2009,219(2):415 -420.
  • 3Yao N,Lu C L,Zhao J J,et al.A network of miRNAs ex- pressed in the ovary are regulated by FSH[J].Front Biosci, 2009,14:3239-3245.
  • 4Nagaraja A K,Andreu Vieyra C,Franco H L,et al.Deletion of Dicer in somatic cells of the female reproductive tract caus- es sterility[J].Mol Endocrinol,2008,22(10): 2336-2352.
  • 5Otsuka M,Zheng M,Hayashi M,et al.Impaired microRNA processing causes corpus luteum insufficiency and infer tility in mice[J].J Clin Invest.2008,118(5): 1944-54.
  • 6Jinju Han,Ahmet M Denli,Fred H Gage,et al.The ene- my within:intronic miR-26b represses its host gene,ctd- sp2,to regulate neurogenesis[J].Genes Dev,2012,26(1):6- 10.
  • 7Ying Zhu,Yang Lu,Qi Zhang,et al.MicroRNA-26a/b and their host genes cooperate to inhibit the G1/S transi- tion by activating the pRb protein [J].Nucleic Acids Res,2012,40(10):4615-4625.
  • 8Fei Lin,Ran Li,Zeng Xiang Pan,et al.miR-26b promotes granulosa cell apoptosis by targeting ATM during follicu- lax atresia in porcine ovaxy[J].PLoS One,2012,7(6):e38640.
  • 9Yu Wang,Jianwei Ren,Yun Gao,et al.MicroRNA-224 targets SMAD family member 4 to promote cell prolif- eration and negatively influence patient survival[J].PLoS One,2013,8(7):e68744.
  • 10Yao G,Liang M,Liang N,et al.MicroRNA-224 is involved in the regulation of mouse cumulus expansion by targeting Ptx3[J].Mol Cell Endocrinol,2014,382(l):244-253.

二级参考文献72

  • 1程宁辉,杨金水,高燕萍,徐明良,钱旻,葛扣麟.玉米杂种一代与亲本基因表达差异的初步研究[J].科学通报,1996,41(5):451-454. 被引量:91
  • 2Engels B M,Hutvagner G.Principles and effects of microRNA mediated post-transcrip tional gene regulation[J].Oncogene,2006,25(46):6163-6169.
  • 3Shi X B,Xue L,Rang J,et al.An androgen regulated miRNA suppresses Bakl ex pression and induces androgen-independent growth of prostate cancer cells[J].Proc Nan Acad Sci USA,2007,104(50):19983-19988.
  • 4Bueno M J,Perez de Castro I,Gomez de,et al.Genetic and epigenetic silencing of microRNA-203 enhances ABL1 and BCR-ABL1 oncogene expression[J].Cancer Cell 2008,13(6):496-506.
  • 5Davis E,Caiment F,Tordoir X,et al.RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus[J].Curr Biol,2005,15 (7):743-749.
  • 6Melendez B,Cuadros M,Robledo M,et al.Coincidental LOH regions in mouse and humans:evidence for novel tumor suppresor loci at 9q22-q34 in non-Hodgkin' s lymphomas[J].Leuk Res,2003,27 (8):627-633.
  • 7Feber A,Xi L,Luketich J D,et al.MicroRNA expression profiles of esophageal cancer[J].J Thorac Cardiovasc Surg,2008,135(2):255-260.
  • 8Mathe E A,Nguyen G H,Bowman E D,et al.MicroRNA expression in squamous cell carcinoma and adenocarcinoma of the esophagus:associations with survival[J].Clin Cancer Res,2009,15 (19):6192-6200.
  • 9Viticchie G,Lena A M,Latina A,et al.MiR-203 controls proliferation,migration and invasive potential of prostate cancer cell lines[J].Cell Cycle,2011,10 (7):15-19.
  • 10Li J,Chen Y,Zhao J,et al.MiR-203 reverses chemoresistance in p53-mutated colon cancer cells[J].Cancer Lett,2011,304(1):52-59.

共引文献9

同被引文献24

引证文献3

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部