Evaluation of reference genes for quantitative real-time PCR analysis of gene expression during early development processes of the tongue sole (Cynoglossus semilaevis)
详细信息    查看全文
  • 作者:Qian Ma ; Zhimeng Zhuang ; Wenrong Feng ; Shufang Liu…
  • 关键词:quantitative real ; time PCR ; reference gene ; early development ; Cynoglossus semilaevis
  • 刊名:Acta Oceanologica Sinica
  • 出版年:2015
  • 出版时间:October 2015
  • 年:2015
  • 卷:34
  • 期:10
  • 页码:90-97
  • 全文大小:1,043 KB
  • 参考文献:Andersen C L, Jensen J L, Orntoft T F. 2004. Normalization of realtime quantitative reverse transcription-PCR data: a modelbased variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets. Cancer Res, 64(15): 5245鈥?250CrossRef
    Aursnes A I, Rishovd A L, Karlsen E H, et al. 2011. Validation of reference genes for quantitative RT-qPCR studies of gene expression in Atlantic cod (Gadus morhua l.) during temperature stress. BMC Res Notes, 4: 104CrossRef
    Bustin S A. 2000. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. J Mol Endocrinol, 25(2): 169鈥?93CrossRef
    Bustin S A. 2002. Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems. J Mol Endocrinol, 29(1): 23鈥?9CrossRef
    Cruz F, Kalaoun S, Nobile P, et al. 2009. Evaluation of coffee reference genes for relative expression studies by quantitative realtime RT-PCR. Mol Breeding, 23(4): 607鈥?16CrossRef
    Dang Wei, Sun Li. 2011. Determination of internal controls for quantitative real time RT-PCR analysis of the effect of Edwardsiella tarda infection on gene expression in turbot (Scophthalmus maximus). Fish Shellfish Immun, 30(2): 720鈥?28CrossRef
    Deloffre L A M, Andrade A, Filipe A I, et al. 2012. Reference genes to quantify gene expression during oogenesis in a teleost fish. Gene, 506(1): 69鈥?5CrossRef
    Fernandes J M O, Mommens M, Hagen 脴, et al. 2008. Selection of suitable reference genes for real-time PCR studies of Atlantic halibut development. Comp Biochem Physiol B Biochem Mol Biol, 150(1): 23鈥?2CrossRef
    Frost P, Nilsen F. 2003. Validation of reference genes for transcription profiling in the salmon louse, Lepeophtheirus salmonis, by quantitative real-time PCR. Vet Parasitol, 118(1鈥?): 169鈥?74CrossRef
    Fu Wei, Xie Wen, Zhang Zhuo, et al. 2013. Exploring Valid reference genes for quantitative real-time PCR analysis in Plutella xylostella (Lepidoptera: Plutellidae). Int J Biol Sci, 9(8): 792鈥?02CrossRef
    Goossens K, Van Poucke M, Van Soom A, et al. 2005. Selection of reference genes for quantitative real-time PCR in bovine preimplantation embryos. BMC Dev Biol, 5(1): 27CrossRef
    Hibbeler S, Scharsack J P, Becker S. 2008. Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus. BMC Mol Biol, 9(1): 18CrossRef
    Infante C, Matsuoka M P, Asensio E, et al. 2008. Selection of housekeeping genes for gene expression studies in larvae from flatfish using real-time PCR. BMC Mol Biol, 9(1): 28CrossRef
    Ingerslev H C, Pettersen E F, Jakobsen R A, et al. 2006. Expression profiling and validation of reference gene candidates in immune relevant tissues and cells from Atlantic salmon (Salmo salar L.). Mol Immunol, 43(8): 1194鈥?201CrossRef
    Jorgensen S M, Kleveland E J, Grimholt U, et al. 2006. Validation of reference genes for real-time polymerase chain reaction studies in Atlantic salmon. Mar Biotechnol, 8(4): 398鈥?08CrossRef
    Kubista M, Andrade J M, Bengtsson M, et al. 2006. The real-time polymerase chain reaction. Mol Aspects Med, 27(2鈥?): 95鈥?25CrossRef
    Li Zhaojie, Yang Lijun, Wang Jing, et al. 2010. 尾-Actin is a useful internal control for tissue-specific gene expression studies using quantitative real-time PCR in the half-smooth tongue sole Cynoglossus semilaevis challenged with LPS or Vibrio anguillarum. Fish Shellfish Immun, 29(1): 89鈥?3CrossRef
    Liu Xuezhou, Xu Yongjiang, Ma Aijun, et al. 2004. Effects of salinity, temperature, light rhythm and light intensity on embryonic development of Cynoglossus semilaevis G眉nther and its hatching technology optimization. Mar Fish Res, 25(6): 1鈥?
    Liu Xuezhou, Zhuang Zhimeng, Ma Aajun, et al. 2005. Reproductive biology and breeding technology of Cynoglossus semilaevis. Mar Fish Res, 26(5): 7鈥?4
    Ma Qian, Liu Shufang, Zhuang Zhimeng, et al. 2011. Molecular cloning, expression analysis of insulin-like growth factor I (IGF-I) gene and IGF-I serum concentration in female and male tongue sole (Cynoglossus semilaevis). Comp Biochem Physiol B Biochem Mol Biol, 160(4): 208鈥?14CrossRef
    Ma Qian, Liu Shufang, Zhuang Zhimeng, et al. 2012. Genomic structure, polymorphism and expression analysis of the growth hormone (GH) gene in female and male Half-smooth tongue sole (Cynoglossus semilaevis). Gene, 493(1): 92鈥?04CrossRef
    McCurley A T, Callard G V. 2008. Characterization of housekeeping genes in zebrafish: male-female differences and effects of tissue type, developmental stage and chemical treatment. BMC Mol Biol, 9(1): 102CrossRef
    Mitter K, Kotoulas G, Magoulas A, et al. 2009. Evaluation of candidate reference genes for QPCR during ontogenesis and of immune- relevant tissues of European seabass (Dicentrarchus labrax). Comp Biochem Physiol B Biochem Mol Biol, 153(4): 340鈥?47CrossRef
    Olsvik P A, Lie K K, Jordal A E O, et al. 2005. Evaluation of potential reference genes in real-time RT-PCR studies of Atlantic salmon. BMC Mol Biol, 6(1): 21CrossRef
    Olsvik P A, S酶fteland L, Lie K K. 2008. Selection of reference genes for qRT-PCR examination of wild populations of Atlantic cod Gadus morhua. BMC Res Notes, 1(1): 47CrossRef
    脴verg氓rd A C, Nerland A H, Patel S. 2010. Evaluation of potential reference genes for real time RT-PCR studies in Atlantic halibut (Hippoglossus Hippoglossus L.); during development, in tissues of healthy and NNV-injected fish, and in anterior kidney leucocytes. BMC Mol Biol, 11: 36CrossRef
    Pei Desheng, Sun Yonghua, Chen Shangping, et al. 2007. Zebrafish GAPDH can be used as a reference gene for expression analysis in cross-subfamily cloned embryos. Anal Biochem, 363(2): 291鈥?93CrossRef
    Pfaffl M W, Tichopad A, Prgomet C, et al. 2004. Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper-Excel-based tool using pairwise correlations. Biotechnol Lett, 26(6): 509鈥?15CrossRef
    Radonic A, Thulke S, Mackay I M, et al. 2004. Guideline to reference gene selection for quantitative real-time PCR. Biochem Bioph Res Co, 313(4): 856鈥?62CrossRef
    Silver N, Best S, Jiang J, et al. 2006. Selection of housekeeping genes for gene expression studies in human reticulocytes using realtime PCR. BMC Mol Biol, 7(1): 33CrossRef
    Small B C, Murdock C A, Bilodeau-Bourgeois A L, et al. 2008. Stability of reference genes for real-time PCR analyses in channel catfish (Ictalurus punctatus) tissues under varying physiological conditions. Comp Biochem Physiol B Biochem Mol Biol, 151(3): 296鈥?04CrossRef
    Spanakis E. 1993. Problems related to the interpretation of autoradiographic data on gene expression using common constitutive transcripts as controls. Nucleic Acids Res, 21(16): 3809鈥?819CrossRef
    Tang Rongying, Dodd A, Lai Daniel, et al. 2007. Validation of zebrafish (Danio rerio) reference genes for quantitative realtime RT-PCR normalization. Acta Bioch Bioph Sin, 39(5): 384鈥?90CrossRef
    Thellin O, Zorzi W, Lakaye B, et al. 1999. Housekeeping genes as internal standards: use and limits. J Biotechnol, 75(2鈥?): 291鈥?95CrossRef
    Vandesompele J, De Preter K, Pattyn F, et al. 2002. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol, 3(7): RESEARCH0034CrossRef
    Wong M L, Medrano J F. 2005. Real-time PCR for mRNA quantitation. Biotechniques, 39(1): 75鈥?5CrossRef
    Zhang Zhaobin, Hu Jianying. 2007. Development and validation of endogenous reference genes for expression profiling of medaka (Oryzias latipes) exposed to endocrine disrupting chemicals by quantitative real-time RT-PCR. Toxicol Sci, 95(2): 356鈥?68CrossRef
    Zhang Baocun, Sun Li, Xiao Zhizhong, et al. 2014. Quantitative real time RT-PCR study of pathogen-induced gene expression in rock bream (Oplegnathus fasciatus): Internal controls for data normalization. Mar Genom, 15: 75鈥?4CrossRef
    Zheng Wenjiang, Sun Li. 2011. Evaluation of housekeeping genes as references for quantitative real time RT-PCR analysis of gene expression in Japanese flounder (Paralichthys olivaceus). Fish Shellfish Immun, 30(2): 638鈥?45CrossRef
    Zhong Qiwang, Zhang Quanqi, Wang Zhigang, et al. 2008. Expression profiling and validation of potential reference genes during Paralichthys olivaceus embryogenesis. Mar Biotechnol, 10(3): 310鈥?18CrossRef
  • 作者单位:Qian Ma (1)
    Zhimeng Zhuang (1)
    Wenrong Feng (1)
    Shufang Liu (1)
    Qisheng Tang (1)

    1. Key Laboratory of Sustainable Development of Marine Fisheries of Ministry of Agriculture, Shandong Provincial Key Laboratory of Fishery Resources and Eco-environment, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, 266071, China
  • 刊物主题:Oceanography; Climatology; Ecology; Engineering Fluid Dynamics; Marine & Freshwater Sciences; Environmental Chemistry;
  • 出版者:Springer Berlin Heidelberg
  • ISSN:1869-1099
文摘
Differential expression of genes is crucial to growth and development of fish. To select the appropriate genes for gene normalization during Cynoglossus semilaevis early developmental process, eight candidate reference genes (ACTB, B2M, EF1A, GADPH, RPL7, TUBA, UBCE and 18S) were tested for their adequacy by using quantitative real-time PCR. The results showed that the expression of all the examined genes exhibited tissue dependent variations in the mature C. semilaevis. EF1A was listed as the most stable reference among the 14 tissues by RefFinder. Furthermore, the recommended comprehensive ranking of the stability determined by RefFinder showed that 18S was the most stable gene during the early developmental stages (from oosphere to 90 days old) in this study. However, when divided the C t value data of the above mentioned early developmental stages into two separate periods (embryo and post-hatching periods), TUBA and 18S represented the most stable references of these two developmental periods, respectively. Consequently, the reference gene should be carefully and accurately chosen even for studies of the same species at various developmental processes. The relevant data may help in selecting appropriate reference genes for mRNA expression analysis, and is of great value in the studies of fish growth and development. Keywords quantitative real-time PCR reference gene early development Cynoglossus semilaevis

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700