Validation of reference genes for quantitative real-time PCR during Chinese wolfberry fruit development

被引:27
作者
Wang, Lijuan [1 ]
Wang, Yancai [1 ]
Zhou, Ping [1 ]
机构
[1] Ningxia Univ, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
Quantitative real-time reverse transcription; PCR; Lycium barbarum L; Reference genes; Validation; Fruit development; POLYMERASE-CHAIN-REACTION; RT-PCR; INTERNAL CONTROL; SYSTEMATIC VALIDATION; HOUSEKEEPING GENES; EXPRESSION; NORMALIZATION; IDENTIFICATION; QUANTIFICATION; SELECTION;
D O I
10.1016/j.plaphy.2013.05.038
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Lycium barbarum L., a woody bush that grows in Eurasia and North Africa, is an ornamental and medicinal plant. Its fruits have been used for centuries in China as a traditional herbal medicine and as a valuable nourishing tonic. There has been no report describing the selection of reference genes for stringent normalization for quantitative PCR (qPCR) in L. barbarum. The present study identified reliable reference genes for normalization of qPCR data in L barbarum during fruit development from among eight candidate genes (GAPDH, TEF G, EF 1a, UBQ, TUB a, SAMS, EF2 and Hsp80) using the geNorm and NormFinder statistical algorithms. The results showed that the best-ranked references genes differed across the samples. A combination of GAPDH and EF1a would be appropriate as a reference panel for normalizing gene expression data across fruit developmental stages. A combination of EF la and SAMS would be appropriate as a reference panel for normalizing gene expression data at the stage A tested, whereas the combination of TUB a, and TEF G was the most suitable for stage B. EF2 and Hsp80 exhibited the most stable expression under stage C and stage D. NormFinder ranking of reference gene candidates was slightly different from that determined by geNorm. These results provide guidelines for the selection of reference genes under different development stages and also represent a foundation for more accurate and widespread use of qRT-PCR in L. barbarum gene analysis. (c) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:304 / 310
页数:7
相关论文
共 50 条
  • [1] Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets
    Andersen, CL
    Jensen, JL
    Orntoft, TF
    [J]. CANCER RESEARCH, 2004, 64 (15) : 5245 - 5250
  • [2] Identification and evaluation of new reference genes in Gossypium hirsutum for accurate normalization of real-time quantitative RT-PCR data
    Artico, Sinara
    Nardeli, Sarah M.
    Neto, Osmundo B. Oliveira
    Grossi-de-Sa, Maria Fatima
    Alves-Ferreira, Marcio
    [J]. BMC PLANT BIOLOGY, 2010, 10
  • [3] GAPDH as a housekeeping gene: analysis of GAPDH mRNA expression in a panel of 72 human tissues
    Barber, RD
    Harmer, DW
    Coleman, RA
    Clark, BJ
    [J]. PHYSIOLOGICAL GENOMICS, 2005, 21 (03) : 389 - 395
  • [4] Identification of suitable internal control genes for expression studies in Coffea arabica under different experimental conditions
    Barsalobres-Cavallari, Carla F.
    Severino, Fabio E.
    Maluf, Mirian P.
    Maia, Ivan G.
    [J]. BMC MOLECULAR BIOLOGY, 2009, 10
  • [5] Validating internal controls for quantitative plant gene expression studies
    Brunner A.M.
    Yakovlev I.A.
    Strauss S.H.
    [J]. BMC Plant Biology, 4 (1)
  • [6] β-Actin specifically controls cell growth, migration, and the G-actin pool
    Bunnell, Tina M.
    Burbach, Brandon J.
    Shimizu, Yoji
    Ervasti, James M.
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2011, 22 (21) : 4047 - 4058
  • [7] Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems
    Bustin, SA
    [J]. JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2002, 29 (01) : 23 - 39
  • [8] Expression profiling of the whole Arabidopsis Shaggy-like kinase multigene family by real-time reverse transcriptase-polymerase chain reaction
    Charrier, B
    Champion, A
    Henry, Y
    Kreis, M
    [J]. PLANT PHYSIOLOGY, 2002, 130 (02) : 577 - 590
  • [9] Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis
    Czechowski, T
    Stitt, M
    Altmann, T
    Udvardi, MK
    Scheible, WR
    [J]. PLANT PHYSIOLOGY, 2005, 139 (01) : 5 - 17
  • [10] Selection of internal control genes for quantitative real-time RT-PCR studies during tomato development process
    Exposito-Rodriguez, Marino
    Borges, Andres A.
    Borges-Perez, Andres
    Perez, Jose A.
    [J]. BMC PLANT BIOLOGY, 2008, 8 (1)