Reference gene selection for RT-qPCR analysis of Chrysanthemum lavandulifolium during its flowering stages

被引:39
|
作者
Fu, Jianxin [1 ]
Wang, Yi [1 ]
Huang, He [1 ]
Zhang, Chao [1 ]
Dai, Silan [1 ]
机构
[1] Beijing Forestry Univ, Coll Landscape Architecture, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Reference genes; RT-qPCR; Chrysanthemum lavandulifolium; Flowering; GeNorm; REAL-TIME PCR; GENOME-WIDE IDENTIFICATION; INTERNAL CONTROL GENES; VALID REFERENCE GENES; EXPRESSION ANALYSIS; HOUSEKEEPING GENES; NORMALIZATION; LEAF;
D O I
10.1007/s11032-012-9784-x
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Quantitative real-time RT-PCR (RT-qPCR) is a technology that can be used to analyze the abundance of gene expression. Reference genes, which are assumed to remain at constant levels in different tissues at various developmental stages and photoperiodic treatments, were selected to analyze the expression levels of flowering time genes and floral development genes. Using digital gene expression technology, nine reference genes with moderate expression in the leaves of Chrysanthemum lavandulifolium at the juvenile phase (CK1) and the squaring stage (W1) were selected as the candidate reference genes for further study. A total of 115 biological samples of C. lavandulifolium were analyzed, including different tissues under various developmental stages and leaves with varied photoperiodic treatments. The stability of the nine reference genes was slightly variable across the samples, but MTP, SKIP16 and PGK were the most stable genes overall. In addition, the relative expression level of ClFT in different tissues of plants with the competence to flower was analyzed to verify the reference genes selected in this study. These studies provide a guide for selecting reference genes for analyzing the expression pattern of flowering time genes and floral development genes in C. lavandulifolium.
引用
收藏
页码:205 / 215
页数:11
相关论文
共 50 条
  • [31] Selection and validation of reference genes for accurate RT-qPCR gene expression normalization in cacao beans during fermentation
    De Wever, Jocelyn
    De Coninck, Tibo
    Everaert, Helena
    Afoakwa, Emmanuel Ohene
    Coppieters, Frauke
    Rottiers, Hayley
    Opoku, Stephen Yaw
    Lowor, Samuel
    Dewettinck, Koen
    Vandesompele, Jo
    Lefever, Steve
    Messens, Kathy
    TREE GENETICS & GENOMES, 2021, 17 (01)
  • [32] Evaluation of candidate reference genes for RT-qPCR analysis during developmental stages in striped murrel (Channa striata)
    Kumari, Rakhi
    Srivastava, Prem P.
    Mohanta, Kedar N.
    Kumar, Rajesh
    Das, Paramananda
    Sahoo, Lakshman
    Das, Gargee
    Nandanpawar, Priyanka C.
    Debbarma, Jackson
    Krishna, Gopal
    Siddaiah, Gunnur M.
    AQUACULTURE RESEARCH, 2022, 53 (18) : 6868 - 6877
  • [33] Bacterial reference genes for gene expression studies by RT-qPCR: survey and analysis
    Rocha, Danilo J. P.
    Santos, Carolina S.
    Pacheco, Luis G. C.
    ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2015, 108 (03): : 685 - 693
  • [34] Reference gene selection for gene expression studies using RT-qPCR in virus-infected planthoppers
    Guillermo A Maroniche
    Mónica Sagadín
    Vanesa C Mongelli
    Graciela A Truol
    Mariana del Vas
    Virology Journal, 8
  • [35] Reference gene selection for gene expression studies using RT-qPCR in virus-infected planthoppers
    Maroniche, Guillermo A.
    Sagadin, Monica
    Mongelli, Vanesa C.
    Truol, Graciela A.
    del Vas, Mariana
    VIROLOGY JOURNAL, 2011, 8
  • [36] Selection and validation of reference genes by RT-qPCR under photoperiodic induction of flowering in sugarcane (Saccharum spp.)
    Paulo H. da Silva Santos
    João R. Vieira Manechini
    Michael S. Brito
    Elisson Romanel
    Renato Vicentini
    Maximiliano Scarpari
    Stephen Jackson
    Luciana R. Pinto
    Scientific Reports, 11
  • [37] Selection of reference genes for accurate RT-qPCR analysis of dehydration tolerance in Xenopus laevis
    Hawkins, Liam J.
    Luu, Bryan E.
    Storey, Kenneth B.
    GENE REPORTS, 2018, 13 : 192 - 198
  • [38] RNA-seq-based selection of reference genes for RT-qPCR analysis of pitaya
    Nong, Quandong
    Yang, Yongchao
    Zhang, Mingyong
    Zhang, Mei
    Chen, Jiantong
    Jian, Shuguang
    Lu, Hongfang
    Xia, Kuaifei
    FEBS OPEN BIO, 2019, 9 (08): : 1403 - 1412
  • [39] Selection of appropriate reference genes for RT-qPCR analysis in Propylea japonica (Coleoptera: Coccinellidae)
    Lu, Jing
    Chen, Shimin
    Guo, Mujuan
    Ye, Cuiyi
    Qiu, Baoli
    Yang, Chunxiao
    Pan, Huipeng
    PLOS ONE, 2018, 13 (11):
  • [40] Stable Reference Gene Selection for RT-qPCR Analysis in Synechococcus elongatus PCC 7942 under Abiotic Stresses
    Luo, Xiao
    Li, Jiaxing
    Chang, Tianliang
    He, Hongyan
    Zhao, Yi
    Yang, Xue
    Zhao, Yuwei
    Xu, Yao
    BIOMED RESEARCH INTERNATIONAL, 2019, 2019