Validation of reference genes for RT-qPCR normalization in Iris. lactea var. chinensis leaves under different experimental conditions

文献类型: 外文期刊

第一作者: Gu, Chun-Sun

作者: Gu, Chun-Sun;Lu, Xiao-Qing;Huang, Su-Zhen;Liu, Liang-Qin;Zhu, Xu-Dong;Deng, Yan-Ming

作者机构:

关键词: Iris. lactea var. chinensis;Reference genes;RT-qPCR;Abiotic stress

期刊名称:SCIENTIA HORTICULTURAE ( 影响因子:3.463; 五年影响因子:3.672 )

ISSN:

年卷期:

页码:

收录情况: SCI

摘要: Iris. lactea var. chinensis (I. lactea var. chinensis) is highly tolerant of Cu, Pb, drought, NaCl and cold. To study the molecular. mechanism of L lactea var. chinensis under these stresses, it is necessary to select reliable reference genes for RT-qPCR study. In the present study, the expression stability of nine candidate reference genes, namely, beta-tubulin (TUBLIN6), ACTIN11, translation initiation factor 4A-1 (EIF4A1), cytosolic phosphoglycerate kinase (PGK),TIP41-like family protein (TIP41), glyceraldehyde-3-phosphate dehydrogenase (GAP), phosphatase 2A (PP2Acs), cyclophilin (CYP) and ubiquitin (UBQ), was assessed in L lactea var. chinensis plants subjected to five abiotic stresses using GeNorm and NormFinder. A combination of GAP, ACTIN11, TIP41, EIF4A1 and PGK was identified as appropriate genes for normalization under PEG stress, whereas the combination of UBQ PGK, TIP41 and PP2Acs was the most suitable under NaCl stress. PP2Acs, ACTIN11 and UBQ exhibited the most stable expression under Pb stress. For Cu-treated leaves, CYP, GAP and TIP41 were the most stably expressed, while GAP, PP2Acs and TIP41 for cold-treated leaves. Generally, the analyses found that TIP41, CYP, PGK, GAP and PP2Acs were the most stable genes under five abiotic stress conditions. These results would contribute the more accurate and widespread use of RT-qPCR in I. lactea var. chinensis gene analysis

分类号: S6

  • 相关文献

[1]Assessment of reference gene stability in Rice stripe virus and Rice black streaked dwarf virus infection rice by quantitative Real-time PCR. Fang, Peng,Sun, Feng,Lan, Ying,Du, Linlin,Zhou, Yijun,Zhou, Tong,Fang, Peng,Sun, Feng,Lan, Ying,Du, Linlin,Zhou, Yijun,Zhou, Tong,Fang, Peng,Lu, Rongfei,Shen, Wenbiao. 2015

[2]Evaluation of putative internal reference genes for gene expression normalization in Nannochloropsis sp by quantitative real-time RT-PCR. Cao, Shaona,Zhang, Xiaowen,Ye, Naihao,Fan, Xiao,Xu, Dong,Cao, Shaona,Wang, Yitao,Wang, Wenqi,Liang, Chengwei. 2012

[3]Validation of Reference Genes for RT-qPCR Studies of Gene Expression in Preharvest and Postharvest Longan Fruits under Different Experimental Conditions. Wu, Jianyang,Zhang, Hongna,Liu, Liqin,Li, Weicai,Wei, Yongzan,Shi, Shengyou. 2016

[4]Evaluation of reference genes for quantitative real-time RT-PCR analysis of gene expression in Nile tilapia (Oreochromis niloticus). Yang, Chang Geng,Tian, Juan,Liu, Wei,Wu, Fan,Jiang, Ming,Wen, Hua,Wang, Xian Li.

[5]The validity of a reference gene is highly dependent on the experimental conditions in green alga Ulva linza. Zhang, Xiaowen,Xu, Dong,Ye, Naihao,Dong, Meitao,Wang, Wenqi,Chi, Xiaoyuan,Mou, Shanli,Xu, Jianfang.

[6]Candidate Reference Genes Selection and Application for RT-qPCR Analysis in Kenaf with Cytoplasmic Male Sterility Background. Chen, Peng,Khan, Aziz,Chen, Lihong,Liao, Xiaofang,Kong, Xiangjun,Zhou, Ruiyang,Zhao, Yanhong,Liu, Dongmei. 2017

[7]Systematic selection and validation of appropriate reference genes for gene expression studies by quantitative real-time PCR in pear. Xu, Yuanyuan,Li, Hui,Li, Xiaogang,Lin, Jing,Wang, Zhonghua,Yang, Qingsong,Chang, Youhong.

[8]Overexpression of Iris. lactea var. chinensis metallothionein IIMT2a enhances cadmium tolerance in Arabidopsis thaliana. Gu, Chun-Sun,Zhao, Yan-Hai,Huang, Su-Zhen,Gu, Chun-Sun,Zhao, Yan-Hai,Huang, Su-Zhen,Liu, Liang-qin,Zhu, Xu-dong,Deng, Yan-ming. 2014

[9]The Heterologous Expression of the Iris lactea var. chinensis Type 2 Metallothionein IlMT2b Gene Enhances Copper Tolerance in Arabidopsis thaliana. Gu, Chun-Sun,Huang, Su-Zhen,Lu, Xiao-Qing,Gu, Chun-Sun,Huang, Su-Zhen,Lu, Xiao-Qing,Liu, Liang-Qin,Zhu, Xu-Dong,Deng, Yan-Ming.

[10]Reference genes for quantitative real-time PCR analysis and quantitative expression of P5CS in Agropyron mongolicum under drought stress. Tian Qing-song,Du Jian-cai,Han Bing,Wang Shu-yan,Wu Zhi-juan,Li Xiao-quan,Han Bing. 2016

[11]Selection of reliable reference genes for quantitative real-time PCR gene expression analysis in Jute (Corchorus capsularis) under stress treatments. Niu, Xiaoping,Qi, Jianmin,Zhang, Gaoyang,Xu, Jiantang,Tao, Aifen,Fang, Pingping,Zhang, Gaoyang,Su, Jianguang. 2015

[12]Selection of Suitable Reference Genes for Quantitative Real-time PCR in Sapium sebiferum. Chen, Xue,Mao, Yingji,Huang, Shengwei,Ni, Jun,Lu, Weili,Hou, Jinyan,Wang, Muting,Zhao, Weiwei,Li, Minghao,Wu, Lifang,Chen, Xue,Mao, Yingji,Huang, Shengwei,Ni, Jun,Lu, Weili,Hou, Jinyan,Wang, Muting,Zhao, Weiwei,Li, Minghao,Wu, Lifang,Chen, Xue,Mao, Yingji,Lu, Weili,Wang, Muting,Lu, Weili,Wang, Muting,Wang, Qiaojian. 2017

[13]Selection of Reference Genes for Gene Expression Studies in Porcine Whole Blood and Peripheral Blood Mononuclear Cells under Polyinosinic:Polycytidylic Acid Stimulation. Wang, Jiying,Wang, Yanping,Wang, Huaizhong,Hao, Xiaojing,Wu, Ying,Guo, Jianfeng. 2014

[14]Identification of reference genes for reverse transcription quantitative real-time PCR normalization in pepper (Capsicum annuum L.). Wan, Hongjian,Yuan, Wei,Ruan, Meiying,Ye, Qingjing,Wang, Rongqing,Li, Zhimiao,Zhou, Guozhi,Yao, Zhuping,Zhao, Jing,Liu, Shujun,Yang, Yuejian. 2011

[15]Reference gene selection for quantitative real-time PCR normalization in different cherry genotypes, developmental stages and organs. Ye, Xia,Zhang, Fangming,Tao, Yonghuan,Song, Shangwei,Fang, Jinbao.

[16]Evaluation of Appropriate Reference Genes for Reverse Transcription-Quantitative PCR Studies in Different Tissues of a Desert Poplar via Comparision of Different Algorithms. Wang, Hou-Ling,Li, Lan,Yuan, Chao,Tian, Qianqian,Su, Yanyan,Li, Hui-Guang,Zhao, Lin,Yin, Weilun,Zhao, Rui,Xia, Xinli,Wang, Hou-Ling,Yin, Weilun,Tang, Sha. 2015

[17]Evaluation of Housekeeping Genes for Quantitative Real-Time PCR Analysis of Bradysia odoriphaga (Diptera: Sciaridae). Shi, Caihua,Yang, Yuting,Yang, Fengshan,Zhu, Xun,Wang, Shaoli,Wu, Qingjun,Zhang, Youjun,Du, Erxia. 2016

[18]Identification of suitable reference genes in leaves and roots of rapeseed (Brassica napus L) under different nutrient deficiencies. Han Pei-pei,Qin Lu,Li Yin-shui,Liao Xiang-sheng,Xu Zi-xian,Hu Xiao-jia,Xie Li-hua,Yu Chang-bing,Wu Yan-feng,Liao Xing. 2017

[19]In-depth analysis of internal control genes for quantitative real-time PCR in Brassica oleracea var. botrytis. Sheng, X. G.,Zhao, Z. Q.,Yu, H. F.,Wang, J. S.,Gu, H. H.,Zheng, C. F.. 2016

[20]Evaluation and validation of reference genes for SYBR Green qRT-PCR normalization in Sesamia inferens (Lepidoptera: Noctuidae). Lu, Yanhui,Zheng, Xusong,Liang, Qi,Xu, Hongxing,Yang, Yajun,Tian, Junce,Lu, Zhongxian,He, Xiaochan. 2015

作者其他论文 更多>>