[1]YOO W,KIM T,LI S,et al.Reference genes for quantitative analysis on Clonorchissinensis gene expression by real-time PCR[J].Parasitol Res,2009,104:321-328. [2]HACQUARD S,VENEANLT-FOURREY C,DELARUELLE C,et al.Validation of Melampsoralarici-populina reference genes for in planta RT-quantitative PCR expression profiling during time-course infection of poplar leaves[J].Physiol Mol Plant Pathol,2011,75:106-112. [3]张玉芳,赵丽娟,曾幼玲.基因表达研究中内参基因的选择与应用[J].植物生理学，2014,50(8)：1119-1125. [4]蔡灵,吴曼丽,范丹,等.大黄鱼Hepcidin基因转录物的相对定量分析[J].上海大学学报,2012,18(4):413-418. [5]MUKESH J,AASHIMA N,AKHILESH K.et al.Validation of housekeeping genes as internal control for studying gene expression in rice by quantitative real-time PCR[J].Biochemical and Biophysical Research Communications，2006,345:646-651. [6]BUSTINS.Quantification of mRNA using real-time reverse transcription PCR (RT-PCR):trends and problems[J].J Mol Endocrinol,2002（29）:23-39. [7]DAVOREN P,MCNEILL R,LOWERY A,et al.Identification of suitable endogenous control genes for microRNA gene expression analysis in human breast cancer[J].BMC Mol Biol,2008（9）:76. [8]牙库甫江·阿西木,关波,张富春.植物基因表达转录分析中内参基因的选择与应用[J].生物技术通报，2011(7):7-11. [9]李琳琳,李天来,余朝阁,等.钙素对SA诱导番茄幼苗抗灰霉病的调控作用[J].园艺学报,2012,39(2)：273-280. [10]YANG Y,WU Y,PIRRELLO J,et al.Silencing Sl-EBF1 and Sl-EBF2 expression causes constitutive ethylene response phenotype，accelerated plant senescence，and fruit ripening in tomato [J].Journal of Experimental Botany，2009,61(3):697-708. [11]LOVDAL T,LILLOC.Reference gene selection for quantitative real-time PCR normalization in tomato subjected to nitrogen,cold,and light stress[J].Anal Biochem,2009,387:238-242. [12]FINNEGAN E,MATZKE M.Thesmall RNA world[J].J Cell Sci,2003,116(23):4689-4693. [13]金幼芳,徐根明,李艳,等.定量PCR检测microRNA表达的数据归一化新技术[J].生物化学与生物物理进展,2011,38(5):473-481. [14]任晓平,张喜春,张楠,等.低温胁迫对番茄幼苗叶片中脯氨酸降解酶的活性及其基因表达量的影响[J].中国农业通报,2012,28(10):132-135. [15]肖东,肖阳,蔡应繁,等.番茄果实成熟相关基因SlPEL和SlAPL的表达特性[J].作物学报,2010,36(7):1135-1143. [16]李仁,吴新新,李蔚,等.番茄水通道蛋白基因SlAQP的克隆与序列分析[J].中国农业科学,2012,45(2):302-310. [17]吴正景,程智慧,孟焕文.番茄叶片胞壁转化酶cDNA克隆及反义沉默表达分析[J].西北植物学报,2012,32(2):241-245. [18]TIZIANA M,ELISA S,DONATO G，et al.Evaluation of reference genes for quantitative reverse-transcription polymerase chain reaction normalization in infected tomato plants[J].Molecular Plant Pathology,2010,11(6),805-816. [19]宋圆圆,王瑞龙,魏晓晨,等.地表球囊霉诱发番茄抗早疫病的机理[J].应用生态学报,2011,22(9):2316-2324. [20]唐平华,陈国平,潘宇,等.番茄多蛋白桥梁因子基因LeMBF1的克隆及抗病性分析[J].生命科学研究,2012,16(2):138-143. [21]傅天珍,高永生,陈集双.系统侵染的番茄植株中黄瓜花叶病毒的时序变化[J].植物病理学报,2006,36(4):359-365. [22]GIOVANNA M,PIERO C,GIAN P.et al.Real-time PCR for the quantitation of Tomato yellow leaf curl Sardinia virus in tomato plants and in Bemisiatabaci[J].Journal of Virological Methods,2008,147:282-289. [23]张建成,周文静,邓秀新.超表达草生欧文氏菌crtB基因促进转基因番茄类胡萝卜素合成的研究[J].园艺学报,2010,37(3):390-396. [24]杨荣超,蔡玉静,邓春婷,等.番茄两个盐胁迫响应基因的cDNA克隆及其表达分析[J].植物科学学报,2011,29(2):178-182. [25]蒋明,郑君利.番茄(Lycopersicum esculentum)几丁质酶基因LeCHI的克隆与序列分析[J].台州学院学报,2009,31(3):44-48. [26]MAHER C,REDOUANE E M,AURLIE B,et al.Development of a real-time PCR method for the differential detection and quantification of four solanaceae in GMO analysis：Potato(Solanum tuberosum)，tomato(Solanum lycopersicum),eggplant(Solanum melongena),and pepper(Capsicum annuum) [J].J Agric Food Chem,2008,56,1818-1828. [27]YANG L T,SUN H F,PENG A H,et al.Screening and construct-specific detection methods of transgenic Huafan No 1 tomato conventional and real-time PCR[J].Journal of the Science of Food and Agriculture,2005,85:2159-2166. [28]MASCIA T,SANTOVITO E,GALLTELLID,et al.Evaluation of reference genes for quantitative reverse-transcription polymerase chain reaction normalization in infected tomato plants[J].Molecular Plant Pathology,2010,11(6)：805-816. [29]HRUZT,WYSSM,DOCQUIERM,et al.RefGenes:identification of reliable and condition specific reference genes for RT-qPCR data normalization[J].BMC Genomics,2011（12）:156. [30]EXPOSITO-RODRIGUEZ M,BORGES-ANDRES A,BORGES-PEREZ A,et al.Selection of internal control genes for quantitative real-time RT-PCR studies during tomato development process[J].BMC Plant Biology,2008（8）:131-142. [31]胡瑞波,范成明,傅永福.植物实时荧光定量PCR内参基因的选择[J].中国农业科技导报,2009,11(6):30-36. [32]胡瑞波.大豆FT_TFL1基因克隆、表达模式及功能分析[D].北京:中国农业科学院,2009. [33]COKER J,DAVIES E.Selection of candidate housekeeping controls in tomato plants using EST data[J].Bio Techniques,2003,35:740-748. [34]CZECHOWSKI T,STITT M,ALTMANN T,et al.Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis[J].Plant Physiology,2005,139:5-17. [35]BAS J,DEKKERS,LEO W,GEORGE W,et al.Densification of reference genes for RT-qPCR expression analysis in Arabidopsis and tomato seeds[J].Plant Cell Physiol,2012,53(1):28-37. [36]COVARRUBIAS A,REYES J.Post-transcriptional gene regulation of salinity and drought responses by plant microRNAs[J].Plant Cell Environ,2010,33:481-489. [37]PELTIER H,LATHAM G.Normalization of microRNA expression levels in quantitative RT-PCR assays:Identification of suitable reference RNA targets in normal and cancerous human solid tissues[J].RNA,2008,14(5)：844-852. [38]JIN W B,WU F L,XIAO L,et al.Microarray-based analysis of tomato miRNA regulated by botrytis cinerea[J].Plant Growth Regul,2012,31:38-46.