首页|'羌脆李'果实发育期qRT-PCR内参基因的筛选与验证

'羌脆李'果实发育期qRT-PCR内参基因的筛选与验证

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[目的]筛选'羌脆李'果实发育过程中qRT-PCR实验合适的内参基因。[方法]选取7个(18S、Actin、EF1-α、RPL13、RPⅡ、TUB3、EF-2)常用内参基因,对'羌脆李'果实发育过程中果皮与果肉进行表达稳定性分析,使用geNorm、NormFinder、BestKeeper和RefFinder软件筛选最稳定的内参基因,并用PALI和PAL3基因验证参考基因表达水平的稳定性。[结果]'羌脆李'果实发育过程中,TUB3表达最稳定,可用于后续对李果实发育期进行基因表达的内参基因。[结论]运用4种不同的内参基因稳定性分析软件可以筛选出'羌脆李'果实发育过程中最稳定的内参基因,该结果可为李果实发育过程内参基因的选择提供参考。
Screening and Validation of Reference Genes for Real-Time PCR during'Qiangcuili'Fruit Development
[Objective]To screen suitable internal reference genes for qRT-PCR test in the fruit develop-ment of'Qiangcuili'.[Method]Seven commonly used internal reference genes(18S,Actin,EF1-α,RPL13,RP-Ⅱ,TUB3,EF-2)were selected to analyze the expression stability of pericarp and flesh during the development of'Qiangcuili'.geNorm,NormFinder,BestKeeper and RefFinder were used to assess the most stable internal reference genes.PAL1 and PAL3 gene were further employed to validate the expression stability of reference genes.[Result]The expression of TUB3 was the most stable during the fruit development of'Qiangcuili',which could be used as an internal reference gene for gene expres-sion in the subsequent fruit development period.[Conclusion]Four different internal reference gene sta-bility analysis softwares can be used to screen out the most stable internal reference genes during the de-velopment of plum fruit,and the results can provide reference for the selection of internal reference genes during the development of plum fruit.

qRT-PCRreference geneplumfruit development

唐孝富、孟银银、杜莹、王苗、蒲靖、汪红霞、牛洁、邓群仙、张慧芬

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四川农业大学园艺学院,成都 611130

qRT-PCR 内参基因 果实发育

2024

四川农业大学学报
四川农业大学

四川农业大学学报

CSTPCD北大核心
影响因子:0.657
ISSN:1000-2650
年,卷(期):2024.42(6)