Identification of suitable reference genes for quantitative gene expression analysis in clam Cyclina sinensis under salinity stress and Vibrio infection
Identification of suitable reference genes for quantitative gene expression analysis in clam Cyclina sinensis under salinity stress and Vibrio infection作者机构:College of Marine and Biological EngineeringYancheng Institute of TechnologyYancheng 224051China
出 版 物:《Journal of Oceanology and Limnology》 (海洋湖沼学报(英文))
年 卷 期:2023年第41卷第1期
页 面:352-363页
核心收录:
学科分类:0710[理学-生物学] 0707[理学-海洋科学] 0906[农学-兽医学] 09[农学]
基 金:Supported by the funding for school-level research projects of Yancheng Institute of Technology(No.xjr2019047) the National Natural Science Foundation of China(No.31902362)
主 题:Cyclina sinensis reference gene different tissues salinity stress Vibrio infection
摘 要:The appropriate reference gene is a prerequisite for accurate normalization of gene expression level,and research on suitable reference genes in clam Cyclina sinensis is *** improve the situation,we selected five commonly used housekeeping genes,including β-actin,Elongation factor 1-α(EF1-α),Glyceraldehyde-3-pho sphate dehydrogenase(GAPDH),40S ribosomal protein S18(RPS18),and Tubulin a(TUB-α),then evaluated their expression stability in different adult tissues and under different experimental treatments(salinity stress and Vibrio parahaemolyticus infection).Their expression stability was analyzed by three frequently used programs,geNorm,NormFinder,and *** analysis indicated that multiple genes should be used for normalization,and we concluded that the reference gene combination GAPDH-RPS18-β-actin,should be used for qRT-PCR analysis in different tissues of *** under normal physiological *** the clams under salinity stress and Vibrio infection,EF1-α-GAPDHRPS18 was recommended as the gene combination for qRT-PCR ***-αwas generally poorly ranked by all programs,and should not be used in future *** study should provide fundamental support for accurate quantitative gene expression analysis of this species.