舒氏猪齿鱼不同组织qPCR内参基因的筛选与验证OA
Screening and validation of reference genes for qPCR in different tissues of blackspot tuskfish(Choerodon schoenleinii)
[目的]筛选在舒氏猪齿鱼不同组织中稳定表达的内参基因.[方法]选取 18 个候选内参基因 eif2s2、ube2a、actc1、rpl7l1、eif1、eif3a、ppia、rps18、rps27a、snrpd2、taf13、tor1a、tubb4b、rps27l、dera、gapdh、actg1、hsp90ab1,通过实时荧光定量PCR(qPCR)方法对其在舒氏猪齿鱼性腺、肝脏、脾脏、肾脏、肠、心脏、脑、肌肉、皮肤和鳃组织的表达进行检测,结合 BestKeeper、NormFinder、geNorm 及 RefFinder 系统评估候选基因在不同组织中表达的稳定性.[结果]18 个候选内参基因中,除 hsp90ab1 扩增效率异常外,其余引物扩增效率为 90%~103%,决定系数(R2)均大于 0.98,具有良好的扩增特异性.CT值分析显示,各基因在不同组织中的表达存在差异,其中 eif2s2 波动最小而 rps27a 波动最大.基于 BestKeeper、NormFinder、geNorm 及 RefFinder 综合分析,不同算法筛选结果总体一致,均表明eif3a、eif2s2、tubb4b 和rps27l 稳定性较高,而actc1 和gapdh 稳定性较差.geNorm 分析显示,V4/5=0.143,表明在多组织条件下采用 4 个内参基因可满足标准化要求;在单一组织中,各组织均推荐使用 2 个内参基因.[结论]tubb4b、eif2s2、eif3a 和 rps27l在 10 个组织中表达较为稳定,推荐作为舒氏猪齿鱼不同组织中 qPCR 实验的内参基因组合;另外,在单个组织中开展目标基因表达研究时,本研究推荐使用双内参组合.本研究为舒氏猪齿鱼基因表达分析及功能研究提供了可靠工具.
Blackspot tuskfish(Choerodon schoenleinii)is an economically important coral reef fish with high aquaculture value and a unique protogynous hermaphroditic reproductive pattern.Quantitative real-time PCR(qPCR)is widely used for gene expression analysis,but its accuracy depends on the use of stable reference genes.However,suitable reference genes for C.schoenleinii have not yet been systematically evaluated.To screen for stably expressed reference genes in different tissues of C.schoenleinii,eighteen candidate reference genes(eif2s2,ube2a,actc1,rpl7l1,eif1,eif3a,ppia,rps18,rps27a,snrpd2,taf13,tor1a,tubb4b,rps27l,dera,gapdh,actg1,and hsp90ab1)were selected.Their expression levels in gonad,liver,spleen,kidney,intestine,heart,brain,muscle,skin,and gill tissues were analyzed using qPCR,and expression stability was evaluated using BestKeeper,NormFinder,geNorm,and RefFinder.Among the 18 candidate genes,all except hsp90ab1 exhibited acceptable amplification efficiencies(90%-103%)and high coefficients of determination(R2>0.98),indicating good amplification spe-cificity.CT value analysis revealed variation in expression across tissues,with eif2s2 showing the least variation and rps27a the greatest.Comprehensive analysis using the four algorithms showed generally consistent results,identifying eif3a,eif2s2,tubb4b,and rps27l as the most stable genes,while actc1 and gapdh were the least stable.geNorm analysis indicated that V4/5=0.143,suggesting that four reference genes are sufficient for normalization across multiple tissues,whereas two reference genes are adequate for single-tissue analyses.Overall,tubb4b,eif2s2,eif3a,and rps27l were stably expressed across the ten tissues and are recommended as a reference gene combination for qPCR studies in different tissues of C.schoenleinii.For studies focusing on a single tissue,a dual-reference gene strategy is recommended.This study provides reliable tools for gene expres-sion analysis and functional research in C.schoenleinii.
高佳豪;陈海茹;李晓斌;赵艳飞;张宁;廖健;董忠典
广东海洋大学水产学院,南海水产经济动物增养殖重点实验室,广东 湛江 524088||广东省农业技术推广中心,广东 广州 510000广东海洋大学水产学院,南海水产经济动物增养殖重点实验室,广东 湛江 524088广东海洋大学水产学院,南海水产经济动物增养殖重点实验室,广东 湛江 524088广东省农业技术推广中心,广东 广州 510000广东海洋大学水产学院,南海水产经济动物增养殖重点实验室,广东 湛江 524088广东海洋大学水产学院,南海水产经济动物增养殖重点实验室,广东 湛江 524088广东海洋大学水产学院,南海水产经济动物增养殖重点实验室,广东 湛江 524088||广东省水产动物病害防控与健康养殖重点实验室,广东 湛江 524088
生物科学
舒氏猪齿鱼内参基因qPCR不同组织稳定性评价
Choerodon schoenleiniireference genesqPCRdifferent tissuesstability assessment
《水产学报》 2026 (6)
20-32,13
国家重点研发计划(2024YFD2401803)2025 年度广东省现代化海洋牧场适养品种核心技术攻关项目(2025-MRB-00-001)广东海洋大学水产优青项目广东海洋大学本科生创新创业项目(CXTD2023) National Key Research and Development Program of China(2024YFD2401803)2025 Guangdong Provin-cial Project on Core Technologies for Suitable Species in Modern Marine Pastures(2025-MRB-00-001)Guangdong Ocean University Outstanding Young Scholars Program in FisheriesGuangdong Ocean University Undergraduate Innovation and Startup Project(CXTD2023)
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