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基于木枣与其抗裂变异系V2比较的枣裂果相关基因鉴定

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枣裂果现象普遍严重,不同品种枣果抗裂性明显不同.V2是木枣的抗裂变异系.以果实脆熟期木枣未裂果、V2未裂果及木枣裂果为材料,通过RNA-seq技术构建枣抗裂相关转录本文库,并利用qRT-PCR技术进行表达验证.结果表明,RNA-seq共得到69.6 G的原始数据,Q30达到92.7%以上,GC含量平均值为45.1%,各样品reads与参考基因组的比对效率在79.82%~85.81%之间.在木枣未裂果及V2未裂果之间筛选出50个差异表达基因,在V2中有26个基因表达上调,24个基因表达下调.在木枣未裂果与裂果之间筛选出12个差异表达基因,在裂果中有8个基因表达上调,4个基因表达下调.GO富集分析,木枣未裂果及V2未裂果之间50个差异表达基因、木枣未裂果与裂果之间12个差异表达基因分别有38、10个获得了功能注释,生物学过程在抗裂性中发挥重要作用.KEGG富集分析表明,差异表达基因主要分布在代谢相关通路,尤其是淀粉和糖代谢、嘌呤和嘧啶代谢,个别分类在遗传信息处理通路,且都未被分类在细胞过程、环境信息处理过程等通路.qRT-PCR表达验证,PHD finger蛋白基因、纤维素合成酶D5基因、bc1复合蛋白激酶基因、类甜蛋白1b基因等差异表达显著,可进行后续基因功能验证研究.
Identification of genes related to dehiscent fruit in jujube based on comparison between Muzao and its fission-resistant variation line V2
The fruit cracking of jujube is generally a serious problem,and the crack-resistance of different varieties is obviously different.V2 is a fission-resistant variation line of Muzao.The transcriptional library related to crack resistance was constructed by RNA-seq technology with the uncracked fruit of Muzao,the uncracked fruit of V2 and the cracked fruit of Muzao in fruit brittle ripening stage as test materials.The results showed that a total of 69.6 G of original data was obtained,and Q30 reached more than 92.7%with the average GC content of 45.1%.The alignment efficiency of reads between each sample and reference genome ranged from 79.82%to 85.81%by RNA-seq.Fifty differentially expressed genes were screened between the uncracked fruit of Muzao and the uncracked fruit of V2,among which 26 genes were up-regulated and 24 genes were down-regulated in V2.Twelve differentially expressed genes were screened between uncracked and cracked fruits of Muzao,among which 8 genes were up-regulated and 4 genes were down-regulated in cracked fruit.GO analysis showed that 38 of 50 and 10 of 12 differentially expressed genes between uncracked fruit of Muzao and uncracked fruit of V2,between uncracked and cracked fruits of Muzao,respectively,were functionally annotated.The biological process played an important role in crack resistance of cultivars.KEGG enrichment analysis showed that most of differentially expressed genes were distributed in metabolism-related pathways,especially starch and sucrose metabolism,purine and pyrimidine metabolism,and a few genes were classified in genetic information processing,and none of them were classified in cell processing and environmental information processing.RT-qPCR showed that the PHD finger protein gene,cellulose synthase-like protein D5 gene,protein activity of BC1 complex kinase gene and Sweet-like protein 1b gene were significantly differentially expressed,and could be used for subsequent gene functional validation studies.

jujubedehiscent fruittranscriptomegene expression

栗现芳、李晓娟、刘锦峰、邵丹、金波、陈国梁、王建华、王延峰

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延安大学生命科学学院/陕西省红枣重点实验室,陕西延安,716000

延安合源生物科技有限公司,陕西延安,716000

裂果 转录组 基因表达

2024

中国南方果树
中国农业科学院柑桔研究所

中国南方果树

CSTPCD北大核心
影响因子:0.527
ISSN:1007-1431
年,卷(期):2024.53(6)