首页|期刊导航|西北农林科技大学学报(自然科学版)|余甘子转录组与SSR信息分析及分子标记开发

余甘子转录组与SSR信息分析及分子标记开发OA

Analysis of Phyllanthus emblica transcriptome and SSR information and molecular marker development

中文摘要英文摘要

[目的]明确余甘子转录组SSR位点的分布特征,开发余甘子SSR分子标记技术,为余甘子的亲缘关系鉴定、遗传育种和创新利用提供理论依据.[方法]以6份表型差异较大的余甘子叶片为材料,通过高通量测序技术获得余甘子叶非参转录组数据,分析其转录组和SSR位点分布特征,设计SSR引物并进行有效性和多态性筛选,最终开发余甘子SSR分子标记技术.[结果]余甘子叶转录组测序共获得65 074条基因,平均长度为1 064 bp,71.77%的基因成功获得功能注释;所有基因中共获得18 245个SSR位点,发生频率为21.68%,含有192种重复基元,其中A/T重复基元数目最多;多态性SSR位点共2 714个,占比为14.88%,表明SSR位点可用于遗传多样性分析的潜力较大.对18 245个含有SSR位点的基因进行SSR引物设计,共设计出12 488对SSR引物,成功率为73.88%,其中7 602对引物的重复基元为单核苷酸,占比为60.87%.随机挑选154对引物进行SSR位点有效性和多态性分析,筛选出10对扩增条带清晰且多态性较好的SSR引物,这10对SSR引物重复基元分别为二核苷酸7个,三核苷酸1个和五核苷酸2个,扩增产物大小为127~270 bp,平均为220.5 bp.[结论]多态性SSR位点用于余甘子遗传多样性分析的潜力较大,筛选出10对扩增条带清晰且多态性较好的SSR引物.

[Objective]This research aims to clarify the distribution characteristics of SSR loci in the transcriptome of Phyllanthus emblica and develop the SSR molecular marker technology of P.emblica,to provide a theoretical basis for the identification of genetic relationships,genetic breeding,and the innovative utilization of P.emblica.[Method]Six leaf samples of P.emblica exhibiting significant phenotypic diffe-rences were utilized as materials.Non-parametric transcriptome data for these leaves were obtained through high-throughput sequencing technology,followed by an analysis of the transcriptome and SSR locus chara-cteristics.SSR primers were then designed and evaluated for their effectiveness and polymorphism.[Re-sult]The results indicated that a total of 65 074 genes were identified through transcriptome sequencing of P.emblica leaves,with an average length of 1 064 bp.Among them,71.77%of the genes were successfully annotated.Additionally,a total of 18 245 SSR loci were identified across all genes,showing a frequency of 21.68%,which included 192 repeat motifs,with A/T repeat motifs being the most abundant.Among all lo-ci,2 714 polymorphic SSRs were detected,accounting for 14.88%,suggesting that SSR loci had great po-tential for genetic diversity analysis.A total of 12 488 pairs of SSR primers were su-ccessfully designed for the 18 245 genes containing SSR loci,with a success rate of 73.88%.Among all the primers,7 602 pairs of primers had the repeat motif of mononucleotide,accounting for 60.87%.Subsequently,154 pairs of primers were randomly selected for validation and polymorphism analysis.Ultimately,10 pairs of SSR primers ex-hibiting clear amplified bands and good polymorphism were identified.The repeat motifs of these 10 pairs consisted of 7 dinucleotides,1 trinucleotide,and 2 pentanucleotides.The size of the amplified products ranged from 127 to 270 bp,with an average of 220.5 bp.[Conclusion]Polymorphic SSR loci hold signifi-cant potential for genetic diversity.10 pairs of SSR primers,which exhibited clear amplified bands and sub-stantial polymorphism were selected.

王建超;张小艳;谢丽雪;张立杰;李韬

福建省农业科学院 果树研究所,福建 福州 350013福建省农业科学院 果树研究所,福建 福州 350013福建省农业科学院 果树研究所,福建 福州 350013福建省农业科学院 果树研究所,福建 福州 350013福建省农业科学院 果树研究所,福建 福州 350013

农业科技

余甘子转录组SSR引物筛选分子标记

Phyllanthus emblicatranscriptomeSSRprimers screeningmolecular marker

《西北农林科技大学学报(自然科学版)》 2026 (3)

35-45,11

国家热带植物种质资源库-余甘子种质资源分库项目(NTPGRC2024-011)福建省属公益类科研院所专项(2022R1028004,2024R1027002)福建省人民政府与中国农业科学院农业高质量发展超越"5511"协同创新工程项目(XTCXGC2021019-GSS01)

10.13207/j.jnwafu.2026.03.004

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