利用InDel标记筛选多胚山金柑珠心苗后代  

InDel marker-assisted selection of nucellar seedlings in polyembryonic Fortunella hindsii

作　　者：宋谢天 田啸宇 王楠[1] 周银 谢源源 谢宗周[1] 柴利军[1] 叶俊丽[1] 邓秀新[1,2] SONG Xietian;TIAN Xiaoyu;WANG Nan;ZHOU Yin;XIE Yuanyuan;XIE Zongzhou;CHAI Lijun;YE Junli;DENG Xiuxin(National Key Laboratory for Germplasm lnnovation&Utilization of Horticultural Crops,Huazhong Agricultural University,Wuhan 430070,Hubei,China;Hubei Hongshan Laboratory,Wuhan 430070,Hubei,China)

机构地区：[1]华中农业大学果蔬园艺作物种质创新与利用全国重点实验室,武汉430070 [2]湖北洪山实验室,武汉430070

出　　处：《果树学报》2023年第7期1312-1317,共6页Journal of Fruit Science

基　　金：国家现代农业(柑橘)产业技术体系(CARS-26)。

摘　　要：【目的】柑橘的遗传转化通常以实生苗上胚轴为外植体。作为基因组高度杂合的无融合生殖物种,柑橘多胚种子中常含有一定比例的、因遗传重组较亲本表现出遗传背景差异的有性后代,从实生群体中筛选无性后代进行遗传转化实验可有效保证外植体材料遗传背景的一致性及后续相关研究的科学性和可靠性。基于此,开发分子标记用于快速准确筛选柑橘短童期种质——多胚山金柑(Fortunella hindsii)子代中的珠心胚实生苗,以期为优化完善山金柑遗传转化体系提供基础。【方法】利用母本山金柑材料DB02重测序数据进行InDel标记的挖掘,筛选出可以区分有性后代和无性后代的InDel标记,通过琼脂糖凝胶电泳对DB02系山金柑的子代幼苗进行鉴定。【结果】开发出7对可以区分DB02系山金柑种子中有性和无性后代的InDel杂合位点标记(InDel1~InDel7),基于这些标记进一步研究,发现土播幼苗和试管幼苗中的珠心苗比例分别为87.5%和74.2%。【结论】利用InDel标记可以成功筛选出与DB02系山金柑遗传背景一致的无性克隆后代,进一步完善了山金柑实生苗上胚轴遗传转化体系。【Objective】Citrus is a highly heterozygous genome apomixis species,and the polyembryonic seeds frequently contain a certain proportion of sexual offspring(also called zygotic embryos)that exhibit genetic background differences compared to their parents due to genetic recombination.Screening of asexual offspring(nucellar embryos)from the polyembryonic seedlings for genetic transformation experiments could effectively ensure the consistency of the genetic background of explant materials and the scientific reliability of follow-up studies.Based on this,we have developed Insertion-Deletion(InDel)molecular markers for rapid and accurate screening of asexual clonal plants in the offspring of Fortunella hindsii,a short juvenility germplasm of citrus,in order to provide a basis for optimizing and improving the genetic transformation system of F.hindsii.【Methods】The polyembryonic wild kumquat DB02 was used as the maternal parent and the progeny plants produced from DB02 seeds were used as identification materials.The seeds were sown under two conditions,one was in substrate soil and the other was in sterile test tube.Genomic DNA was extracted from the mature leaves of kumquat DB02 and its progeny,and the DNA extraction solution of qualified quality was diluted to the working concentration(about 100 ng·μL^(-1)).The re-sequencing data of the maternal DB02 was aligned to the kumquat reference genome,the InDel variant sites were extracted and the(0/1)heterozygous type sites with a difference about 50bp were screened out.The primers were designed within 600 bp around the upstream and downstream of the InDel variant site.PCR amplification products were detected by 3%agarose gel,the markers with clear and stable hybrid bands were selected.All the InDel marker primers were used to amplify the progeny of kumquat DB02 line,and the progeny with only one band was sexual seedlings.The amplification products of the InDel marker primers of the nucellar embryos were all consistent with the maternal parent.【Results】A total o

关 键 词：山金柑 珠心胚实生苗鉴定 INDEL 分子标记 

分 类 号：S666.1[农业科学—果树学]