中国农业科学 ›› 2021, Vol. 54 ›› Issue (18): 3932-3944.doi: 10.3864/j.issn.0578-1752.2021.18.012

• 园艺 • 上一篇    下一篇

基于SLAF-seq技术鉴定苹果砧木耐涝候选基因

宋春晖1(),陈晓菲1(),王枚阁1,郑先波1,宋尚伟1,焦健1,王苗苗1,马锋旺2,白团辉1()   

  1. 1河南农业大学园艺学院,郑州 450002
    2西北农林科技大学园艺学院,杨凌 712100
  • 收稿日期:2021-01-28 接受日期:2021-04-13 出版日期:2021-09-16 发布日期:2021-09-26
  • 联系方式: 宋春晖,E-mail: songchunhui060305@126.com。|陈晓菲,E-mail: chenxiaofei0312@163.com。
  • 基金资助:
    国家重点研发计划(2019YFD1000100);国家重点研发计划(2018YFD1000300);国家自然科学基金(31872058);河南省高等学校青年骨干教师养计划(2018GGJS029);河南省大宗水果产业技术体系(Z2014-11-03)

Identification of Candidate Genes for Waterlogging Tolerance in Apple Rootstock by Using SLAF-seq Technique

SONG ChunHui1(),CHEN XiaoFei1(),WANG MeiGe1,ZHENG XianBo1,SONG ShangWei1,JIAO Jian1,WANG MiaoMiao1,MA FengWang2,BAI TuanHui1()   

  1. 1College of Horticulture, Henan Agricultural University, Zhengzhou 450002
    2College of Horticulture, Northwest A&F University, Yangling712100
  • Received:2021-01-28 Accepted:2021-04-13 Published:2021-09-16 Online:2021-09-26

摘要:

【背景】苹果(Malus×domestica Borkh)是我国主要栽培果树树种之一,但部分苹果产区由于夏、秋季的大量集中降雨和排水不良等造成果园涝害频繁发生,导致苹果树叶片黄化、脱落,果实品质和产量下降。【目的】鉴定苹果耐涝相关基因,为苹果耐涝分子标记辅助育种和优质高产栽培提供依据。【方法】以耐涝苹果砧木G41和不耐涝苹果砧木新疆野苹果(M. sieverii (Ledeb) Roem.)及其构建的包含495个F1杂交后代为材料,从F1杂交群体中挑选出耐涝和不耐涝株系各50株,构建两个极端性状DNA混池,采用简化基因组测序(SLAF-seq)技术,开发SLAF标签和SNP标记,结合苹果基因组信息和遗传关联性分析,对苹果耐涝基因进行定位及候选基因预测,并对候选基因在耐涝差异的株系中进行淹水胁迫下的表达分析。【结果】以‘金冠’苹果为参考基因组,共开发119 072个SLAF标签,其中多态性SLAF有11 133个。通过序列分析和检测SNP位点,共获得6 237 071个SNP,其中高质量SNP有170 617个。通过ED和SNP-index方法关联分析,获得一个与耐涝性状紧密关联的候选区域,位于苹果第10号染色体1.94—3.25 Mb,关联区域大小为1.31 Mb,关联区域内包含120个基因。对该区域内基因进行功能注释,发现一个与呼吸代谢相关的基因—乙醇脱氢酶基因ADH1(MD10G1014500),在淹水处理后1、2、4和6 d,该基因在耐涝植株中的表达量显著高于不耐涝植株。【结论】将苹果耐涝基因定位于第10号染色体1.94—3.25 Mb处,筛选到可能与苹果耐涝相关的候选基因MD10G1014500,可用于苹果耐涝基因的克隆和功能解析。

关键词: 苹果, 耐涝性, SLAF, SNP, 候选基因

Abstract:

【Background】 Apple (Malus×domestica Borkh) is one of the most cultivated fruit crops in China. While apple trees frequently encounter waterlogging stress mainly due to excess rainfall and poor soil drainage, resulting in yellowing leaf, declined fruit quality and yield in summer and autumn. 【Objective】 The aim of this study was to identify waterlogging-tolerant genes of apple, so as to provide a basis for waterlogging tolerance molecular marker assisted breeding, high-quality and high-yield cultivation of apple.【Method】In this study, 50 waterlogging-tolerant plants and 50 waterlogging-sensitive plants were selected to construct two bulked DNA pools from the 495 F1 population, which were derived from a cross of the waterlogging-tolerant apple rootstock G41 and the waterlogging-tolerant M. sieverii (Ledeb) Roem. Specific-locus amplified fragment (SLAF) labels and single nucleotide polymorphism (SNP) markers were developed by SLAF-seq technique. The mapping and candidate gene prediction of waterlogging tolerance in apple were carried out by combining apple genome and genetic association analysis, and the relative expression of the candidate gene was also analyzed in different waterlogging tolerance plants under waterlogging stress.【Result】A total of 119 072 SLAF labels were obtained, of which, 11 133 were polymorphic between both parents. A total 16 237 071 SNPs were identified by sequence analysis, including 170 617 SNPs with polymorphic. By association analysis with Eudidean distance (ED) and SNP-index, a candidate locus was found to be strongly associated with waterlogging tolerance, which was a region of 1.94-3.25 Mb on apple chromosome 10. The associated region was 1.31 Mb that contained 120 genes, and functional annotation of the genes in this region revealed a gene MD10G1014500, alcohol dehydrogenase gene (ADH1) related to respiratory metabolism. The expression level of ADH1 gene in waterlogging tolerant plants was significantly higher than that in waterlogging sensitive plants at 1, 2, 4 and 6 days after waterlogging treatment. 【Conclusion】 One gene (MD10G1014500) was identified as a potential candidate gene involved waterlogging tolerance of apple, which located in a 1.94-3.25 Mb interval on chromosome 10. These findings laid the foundation for gene cloning and functional analysis for waterlogging tolerance of apple.

Key words: apple, waterlogging tolerance, SLAF, SNP, candidate gene