[1]朱雪梅,郭广君,潘宝贵,等.辣椒抗PMMoV基因L4连锁标记的验证分析[J].江苏农业学报,2022,38(06):1627-1636.[doi:doi:10.3969/j.issn.1000-4440.2022.06.022]
 ZHU Xue-mei,GUO Guang-jun,PAN Bao-gui,et al.Test analysis of L4-linked markers for PMMoV resistant gene in pepper[J].,2022,38(06):1627-1636.[doi:doi:10.3969/j.issn.1000-4440.2022.06.022]
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辣椒抗PMMoV基因L4连锁标记的验证分析()
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江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
38
期数:
2022年06期
页码:
1627-1636
栏目:
园艺
出版日期:
2022-12-31

文章信息/Info

Title:
Test analysis of L4-linked markers for PMMoV resistant gene in pepper
作者:
朱雪梅12郭广君2潘宝贵2刁卫平2刘金兵2高长洲2王述彬2
(1.南京农业大学园艺学院,江苏南京210095;2.江苏省农业科学院蔬菜研究所/江苏省高效园艺作物遗传改良重点实验室,江苏南京210014)
Author(s):
ZHU Xue-mei12GUO Guang-jun2PAN Bao-gui2DIAO Wei-ping2LIU Jin-bing2GAO Chang-zhou2WANG Shu-bin2
(1.College of Horticulture, Nanjing Agricultural University, Nanjing 210095, China;2.Institute of Vegetable Crops, Jiangsu Academy of Agricultural Sciences/Jiangsu Key Laboratory for Efficient Horticultural Crop Genetic Improvement,Nanjing 210014,China)
关键词:
辣椒辣椒轻斑驳病毒分子标记辅助筛选
Keywords:
pepperpepper mild mottle virusmolecular marker assisted selection
分类号:
S641.3
DOI:
doi:10.3969/j.issn.1000-4440.2022.06.022
文献标志码:
A
摘要:
近年来,辣椒轻斑驳病毒(Pepper mild mottle virus,PMMoV)病的发生日趋严重,已严重危害中国辣椒生产。L系列等位基因(L1、L2、L3、L4)是抗烟草花叶病毒属的主要抗性基因,其中L4基因抗性最强且具有广谱性。为加速L4基因的转育应用,本研究对前人报道的3对与L4基因紧密连锁的分子标记进行检验分析。结果显示,标记L4SC340退火温度不稳定,极易造成假阳性,不适用于L4抗性基因的辅助筛选。标记087H3T7和L4-SCAR可以筛选出携带L3和L4抗性基因的辣椒种质,但无法区分携带L3和L4基因的抗性材料,同时087H3T7存在杂合基因型过高的问题。二者比较来说,L4-SCAR标记的筛选准确度高于087H3T7,但是L4-SCAR为显性标记,无法区分杂合基因型。因此上述3对标记均不能用于筛选携带L4抗性基因的种质材料,但是在明确抗性材料基因型的情况下,L4-SCAR标记结合087H3T7可用于L3和L4抗性基因转育后代抗性单株的辅助筛选。本研究结果可为加速辣椒抗PMMoV育种提供更实用的分子标记。
Abstract:
In recent years, disease caused by pepper mild mottle virus (PMMoV) has become more and more serious and has harmed pepper production in China severely. L-series allelic genes (L1, L2, L3, L4) are the main resistant genes against tobamovirus, and L4 gene was reported to show the strongest resistant to tobamovirus with a broad spectrum. In order to accelerate the application of transgenic breeding of the L4 gene, three pairs of reported molecular markers closely linked to L4 gene were examined and analyzed in this study. The results showed that, the annealing temperature of marker L4SC340 was unstable and could easily cause false positives, so L4SC340 was unsuitable for the assisted screening of L4 resistant gene. Markers 087H3T7 and L4-SCAR could be used to screen pepper germplasms carrying L3 and L4 resistant genes, but they could not be used to distinguish resistant materials carrying L3 and L4 genes. Meanwhile, 087H3T7 had the problem of excessive heterozygous genotypes. In comparison, the screening accuracy of L4-SCAR marker was higher than that of 087H3T7, but L4-SCAR was a dominant marker that could not distinguish heterozygous genotype. Therefore, none of the three pairs of markers could be used to screen the germplasm material carrying L4 resistant gene. However, through clarifying the genotype of the resistant materials, L4-SCAR marker combined with 087H3T7 could be used for assisted screening of resistant individuals in the breeding of transgenic progeny with L3 and L4 resistant genes. Results of the study can provide more practical molecular markers for accelerated breeding of PMMoV resistant pepper.

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备注/Memo

备注/Memo:
收稿日期:2022-04-07基金项目:国家自然科学基金面上项目(32072597);江苏省种业振兴揭榜挂帅项目[JBGS(2021)065];国家现代农业产业技术体系建设专项(CARS-23-G42)作者简介:朱雪梅 (1996-),女,山东滨州人,硕士研究生,主要研究方向为辣椒遗传育种和分子生物学。(E-mail)1668178637@qq.com。郭广君为共同第一作者。通讯作者:王述彬,(E-mail)wangsbpep@163.com
更新日期/Last Update: 2023-01-13