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植物-病原菌体系芜菁黄花叶病毒(TuYV)-油菜(甘蓝型油菜)的遗传分析及 TuYV 抗性的分子标记开发。

Genetic analyses of the host-pathogen system Turnip yellows virus (TuYV)-rapeseed (Brassica napus L.) and development of molecular markers for TuYV-resistance.

机构信息

Institute for Resistance Research and Stress Tolerance, Federal Research Centre for Cultivated Plants, Julius Kühn-Institute, Erwin-Baur-Strasse 27, Quedlinburg, Germany.

出版信息

Theor Appl Genet. 2010 Feb;120(4):735-44. doi: 10.1007/s00122-009-1194-z. Epub 2009 Nov 11.

DOI:10.1007/s00122-009-1194-z
PMID:19904523
Abstract

The aphid transmitted Turnip yellows virus (TuYV) has become a serious pathogen in many rapeseed (Brassica napus L.) growing areas. Three-years' field trials were carried out to get detailed information on the genetics of TuYV resistance derived from the resynthesised B. napus line 'R54' and to develop closely linked markers. F(1) plants and segregating doubled-haploid (DH) populations derived from crosses to susceptible cultivars were analysed using artificial inoculation with virus-bearing aphids, followed by DAS-ELISA. Assuming a threshold of E (405) = 0.1 in ELISA carried out in December, the results led to the conclusion that pre-winter inhibition of TuYV is inherited in a monogenic dominant manner. However, the virus titre in most resistant lines increased during the growing period, indicating that the resistance is incomplete and that the level of the virus titre is influenced by environmental factors. Bulked-segregant marker analysis for this resistance locus identified two closely linked SSR markers along with six closely linked and three co-segregating AFLP markers. Two AFLP markers were converted into co-dominant STS markers, facilitating efficient marker-based selection for TuYV resistance. Effective markers are particularly valuable with respect to breeding for TuYV resistance, because artificial inoculation procedures using virus-bearing aphids are extremely difficult to integrate into practical rapeseed breeding programs.

摘要

蚜虫传播的芜菁黄花叶病毒(TuYV)已成为许多油菜(甘蓝型油菜)种植区的严重病原体。我们进行了为期三年的田间试验,以详细了解源自合成油菜品系 'R54' 的 TuYV 抗性的遗传学,并开发紧密连锁的标记。使用携带病毒的蚜虫进行人工接种,然后进行 DAS-ELISA,对 F(1) 植物和来自与易感品种杂交的分离加倍单倍体(DH)群体进行了分析。假设在 12 月进行的 ELISA 中 E (405) = 0.1 的阈值,则结果表明 TuYV 的冬季前抑制以单基因显性方式遗传。然而,大多数抗性系中的病毒滴度在生长期间增加,表明抗性不完全,病毒滴度水平受环境因素影响。针对该抗性位点的分组分离标记分析确定了两个紧密连锁的 SSR 标记,以及六个紧密连锁和三个共分离的 AFLP 标记。将两个 AFLP 标记转化为共显性 STS 标记,便于 TuYV 抗性的基于标记的有效选择。有效的标记在培育 TuYV 抗性方面特别有价值,因为使用携带病毒的蚜虫进行人工接种程序极难整合到实际的油菜育种计划中。

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