{"title":"野生番茄品种 PI 224710(Solanum pimpinellifolium)抗晚疫病 QTL 的鉴定和绘图","authors":"Sihui Gao, Majid R. Foolad","doi":"10.1007/s11032-024-01498-1","DOIUrl":null,"url":null,"abstract":"<p>Late blight (LB), caused by oomycete <i>Phytophthora infestans</i>, is one of the most destructive diseases of the cultivated tomato, <i>Solanum lycopersicum</i>. Since new and aggressive clonal lineages of <i>P. infestans</i>, many of which overcoming formerly effective fungicides or host resistance genes, have continued to emerge, it is crucial to identify, characterize, and utilize new sources of host resistance in tomato breeding. A recent screening of tomato germplasm identified <i>Solanum pimpinellifolium</i> accession PI 224710 with very strong resistance to several current <i>P. infestans</i> clonal lineages. The present study aimed to identify and characterize QTLs associated with LB resistance in PI 224710. Disease screening of a large F<sub>2</sub> population (<i>n</i> = 1721), derived from a cross between PI 224710 and LB-susceptible tomato breeding line Fla. 8059, followed by F<sub>3</sub> progeny testing, resulted in the identification of 43 highly-resistant and 27 highly-susceptible F<sub>2</sub> individuals. A selective genotyping approach, using 469 non-identical SNP markers, resulted in the construction of a genetic linkage map and identification of three LB-resistance QTLs on chromosomes 6, 9 and 10 of PI 224710. A comparison of the QTLs genomic locations with the tomato physical map resulted in the identification of several candidate genes, which might be underpinning the LB-resistance QTLs in PI 224710. The identified markers associated with the LB-resistance QTLs can be utilized in breeding programs to transfer resistance from PI 224710 into tomato breeding lines and hybrid cultivars via marker-assisted breeding; they also can be used to develop near-isogenic lines for fine mapping of the QTLs.</p>","PeriodicalId":18769,"journal":{"name":"Molecular Breeding","volume":"1 1","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification and mapping of late blight resistance QTLs in the wild tomato accession PI 224710 (Solanum pimpinellifolium)\",\"authors\":\"Sihui Gao, Majid R. 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Disease screening of a large F<sub>2</sub> population (<i>n</i> = 1721), derived from a cross between PI 224710 and LB-susceptible tomato breeding line Fla. 8059, followed by F<sub>3</sub> progeny testing, resulted in the identification of 43 highly-resistant and 27 highly-susceptible F<sub>2</sub> individuals. A selective genotyping approach, using 469 non-identical SNP markers, resulted in the construction of a genetic linkage map and identification of three LB-resistance QTLs on chromosomes 6, 9 and 10 of PI 224710. A comparison of the QTLs genomic locations with the tomato physical map resulted in the identification of several candidate genes, which might be underpinning the LB-resistance QTLs in PI 224710. 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引用次数: 0
摘要
由卵菌 Phytophthora infestans 引起的晚疫病(LB)是栽培番茄(Solanum lycopersicum)中破坏性最强的病害之一。由于 P. infestans 不断出现新的、具有侵袭性的克隆品系,其中许多克服了以前有效的杀真菌剂或宿主抗性基因,因此在番茄育种中鉴定、描述和利用新的宿主抗性来源至关重要。最近对番茄种质进行的一次筛选发现,Solanum pimpinellifolium(番茄)登录号 PI 224710 对当前的几个 P. infestans 克隆系具有很强的抗性。本研究旨在鉴定和描述与 PI 224710 的 LB 抗性相关的 QTLs。8059 的杂交产生的大型 F2 群体(n = 1721)进行病害筛选,然后进行 F3 后代测试,最终鉴定出 43 个高抗性和 27 个高感病的 F2 个体。使用 469 个非相同 SNP 标记的选择性基因分型方法构建了遗传连锁图谱,并在 PI 224710 的 6、9 和 10 号染色体上鉴定出三个抗 LB QTL。将 QTLs 基因组位置与番茄物理图谱进行比较后,确定了几个候选基因,这些基因可能是 PI 224710 抗 LB QTLs 的基础。与抗 LB QTLs 相关的标记可用于育种计划,通过标记辅助育种将 PI 224710 的抗性转移到番茄育种品系和杂交栽培品种中;也可用于开发近等基因品系,以绘制 QTLs 的精细图谱。
Identification and mapping of late blight resistance QTLs in the wild tomato accession PI 224710 (Solanum pimpinellifolium)
Late blight (LB), caused by oomycete Phytophthora infestans, is one of the most destructive diseases of the cultivated tomato, Solanum lycopersicum. Since new and aggressive clonal lineages of P. infestans, many of which overcoming formerly effective fungicides or host resistance genes, have continued to emerge, it is crucial to identify, characterize, and utilize new sources of host resistance in tomato breeding. A recent screening of tomato germplasm identified Solanum pimpinellifolium accession PI 224710 with very strong resistance to several current P. infestans clonal lineages. The present study aimed to identify and characterize QTLs associated with LB resistance in PI 224710. Disease screening of a large F2 population (n = 1721), derived from a cross between PI 224710 and LB-susceptible tomato breeding line Fla. 8059, followed by F3 progeny testing, resulted in the identification of 43 highly-resistant and 27 highly-susceptible F2 individuals. A selective genotyping approach, using 469 non-identical SNP markers, resulted in the construction of a genetic linkage map and identification of three LB-resistance QTLs on chromosomes 6, 9 and 10 of PI 224710. A comparison of the QTLs genomic locations with the tomato physical map resulted in the identification of several candidate genes, which might be underpinning the LB-resistance QTLs in PI 224710. The identified markers associated with the LB-resistance QTLs can be utilized in breeding programs to transfer resistance from PI 224710 into tomato breeding lines and hybrid cultivars via marker-assisted breeding; they also can be used to develop near-isogenic lines for fine mapping of the QTLs.
期刊介绍:
Molecular Breeding is an international journal publishing papers on applications of plant molecular biology, i.e., research most likely leading to practical applications. The practical applications might relate to the Developing as well as the industrialised World and have demonstrable benefits for the seed industry, farmers, processing industry, the environment and the consumer.
All papers published should contribute to the understanding and progress of modern plant breeding, encompassing the scientific disciplines of molecular biology, biochemistry, genetics, physiology, pathology, plant breeding, and ecology among others.
Molecular Breeding welcomes the following categories of papers: full papers, short communications, papers describing novel methods and review papers. All submission will be subject to peer review ensuring the highest possible scientific quality standards.
Molecular Breeding core areas:
Molecular Breeding will consider manuscripts describing contemporary methods of molecular genetics and genomic analysis, structural and functional genomics in crops, proteomics and metabolic profiling, abiotic stress and field evaluation of transgenic crops containing particular traits. Manuscripts on marker assisted breeding are also of major interest, in particular novel approaches and new results of marker assisted breeding, QTL cloning, integration of conventional and marker assisted breeding, and QTL studies in crop plants.