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使用序列特异性引物对 OPD20/600 进行苹果筛选。

Screening apples for OPD20/600 using sequence-specific primers.

机构信息

Department of Horticulture, University of Illinois, 310 Madigan Bldg., 1201 W. Gregory Drive, 61801, Urbana, IL, USA.

出版信息

Theor Appl Genet. 1996 Feb;92(2):263-6. doi: 10.1007/BF00223383.

DOI:10.1007/BF00223383
PMID:24166175
Abstract

Apple scab, caused by Venturia inaequalis (Cke.) Wint., is the most serious disease of apple trees in many areas of the world. Resistance to V. inaequalis, derived from the small-fruited species Malus floribunda 821, is determined by a major dominant gene, Vf. Using random decamer primers, we identified a RAPD marker, OPD20/600, which is linked to the Vf gene. OPD20/600 was then cloned and sequenced. Sequence-specific primers based on the marker were used to further screen M. floribunda 821, 7 scab-susceptible apple cultivars, 10 scab-resistant apple cultivars, and 28 scab-resistant Coop selections. The sequence-specific primers allowed identification of polymorphisms of OPD20/600 based on the presence or absence of a single band. The advantages of sequence-specific primers over decamer primers for developing genetic markers are discussed.

摘要

苹果黑星病,由梨黑星病菌(Venturia inaequalis)引起,是世界上许多地区苹果树面临的最严重病害。从小果型种苹果绵蚜(Malus floribunda)821 中获得的对梨黑星病菌的抗性,由一个主效显性基因 Vf 决定。我们使用随机十聚体引物,鉴定出与 Vf 基因连锁的 RAPD 标记 OPD20/600。随后对 OPD20/600 进行了克隆和测序。基于该标记的序列特异性引物被进一步用于筛选小果型种苹果绵蚜 821、7 个苹果品种易感黑星病、10 个苹果品种抗黑星病以及 28 个苹果抗性 Coop 系。序列特异性引物能够根据单条带的有无鉴定 OPD20/600 的多态性。讨论了与十聚体引物相比,序列特异性引物在开发遗传标记方面的优势。

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引用本文的文献

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Plant Mol Biol. 2002 Nov;50(4-5):803-18. doi: 10.1023/a:1019912419709.

本文引用的文献

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DNA "fingerprints" applied to paternity analysis in apples (Malus x domestica).将 DNA“指纹”应用于苹果(Malus x domestica)的亲子分析。
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Development of reliable PCR-based markers linked to downy mildew resistance genes in lettuce.开发与莴苣霜霉病抗性基因连锁的可靠 PCR 标记。
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