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开发与莴苣霜霉病抗性基因连锁的可靠 PCR 标记。

Development of reliable PCR-based markers linked to downy mildew resistance genes in lettuce.

机构信息

Department of Vegetable Crops, University of California, 95616, Davis, CA, USA.

出版信息

Theor Appl Genet. 1993 Feb;85(8):985-93. doi: 10.1007/BF00215038.

Abstract

Sequence characterized amplified regions (SCARs) were derived from eight random amplified polymorphic DNA (RAPD) markers linked to disease resistance genes in lettuce. SCARs are PCR-based markers that represent single, genetically defined loci that are identified by PCR amplification of genomic DNA with pairs of specific oligonucleotide primers; they may contain high-copy, dispersed genomic sequences within the amplified region. Amplified RAPD products were cloned and sequenced. The sequence was used to design 24-mer oligonucleotide primers for each end. All pairs of SCAR primers resulted in the amplification of single major bands the same size as the RAPD fragment cloned. Polymorphism was either retained as the presence or absence of amplification of the band or appeared as length polymorphisms that converted dominant RAPD loci into codominant SCAR markers. This study provided information on the molecular basis of RAPD markers. The amplified fragment contained no obvious repeated sequences beyond the primer sequence. Five out of eight pairs of SCAR primers amplified an alternate allele from both parents of the mapping population; therefore, the original RAPD polymorphism was likely due to mismatch at the primer sites.

摘要

序列特征扩增区域(SCARs)是从与生菜抗病基因连锁的 8 个随机扩增多态性 DNA(RAPD)标记中衍生出来的。SCARs 是基于 PCR 的标记,代表单一的、遗传定义的基因座,通过用一对特定的寡核苷酸引物对基因组 DNA 进行 PCR 扩增来识别;它们可能在扩增区域内包含高拷贝、分散的基因组序列。扩增的 RAPD 产物被克隆和测序。该序列被用于为每个末端设计 24 个碱基的寡核苷酸引物。所有 24 对 SCAR 引物都能扩增出与克隆的 RAPD 片段大小相同的单一主要条带。多态性要么作为带的存在或不存在而保留,要么表现为长度多态性,将显性 RAPD 基因座转化为共显性 SCAR 标记。这项研究提供了关于 RAPD 标记的分子基础的信息。扩增片段除引物序列外没有明显的重复序列。8 对 SCAR 引物中有 5 对从作图群体的双亲中扩增出了一个等位基因;因此,原始的 RAPD 多态性可能是由于引物结合位点的错配。

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