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Identification of novel simple sequence length polymorphisms (SSLPs) in mouse by interspersed repetitive element (IRE)-PCR.

机译:通过散布的重复元件(IRE)-PCR鉴定小鼠中新的简单序列长度多态性(SSLP)。

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摘要

Interspersed repetitive element (IRE)-PCR is a useful method for identification of novel human or mouse sequence tagged sites (STSs) from contigs of genomic clones. We describe the use of IRE-PCR with mouse B1 repetitive element primers to generate novel, PCR amplifiable, simple sequence length polymorphisms (SSLPs) from yeast artificial chromosome (YAC) clones containing regions of mouse chromosomes 13 and 14. Forty-two IRE-PCR products were cloned and sequenced from eight YACs. Of these, 29 clones contained multiple simple sequence repeat units. PCR analysis with primers derived from unique sequences flanking the simple sequence repeat units in seven clones showed all to be polymorphic between various mouse strains. This novel approach to SSLP identification represents an efficient method for saturating a genomic interval with polymorphic genetic markers that may expedite the positional cloning of genes for traits and diseases.
机译:散布的重复元件(IRE)-PCR是从基因组克隆的重叠群中识别新型人或小鼠序列标记位点(STS)的有用方法。我们描述了将IRE-PCR与小鼠B1重复元件引物结合使用,以从包含小鼠13号和14号染色体区域的酵母人工染色体(YAC)克隆中产生新颖的,PCR可扩增的,简单的序列长度多态性(SSLPs)。从八个YAC中克隆PCR产物并测序。其中29个克隆包含多个简单的序列重复单元。用衍生自七个克隆中简单序列重复单元侧翼的独特序列的引物进行的PCR分析表明,在各种小鼠品系之间,它们都是多态的。这种新颖的SSLP识别方法代表了一种有效的方法,可通过多态性遗传标记物饱和基因组区间,从而加快性状和疾病基因的位置克隆。

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