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Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region.

机译:跨越脊髓性肌萎缩疾病基因区域的酵母人工染色体重叠群的构建。

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摘要

The childhood spinal muscular atrophies (SMAs) are the most common, serious neuromuscular disorders of childhood second to Duchenne muscular dystrophy. A single locus for these disorders has been mapped by recombination events to a region of 0.7 centimorgan (range, 0.1-2.1 centimorgans) between loci D5S435 and MAP1B on chromosome 5q11.2-13.3. By using PCR amplification to screen yeast artificial chromosome (YAC) DNA pools and the PCR-vectorette method to amplify YAC ends, a YAC contig was constructed across the disease gene region. Nine walk steps identified 32 YACs, including a minimum of seven overlapping YAC clones (average size, 460 kb) that span the SMA region. The contig is characterized by a collection of 30 YAC-end sequence tag sites together with seven genetic markers. The entire YAC contig spans a minimum of 3.2 Mb; the SMA locus is confined to roughly half of this region. Microsatellite markers generated along the YAC contig segregate with the SMA locus in all families where the flanking markers (D5S435 and MAP1B) recombine. Construction of a YAC contig across the disease gene region is an essential step in isolation of the SMA-encoding gene.
机译:儿童期脊髓性肌萎缩症(SMAs)是儿童期中最常见的严重神经肌肉疾病,仅次于杜兴肌营养不良症。通过重组事件已将这些疾病的单个基因座定位在染色体5q11.2-13.3上的基因座D5S435和MAP1B之间的0.7厘摩区域(范围为0.1-2.1厘摩)。通过使用PCR扩增筛选酵母人工染色体(YAC)DNA池,并使用PCR-vectorette方法扩增YAC末端,在整个疾病基因区域构建了一个YAC重叠群。九个步行步骤确定了32个YAC,其中包括跨越SMA区的至少七个重叠的YAC克隆(平均大小,460 kb)。重叠群的特征是具有30个YAC末端序列标签位点和7个遗传标记。整个YAC重叠群的最小跨度为3.2 Mb。 SMA轨迹仅限于该区域的一半。在所有侧翼标记(D5S435和MAP1B)重组的所有家族中,沿YAC重叠群产生的微卫星标记与SMA基因座分离。跨疾病基因区域构建YAC重叠群是分离SMA编码基因的重要步骤。

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