Nahmias J, Hornigold N, Fitzgibbon J, Woodward K, Pilz A, Griffin D, Henske E P, Nakamura Y, Graw S, Florian F
MRC, Human Biochemical Genetics Unit, University College, London, UK.
Eur J Hum Genet. 1995;3(2):65-77. doi: 10.1159/000472279.
The tuberous sclerosis disease gene TSC1 has been mapped to 9q34. However, its precise localisation has proved problematic because of conflicting recombination data. Therefore, we have attempted to clone the entire target area into cosmid contigs prior to gene isolation studies. We have used Alu-PCR from irradiation hybrids to produce complex probes from the target region which have identified 1,400 cosmids from a chromosome-specific library. These, along with cosmids obtained by other methods, have been assembled into contigs by a fingerprinting technique. We estimate that we have obtained most of the region in cosmid contigs. These cosmids are a resource for the isolation of expressed genes within the TSC1 interval. In addition, the cosmid contig assembly has demonstrated a number of previously unknown physical connections between genes and markers in 9q34.
结节性硬化症基因TSC1已被定位于9q34。然而,由于重组数据相互矛盾,其精确位置一直存在问题。因此,在进行基因分离研究之前,我们试图将整个目标区域克隆到黏粒重叠群中。我们利用来自辐射杂种的Alu-PCR从目标区域产生复杂探针,这些探针从一个染色体特异性文库中鉴定出了1400个黏粒。这些黏粒以及通过其他方法获得的黏粒,已通过指纹技术组装成重叠群。我们估计我们已经获得了黏粒重叠群中的大部分区域。这些黏粒是分离TSC1区间内表达基因的资源。此外,黏粒重叠群组装还揭示了9q34中基因与标记之间一些以前未知的物理连接。