Gawin B, Niederführ A, Schumacher N, Hummerich H, Little P F, Gessler M
Physiologische Chemie I, Biozentrum der Universität Würzburg, Germany.
Genome Res. 1999 Nov;9(11):1074-86. doi: 10.1101/gr.9.11.1074.
The region p13 of the short arm of human chromosome 11 has been studied intensely during the search for genes involved in the etiology of the Wilms' tumor, aniridia, genitourinary abnormalities, mental retardation (WAGR) syndrome, and related conditions. The gene map for this region is far from being complete, however, strengthening the need for additional gene identification efforts. We describe the extension of an existing contig map with P1-derived artificial chromosomes (PACs) to cover 7.5 Mb of 11p13-14.1. The extended sequence-ready contig was established by end probe walking and fingerprinting and consists of 201 PAC clones. Utilizing bins defined by overlapping PACs, we generated a detailed gene map containing 20 genes as well as 22 anonymous ESTs which have been identified by searching the RH databases. RH maps and our established gene map show global correlation, but the limits of resolution of the current RH panels are evident at this scale. Initial expression studies on the novel genes have been performed by Northern blot analyses. To extend these expression profiles, corresponding mouse cDNA clones were identified by database search and employed for Northern blot analyses and RNA in situ hybridizations to mouse embryo sections. Genomic sequencing of clones along a minimal tiling path through the contig is currently under way and will facilitate these expression studies by in silico gene identification approaches.
在寻找与威尔姆斯瘤、无虹膜、泌尿生殖系统异常、智力迟钝(WAGR)综合征及相关病症病因有关的基因过程中,人们对人类11号染色体短臂的p13区域进行了深入研究。然而,该区域的基因图谱远未完整,这就更有必要进一步开展基因识别工作。我们描述了利用P1衍生人工染色体(PAC)扩展现有重叠群图谱,使其覆盖11p13 - 14.1区域的7.5 Mb。通过末端探针步移和指纹分析建立了扩展的序列就绪重叠群,它由201个PAC克隆组成。利用由重叠PAC定义的区间,我们生成了一个详细的基因图谱,其中包含20个基因以及通过搜索RH数据库鉴定出的22个匿名EST。RH图谱与我们建立的基因图谱显示出总体相关性,但在这个尺度上,当前RH面板的分辨率极限很明显。已通过Northern印迹分析对新基因进行了初步表达研究。为了扩展这些表达谱,通过数据库搜索鉴定出相应的小鼠cDNA克隆,并将其用于Northern印迹分析以及对小鼠胚胎切片进行RNA原位杂交。目前正在对沿着重叠群的最小拼接路径的克隆进行基因组测序,这将通过计算机基因识别方法促进这些表达研究。