Hope I A, Arnold J M, McCarroll D, Jun G, Krupa A P, Herbert R
School of Biology, The University of Leeds, UK.
Mol Gen Genet. 1998 Nov;260(2-3):300-8. doi: 10.1007/s004380050899.
Promoter trapping involved screening uncharacterized fragments of C. elegans genomic DNA for C. elegans promoter activity. By sequencing the ends of these DNA fragments and locating their genomic origin using the available genome sequence data, promoter trapping has now been shown to identify real promoters of real genes, exactly as anticipated. Developmental expression patterns have thereby been linked to gene sequence, allowing further inferences on gene function to be drawn. Some expression patterns generated by promoter trapping include subcellular details. Localization to the surface of particular cells or even particular aspects of the cell surface was found to be consistent with the genes, now associated with these patterns, encoding membrane-spanning proteins. Data on gene expression patterns are easier to generate and characterize than mutant phenotypes and may provide the best means of interpreting the large quantity of sequence data currently being generated in genome projects.
启动子捕获涉及筛选秀丽隐杆线虫基因组DNA的未表征片段以检测秀丽隐杆线虫启动子活性。通过对这些DNA片段的末端进行测序,并利用现有的基因组序列数据确定其基因组来源,现已证明启动子捕获能够如预期那样识别真实基因的真实启动子。由此,发育表达模式与基因序列建立了联系,从而可以进一步推断基因功能。启动子捕获产生的一些表达模式包括亚细胞细节。发现定位于特定细胞表面甚至细胞表面的特定区域与现在与这些模式相关联的基因编码跨膜蛋白是一致的。与突变体表型相比,基因表达模式的数据更容易生成和表征,并且可能提供解释目前基因组计划中正在生成的大量序列数据的最佳方法。