Li Ling-Hui, Li Jian-Chiuan, Lin Yung-Feng, Lin Chung-Yen, Chen Chung-Yung, Tsai Shih-Feng
Division of Molecular and Genomic Medicine, National Health Research Institutes, Taipei, Taiwan.
Nucleic Acids Res. 2004 Feb 11;32(3):e27. doi: 10.1093/nar/gnh025.
To facilitate transcript mapping and to investigate alterations in genomic structure and gene expression in a defined genomic target, we developed a novel microarray-based method to detect transcriptional activity of the human chromosome 4q22-24 region. Loss of heterozygosity of human 4q22-24 is frequently observed in hepatocellular carcinoma (HCC). One hundred and eighteen well-characterized genes have been identified from this region. We took previously sequenced shotgun subclones as templates to amplify overlapping sequences for the genomic segment and constructed a chromosome-region-specific microarray. Using genomic DNA fragments as probes, we detected transcriptional activity from within this region among five different tissues. The hybridization results indicate that there are new transcripts that have not yet been identified by other methods. The existence of new transcripts encoded by genes in this region was confirmed by PCR cloning or cDNA library screening. The procedure reported here allows coupling of shotgun sequencing with transcript mapping and, potentially, detailed analysis of gene expression and chromosomal copy of the genomic sequence for the putative HCC tumor suppressor gene(s) in the 4q candidate region.
为便于转录本定位,并研究特定基因组靶点的基因组结构改变和基因表达,我们开发了一种基于微阵列的新方法,用于检测人类染色体4q22 - 24区域的转录活性。在肝细胞癌(HCC)中经常观察到人类4q22 - 24的杂合性缺失。已从该区域鉴定出118个特征明确的基因。我们以前测的鸟枪法亚克隆为模板,扩增基因组片段的重叠序列,并构建了染色体区域特异性微阵列。使用基因组DNA片段作为探针,我们检测了五个不同组织中该区域内的转录活性。杂交结果表明存在尚未被其他方法鉴定的新转录本。通过PCR克隆或cDNA文库筛选证实了该区域基因编码的新转录本的存在。本文报道的方法允许将鸟枪法测序与转录本定位相结合,并有可能对4q候选区域中假定的HCC肿瘤抑制基因的基因表达和基因组序列的染色体拷贝进行详细分析。