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出 处:《上海铁道大学学报》1999年第3期9-11,共3页
摘 要:目的自人脑胶质瘤文库克隆新的表达序列标签。方法以人脑胶质瘤文库为模板,利用生长休止特异基因的5′特异引物与载体特异引物组合进行PCR扩增,对目的片段进一步克隆、测序。结果扩增出一个328bp的片段,同源性分析发现该片段与鼠SH2-B有86%的同源性。结论SH2-B是生长激素信号转导途径中酪氨酸激酶JAK2的底物,推测得到的基因片段可能介导胶质瘤的发生、发展过程中的某些信号转导途径,需克隆其cD-NA序列并研究其基因表达产物的功能方可证实。Objective It is to find a novel expressed sequence tags (EST) from a cDNA library of human brain glioblastoma.Methods PCR was carried out by using a 5′primer of growth arrest specific gene (Gas) with a pair of λ gt11 specific primers.The gene fragment of interest was cloned and sequenced.Results A 328 bp of EST was obtained and it shared 86% homology with SH2 B.Conclusion SH2 B was identified as a substrate of tyrosine kinase JAK2 in growth hormone signaling.Whether this new EST which has high homology with SH2 B mediates an unidentified signal transduction pathway in the development of human brain glioblastoma should be determined by cloning its intact cDNA sequence and investigaing its function of gene product.
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