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作 者:仲悦娇[1] 陈宝安[1] 程璐[2] 冯继峰 李玉峰[4] 钱军[5] 丁家华[1] 程坚[1] 高峰[1] 夏国华[1] 孙宁[1] 张琰[1] 张孝平[1] 许佩佩[1] 陆祖宏[2]
机构地区:[1]东南大学临床医学院附属中大医院血液科,江苏南京210009 [2]东南大学生物科学与医学工程学院生物电子学国家重点实验室,江苏南京210096 [3]江苏省肿瘤研究所,江苏南京210009 [4]淮安市第一人民医院,江苏淮安223300 [5]镇江市第一人民医院,江苏镇江212002
出 处:《中国实验血液学杂志》2009年第5期1234-1237,共4页Journal of Experimental Hematology
基 金:国家自然基金资助面上项目(编号30872970);江苏省自然基金项目(编号BK2005203)
摘 要:本研究探讨基质辅助激光解吸电离飞行时间质谱技术(MALDI-TOFMS)检测多发性骨髓瘤(MM)jak2基因的单核苷酸多态性(SNP)的实用性。用PCR扩增出含jak2基因2个SNP(C428T和C643T)位点的DNA片段作为模板,产物纯化后利用MALDI-TOFMS检测5例MM和5例健康对照者样本的jak2基因多态性。结果表明:C428T和C643T位点基因型在多发性骨髓瘤病例与健康对照组的分布无差异,均为T/T纯合子。结论:本实验建立的基于MALDI-TOFMS与引物延伸技术检测jak2基因多态性的方法是一个快速、准确和可靠的检测方法。This study was purposed to investigate the practicality of matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS ) for detection of single nucleotide polymorphisms(SNP) on jak2 gene in multiple myeloma (MM) cells. The DNA fragment containing 2 SNPs of jak2 (C428T and C643T) was amplified using PCR and was purified. The purified product was used as the template for primer extension (PEX). The small products of allele-specific reaction were purified, the SNPs on jak2 gene of 5 patients with MM and 5 healthy persons were detected by MALDI-TOF MS. The results showed that the distribution of genotype C428T and C643T was not different between MM patients and healthy persons, both of which are hamozygous T/T. In conclusion, the method based on MALDI-TOF MS and PEX technique for detecting SNP in jak2 gene is rapid, accurate and reliable method, and can be used in clinical practise.
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