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急性白血病骨髓细胞线粒体DNA D环区的突变检测

[Mutation detection of mitochondrial DNA D-loop region in bone marrow cells of acute leukemia].

作者信息

Han Hui, Li Da-Qi, Chen Ping, Shao Jian-Hua, Zhao Hong-Yu, Dong Xue-Bin, Gu Lin-Ping

机构信息

Department of Graduate, Weifang Medical College, Weifang, Shandong Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Feb;21(1):29-33. doi: 10.7534/j.issn.1009-2137.2013.01.007.

Abstract

This study was aimed to detect the mutations and microsatellite instability (mtMSI) in mitochondrial DNA (mtDNA) D-loop region in bone marrow cells of acute leukemia (AL) patients, and to analyze their relationship with the pathogenesis of AL. 19 cases of newly diagnosed AL were enrolled in this study. Through extracting mtDNA, the D-loop region was amplified by polymerase chain reaction (PCR), the sequences of PCR products were detected by the pros- and cons-direct sequencing methods. The sequencing results were compared with the revised Cambridge reference sequence (rCRS) and the relevant database (MITOMAP database, GenBank database, mtDB database). The results showed that the mutation rate of mtDNA D-loop region in AL was 79% (15/19). 215 variations (35 mutations, 180 SNP) and a kind of mtMSI in the D-loop region were detected. A new type of mutation nt150 C-CT was found. Also, there was no significant difference in the number of mutations between patients with different ages and different types of AL (AML, B-ALL). It is concluded that there is high frequency of mutations in the mtDNA D-loop, and the mutations may be associated with the pathogenesis of AL.

摘要

本研究旨在检测急性白血病(AL)患者骨髓细胞线粒体DNA(mtDNA)D环区域的突变及微卫星不稳定性(mtMSI),并分析其与AL发病机制的关系。本研究纳入19例新诊断的AL患者。通过提取mtDNA,采用聚合酶链反应(PCR)扩增D环区域,用正反双向测序法检测PCR产物序列。将测序结果与修订的剑桥参考序列(rCRS)及相关数据库(MITOMAP数据库、GenBank数据库、mtDB数据库)进行比对。结果显示,AL患者mtDNA D环区域的突变率为79%(15/19)。在D环区域检测到215个变异(35个突变、180个单核苷酸多态性)及一种mtMSI。发现一种新型突变nt150 C-CT。此外,不同年龄及不同类型AL(急性髓系白血病、B淋巴细胞白血病)患者的突变数量无显著差异。结论:mtDNA D环存在高频突变,这些突变可能与AL的发病机制有关。

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