Berg K D, Griffin C A, Eshleman J R
Department of Pathology, Johns Hopkim School of Medicine, Baltimore, MD.
Methods Mol Med. 2001;49:59-71. doi: 10.1385/1-59259-081-0:59.
In 1993, three groups independently discovered that the lengths of microsatellites in tumors could vary from the normally constant pattern defined at birth (5-5) (see review in ref. 4). This discovery has been designated either microsatellite instability (MSI) or replication errors (RER). A recent international consensus conference convened by the National Cancer Institute defined MSI/RER as "a change in length due to either insertion or deletion of repeating units, in a microsatellite within a tumor when compared to normal tissue" (5). Microsatellites are regions of repetitive DNA in which the repeating unit is small, varying in length from 1 to 6 nucleotides, and in which the number of repeating units in a microsatellite can vary from 10-60 (6-7). Because microsatellite lengths generally vary from person to person, they have received widespread use in forensics, gene mapping, parentage testing.
1993年,三个研究小组独立发现,肿瘤中微卫星的长度可能不同于出生时定义的正常恒定模式(5-5)(见参考文献4中的综述)。这一发现被称为微卫星不稳定性(MSI)或复制错误(RER)。美国国立癌症研究所最近召开的一次国际共识会议将MSI/RER定义为“与正常组织相比,肿瘤内微卫星中由于重复单元的插入或缺失而导致的长度变化”(5)。微卫星是重复DNA区域,其中重复单元很小,长度从1到6个核苷酸不等,微卫星中的重复单元数量可以从10到60个(6-7)。由于微卫星长度通常因人而异,它们在法医学、基因图谱绘制、亲子鉴定中得到了广泛应用。