Shin Myung-Geun, Levin Barbara C, Kim Hyeoung-Joon, Kim Hye-Ran, Lee Il-Kwon, Cho Duck, Kee Seung Jung, Shin Jong-Hee, Suh Soon-Pal, Ryang Dong-Wook
Department of Laboratory Medicine, Chonnam National University Medical School and Chonnam National University Hwasun Hospital, Hwasun, South Korea.
Electrophoresis. 2006 Apr;27(7):1331-40. doi: 10.1002/elps.200500551.
The length heteroplasmies in the hypervariable (HV) regions of mitochondrial DNA (mtDNA) from blood cells were examined in 57 healthy Korean donors. Interestingly, all the healthy Korean subjects displayed length heteroplasmies in both the HV1 and HV2 regions. Closer examination of the HV2 length heteroplasmies indicated that most of these donors (84%) exhibited a minimal 303-315 homopolymeric C (poly-C) tract frameshift of 1 bp (mixture of one major and minor mtDNA type). Sixteen percent of the donors however had poly-C tract frameshifts of 2 bp or more. The donor group with major length variants (two or more frameshifts) had about a two-fold decrease in mtDNA copy number compared with the group exhibiting only a 1 bp frameshift. This result supports the possibility that a severe frameshift in the 303-315 poly-C tract may also cause the impairment of mtDNA replication in hematopoietic tissue.
在57名健康的韩国献血者中检测了血细胞中线粒体DNA(mtDNA)高变区(HV)的长度异质性。有趣的是,所有健康的韩国受试者在HV1和HV2区域均显示出长度异质性。对HV2长度异质性的进一步检查表明,这些献血者中的大多数(84%)表现出最小303 - 315同聚C(poly-C)序列1 bp的移码(一种主要和次要mtDNA类型的混合物)。然而,16%的献血者有2 bp或更多的poly-C序列移码。与仅表现出1 bp移码的组相比,具有主要长度变异(两个或更多移码)的献血者组的mtDNA拷贝数减少了约两倍。这一结果支持了303 - 315 poly-C序列中严重移码也可能导致造血组织中mtDNA复制受损的可能性。