Yowe D L, Ames B N
Barker Hall, Department of Molecular, Cell Biology, Division of Biochemistry, Molecular Biology, University of California, Berkeley, CA 94720, USA.
Gene. 1998 Mar 16;209(1-2):23-30. doi: 10.1016/s0378-1119(97)00628-8.
Three age-related mtDNA deletions were identified, and the competitive polymerase chain reaction (PCR) was used to quantitate their levels in different Fisher 344 rat tissues. Deletions that removed 4834; 13273; or 13415nt of the mitochondrial genome were shown to be associated with 16 (mtDNA4834), nine (mtDNA13273), or five (mtDNA13415) nt direct repeats, respectively. The mtDNA4834 deletion was detected in an age-related manner in all tissues screened; the mtDNA13415 deletion was detected in old heart, and in both young and old brain; and the mtDNA13273 deletion was only detected in old brain tissues. The mtDNA4834 deletion was found to be at its highest level in the liver (1.88x10-2%), followed by the brain (0.22x10-2%) and kidney (0.40x10-2%) of old animals. Much lower levels were observed in old heart (0.07x10-2%) and lung (0. 04x10-2%). This distribution of mtDNA deletions in old rat tissues is in contrast to work done in humans where age-related deletions are present at the highest levels in post-mitotic tissues with much lower levels in more mitotic tissues. An inverse relationship was observed between the level of mtDNA deletions and the size of the deleted region, since the mtDNA13415 deletion was present at about a 100-fold lower level (0.53x10-5%) than the smaller mtDNA4834 deletion in old heart tissue.
鉴定出三种与年龄相关的线粒体DNA(mtDNA)缺失,并使用竞争性聚合酶链反应(PCR)对其在不同的费希尔344大鼠组织中的水平进行定量。去除线粒体基因组4834、13273或13415个核苷酸的缺失分别显示与16个(mtDNA4834)、9个(mtDNA13273)或5个(mtDNA13415)核苷酸的直接重复序列相关。在所有筛查的组织中均以与年龄相关的方式检测到mtDNA4834缺失;在老年心脏以及幼年和老年大脑中检测到mtDNA13415缺失;而mtDNA13273缺失仅在老年脑组织中检测到。发现mtDNA4834缺失在老年动物的肝脏中水平最高(1.88×10⁻²%),其次是大脑(0.22×10⁻²%)和肾脏(0.40×10⁻²%)。在老年心脏(0.07×10⁻²%)和肺(0.04×10⁻²%)中观察到的水平要低得多。老年大鼠组织中mtDNA缺失的这种分布与在人类中所做的工作形成对比,在人类中,与年龄相关的缺失在有丝分裂后组织中水平最高,而在有丝分裂较多的组织中水平要低得多。观察到mtDNA缺失水平与缺失区域大小之间呈负相关,因为在老年心脏组织中,mtDNA13415缺失的水平(0.53×10⁻⁵%)比较小的mtDNA4834缺失低约100倍。