Van Tuyle G C, Gudikote J P, Hurt V R, Miller B B, Moore C A
Department of Biochemistry and Molecular Biophysics, Virginia Commonwealth University, Richmond 23298, USA.
Mutat Res. 1996 Jan 17;349(1):95-107. doi: 10.1016/0027-5107(95)00165-4.
This study identified 33 different deletions in mitochondrial DNA from four aging Fischer-344 rat brains and from a cultured rat lymphoma cell line (Nb2 cells). The deletions were located in the longer arc between the heavy and light strand origins of replication. PCR products that spanned across the deleted regions were sequenced, and deletions ranging between 6548 bp and 9977 bp in length were identified. Short direct repeats of < or = 8 bp were present at the end points of all but one of the deletions. The remaining deletion contained, instead, a near-perfect direct repeat (9/10 bp) within two base pairs of its end points. In 24 of the deletions, a sequence equivalent to one member of the paired direct repeats was lost with the deleted segment. In the remaining nine, either more or less of the base pairs of a single repeat were lost. Twelve of the 33 different deletions terminated on one side at a common locus (major hot spot) of 5 bp in length, located at the 5' end of the tRNAThr gene. The opposite ends of these 12 deletions were at different sites. The hot spot was located in a region of the mtDNA with strong potential for secondary structure and was flanked by a pair of AT-rich sequences. The utilization of the hot spot as an end point for deletions appeared to be widespread in that it was represented in 1/3-1/2 of the deletions characterized in each of the five mtDNA sources examined. In addition, several minor hot spots, where one end of two or three different deletions coincided, were also identified.
本研究在来自四只衰老的Fischer-344大鼠大脑以及一个培养的大鼠淋巴瘤细胞系(Nb2细胞)的线粒体DNA中鉴定出33种不同的缺失。这些缺失位于重链和轻链复制起点之间的较长弧段上。对跨越缺失区域的PCR产物进行了测序,鉴定出长度在6548 bp至9977 bp之间的缺失。除一个缺失外,所有缺失的端点均存在长度≤8 bp的短直接重复序列。其余的缺失在其端点的两个碱基对范围内包含一个近乎完美的直接重复序列(9/10 bp)。在24个缺失中,与配对直接重复序列之一相同的序列随缺失片段一起丢失。在其余9个缺失中,单个重复序列的碱基对或多或少有所丢失。33种不同缺失中的12种在一侧终止于一个长度为5 bp的共同位点(主要热点),该位点位于tRNAThr基因的5'端。这12个缺失的另一端位于不同位点。该热点位于mtDNA中具有强烈二级结构潜力的区域,两侧是一对富含AT的序列。该热点作为缺失端点的利用似乎很普遍,因为在所检查的五个mtDNA来源中的每一个中,其在1/3 - 1/2的已鉴定缺失中都有出现。此外,还鉴定出了几个次要热点,其中两到三个不同缺失的一端重合。