Jakupciak J P, Wells R D
Institute of Biosciences and Technology, Center for Genome Research, Texas A&M University, Texas Medical Center, Houston, Texas 77030, USA.
J Biol Chem. 1999 Aug 13;274(33):23468-79. doi: 10.1074/jbc.274.33.23468.
The expansion of triplet repeat sequences (TRS) associated with hereditary neurological diseases is believed from prior studies to be due to DNA replication. This report demonstrates that the expansion of (CTG.CAG)(n) in vivo also occurs by homologous recombination as shown by biochemical and genetic studies. A two-plasmid recombination system was established in Escherichia coli with derivatives of pUC19 (harboring the ampicillin resistance gene) and pACYC184 (harboring the tetracycline resistance gene). The derivatives contained various triplet repeat inserts ((CTG.CAG), (CGG.CCG), (GAA.TTC), (GTC.GAC), and (GTG.CAC)) of different lengths, orientations, and extents of interruptions and a control non-repetitive sequence. The availability of the two drug resistance genes and of several unique restriction sites on the plasmids enabled rigorous genetic and biochemical analyses. The requirements for recombination at the TRS include repeat lengths >30, the presence of CTG.CAG on both plasmids, and recA and recBC. Sequence analyses on a number of DNA products isolated from individual colonies directly demonstrated the crossing-over and expansion of the homologous CTG.CAG regions. Furthermore, inversion products of the type [(CTG)(13)(CAG)(67)].[(CTG)(67)(CAG)(13)] were isolated as the apparent result of "illegitimate" recombination events on intrahelical pseudoknots. This work establishes the relationships between CTG.CAG sequences, multiple fold expansions, genetic recombination, formation of new recombinant DNA products, and the presence of both drug resistance genes. Thus, if these reactions occur in humans, unequal crossing-over or gene conversion may also contribute to the expansions responsible for anticipation associated with several hereditary neurological syndromes.
先前的研究认为,与遗传性神经疾病相关的三联体重复序列(TRS)的扩增是由于DNA复制所致。本报告表明,通过生化和遗传学研究显示,体内(CTG.CAG)(n)的扩增也通过同源重组发生。在大肠杆菌中建立了一个双质粒重组系统,该系统由pUC19(携带氨苄青霉素抗性基因)和pACYC184(携带四环素抗性基因)的衍生物组成。这些衍生物包含不同长度、方向和中断程度的各种三联体重复插入片段((CTG.CAG)、(CGG.CCG)、(GAA.TTC)、(GTC.GAC)和(GTG.CAC))以及一个对照非重复序列。两种耐药基因的存在以及质粒上的几个独特限制酶切位点使得能够进行严格的遗传学和生化分析。TRS处重组的要求包括重复长度>30、两个质粒上都存在CTG.CAG以及recA和recBC。对从单个菌落中分离出的许多DNA产物进行的序列分析直接证明了同源CTG.CAG区域的交叉和扩增。此外,[(CTG)(13)(CAG)(67)].[(CTG)(67)(CAG)(13)]类型的倒位产物被分离出来,这显然是螺旋内假结上“非法”重组事件的结果。这项工作确立了CTG.CAG序列、多重扩增、基因重组、新重组DNA产物的形成以及两种耐药基因的存在之间的关系。因此,如果这些反应在人类中发生,不等交换或基因转换也可能导致与几种遗传性神经综合征相关的扩增。