D'Ugo E, Bruni R, Argentini C, Giuseppetti R, Rapicetta M
Laboratory of Virology, Istituto Superiore di Sanità, Rome, Italy.
DNA Cell Biol. 1998 Jun;17(6):519-27. doi: 10.1089/dna.1998.17.519.
Scaffold or matrix attachment regions (S/MARs) are noncoding genomic DNA sequences displaying in vitro selective binding affinity for nuclear scaffold. They have been reported to be involved in the physical attachment of genomic DNA to the nuclear scaffold, and thus in the organization of the chromatin in functional loops or domains, and in the regulation of gene expression. In this work, we report the identification of an S/MAR in a woodchuck chromosomal locus, named b3n, previously described as a recurrent site of woodchuck hepatitis virus (WHV) DNA integration in woodchuck hepatocellular carcinoma (HCC). The 4.3-kb sequence of this locus contains several Alu-like repeats and a gag-like coding region with frameshift mutations. Computer analysis revealed the presence of a region with unusually high AT content, typical of most S/MARs, and of specific motifs (A boxes, T boxes, topoisomerase II sites, and unwinding elements) overlapping or in proximity to the region with high AT content, predicting that b3n might contain an S/MAR. Fragments of the b3n locus were isolated by conventional and inverse PCR techniques. In in vitro binding experiments with both heterologous and autologous scaffold preparations, a 592-bp fragment spanning the region rich in S/MAR features showed marked scaffold affinity, which was specific when autologous scaffolds were used. The presence of an S/MAR at the b3n locus and its nature as a recurrent WHV integration site in HCC suggest the involvement of S/MAR elements in some of the mechanisms leading to liver oncogenesis.
支架或基质附着区域(S/MARs)是一类非编码基因组DNA序列,在体外对核支架具有选择性结合亲和力。据报道,它们参与基因组DNA与核支架的物理附着,进而参与染色质在功能环或结构域中的组织以及基因表达的调控。在本研究中,我们报告了在土拨鼠染色体位点b3n中鉴定出一个S/MAR,该位点先前被描述为土拨鼠肝炎病毒(WHV)DNA在土拨鼠肝细胞癌(HCC)中反复整合的位点。该位点的4.3 kb序列包含几个类似Alu的重复序列和一个带有移码突变的类似gag的编码区域。计算机分析显示存在一个AT含量异常高的区域,这是大多数S/MARs的典型特征,并且存在与高AT含量区域重叠或相邻的特定基序(A框、T框、拓扑异构酶II位点和解旋元件),预测b3n可能包含一个S/MAR。通过常规PCR和反向PCR技术分离出b3n位点的片段。在与异源和同源支架制剂的体外结合实验中,一个跨越富含S/MAR特征区域的592 bp片段显示出明显的支架亲和力,当使用同源支架时这种亲和力具有特异性。b3n位点存在S/MAR及其作为HCC中WHV反复整合位点的性质表明S/MAR元件参与了导致肝癌发生的一些机制。