Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
St Vincent's Clinical School, Faculty of Medicine, University of New South Wales, Kensington, Sydney, New South Wales, Australia.
Nat Chem. 2018 Jun;10(6):631-637. doi: 10.1038/s41557-018-0046-3. Epub 2018 Apr 23.
Human genome function is underpinned by the primary storage of genetic information in canonical B-form DNA, with a second layer of DNA structure providing regulatory control. I-motif structures are thought to form in cytosine-rich regions of the genome and to have regulatory functions; however, in vivo evidence for the existence of such structures has so far remained elusive. Here we report the generation and characterization of an antibody fragment (iMab) that recognizes i-motif structures with high selectivity and affinity, enabling the detection of i-motifs in the nuclei of human cells. We demonstrate that the in vivo formation of such structures is cell-cycle and pH dependent. Furthermore, we provide evidence that i-motif structures are formed in regulatory regions of the human genome, including promoters and telomeric regions. Our results support the notion that i-motif structures provide key regulatory roles in the genome.
人类基因组的功能是由遗传信息在规范的 B 型 DNA 中的主要储存来支撑的,而第二层 DNA 结构则提供了调控控制。人们认为,发夹结构会在基因组中胞嘧啶丰富的区域形成,并具有调控功能;然而,目前在体内证明这些结构存在的证据仍然难以捉摸。在这里,我们报告了一种抗体片段(iMab)的产生和特性,该片段具有高选择性和亲和力,可以识别 DNA 中的发夹结构,并在人类细胞的核内检测到这些结构。我们证明了这些结构在体内的形成是细胞周期和 pH 值依赖性的。此外,我们提供了证据表明,发夹结构是在人类基因组的调控区域形成的,包括启动子和端粒区域。我们的结果支持了这样一种观点,即发夹结构在基因组中提供了关键的调控作用。