Noguchi Eri, Shigi Narumi, Komiyama Makoto
Research Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, Japan 153-8904.
Nat Prod Commun. 2012 Mar;7(3):349-52.
Peptide nucleic acid (PNA) is one of the most useful DNA analogs in a wide variety of gene analysis in human cells. In order to exhibit its maximal functions, PNA must be localized to a desired place (e.g., nucleus, cytoplasm and other organelles). Here, we introduced PNAs into HeLa cells by electroporation and examined their localization at various time points. The PNA which binds to the mitochondrial COII gene was initially accumulated in the nucleus, and thereafter mostly transferred to cytoplasm. This time-dependent intracellular localization of PNA is ascribed to the breakdown of the nuclear envelope in the cell division. On the other hand, another PNA that binds to telomere repeat sequence mostly remained in the nucleus, even after the cell division occurred. The retention of this PNA in the nucleus was further enhanced when it was conjugated with Cy3.
肽核酸(PNA)是人类细胞各种基因分析中最有用的DNA类似物之一。为了发挥其最大功能,PNA必须定位于所需位置(如细胞核、细胞质和其他细胞器)。在这里,我们通过电穿孔将PNA导入HeLa细胞,并在不同时间点检查它们的定位。与线粒体COII基因结合的PNA最初积聚在细胞核中,然后大部分转移到细胞质中。PNA这种随时间变化的细胞内定位归因于细胞分裂时核膜的破裂。另一方面,另一种与端粒重复序列结合的PNA即使在细胞分裂发生后也大多保留在细胞核中。当它与Cy3偶联时,这种PNA在细胞核中的保留进一步增强。