利用sv40t抗原核定位信号将质粒DNA快速靶向斑马鱼胚胎细胞核。

P Collas, P Aleström
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摘要

将SV40 T抗原核定位信号(NLSs)与质粒DNA结合后,将DNA- nls复合物注射到斑马鱼卵的细胞质中,可促进转基因表达。我们现在证明,NLS肽介导DNA从细胞质输入到胚胎细胞核,在裸DNA不输入的条件下。质粒DNA通过聚合酶链反应(PCR)在分离细胞核中定位,并通过密度测定定量。将DNA与nls结合,而不是与核进口缺陷肽结合,促进DNA- nls复合物快速靶向细胞核,并在核膜上运输。DNA-NLS复合物的进口由共注射白蛋白- nls偶联物竞争。用32p标记的DNA探针的细胞核印迹检测到NLS,但未检测到反向NLS。结果表明,nls介导的DNA转移到细胞核中可能是几种基因转移应用的有价值的工具。
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Rapid targeting of plasmid DNA to zebrafish embryo nuclei by the nuclear localization signal of SV40 T antigen.

Binding SV40 T antigen nuclear localization signals (NLSs) to plasmid DNA promotes transgene expression following injection of DNA-NLS complexes into the cytoplasm of zebrafish eggs. We now demonstrate that NLS peptides mediate import of DNA from the cytoplasm into embryo nuclei, under conditions in which naked DNA is not imported. Plasmid DNA was localized by polymerase chain reaction (PCR) in isolated nuclei, and relative amounts were quantified by densitometry. Binding DNA to NLSs, but not to nuclear-import-deficient peptides, promoted rapid targeting of DNA-NLS complexes to nuclei, and transport across the nuclear envelope. Import of DNA-NLS complexes was competed by co-injected albumin-NLS conjugates. NLS, but not reverse NLS, was detected on blots of nuclei probed with 32P-labeled DNA. The results suggest that NLS-mediated DNA transfer into nuclei may constitute a valuable tool for several gene transfer applications.

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