Faculty of Biology-Oriented Science and Technology, Kindai University, Kinokawa, Japan.
Electron Microscope Laboratory, Keio University School of Medicine, Tokyo, Japan.
Genes Cells. 2024 Oct;29(10):820-837. doi: 10.1111/gtc.13149. Epub 2024 Aug 14.
In eukaryotes, DNA is housed within the cell nucleus. Molecules required for the formation of a nucleus have been identified using in vitro systems with frog egg extracts and in vivo imaging of somatic cells. However, little is known about the physicochemical factors and conditions required for nuclear formation in mouse oocytes. In this study, using a reconstitution approach with purified DNA, we aimed to determine factors, such as the amount and timing of DNA introduction, required for the formation of nuclei with nuclear transport activity in mouse oocytes. T4 phage DNA (~166 kbp) was microinjected into strontium-activated oocytes to evaluate the conditions appropriate for nuclear formation. Microinjection of 100-500 ng/μL of T4 DNA, but not 20 ng/μL, was sufficient for the formation of nucleus-like structures. Furthermore, microinjection of DNA during metaphase II to telophase II, but not during interphase, was sufficient. Electron and fluorescence microscopy showed that T4 DNA-induced nucleus-like structures had nuclear lamina and nuclear pore complex structures similar to those of natural nuclei, as well as nuclear import activity. These results suggest that exogenous DNA can form artificial nuclei with nuclear transport functions in mouse oocytes, regardless of the sequence or source of the DNA.
在真核生物中,DNA 位于细胞核内。使用青蛙卵提取物的体外系统和体细胞的体内成像,已经鉴定出形成核所需的分子。然而,对于在小鼠卵母细胞中形成核所需的物理化学因素和条件知之甚少。在这项研究中,我们使用纯化 DNA 的重构方法,旨在确定在小鼠卵母细胞中形成具有核转运活性的核所需的因素,如 DNA 导入的量和时间。T4 噬菌体 DNA(~166 kbp)被微注射到锶激活的卵母细胞中,以评估适合核形成的条件。微注射 100-500 ng/μL 的 T4 DNA 足以形成核样结构,但 20 ng/μL 的 T4 DNA 则不足。此外,在中期至末期微注射 DNA 足以形成核样结构,但在间期则不足。电子和荧光显微镜显示,T4 DNA 诱导的核样结构具有类似于天然核的核纤层和核孔复合体结构,以及核输入活性。这些结果表明,外源 DNA 可以在小鼠卵母细胞中形成具有核转运功能的人工核,而与 DNA 的序列或来源无关。