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NANOG/NANOGP8 定位于中心体,并与中心体成熟在时空上相关联。

NANOG/NANOGP8 Localizes at the Centrosome and is Spatiotemporally Associated with Centriole Maturation.

机构信息

Department of Experimental Biology, Faculty of Science, Masaryk University, 61137 Brno, Czech Republic.

International Clinical Research Center, St. Anne's University Hospital, 65691 Brno, Czech Republic.

出版信息

Cells. 2020 Mar 11;9(3):692. doi: 10.3390/cells9030692.

Abstract

NANOG is a transcription factor involved in the regulation of pluripotency and stemness. The functional paralog of NANOG, NANOGP8, differs from NANOG in only three amino acids and exhibits similar reprogramming activity. Given the transcriptional regulatory role played by NANOG, the nuclear localization of NANOG/NANOGP8 has primarily been considered to date. In this study, we investigated the intriguing extranuclear localization of NANOG and demonstrated that a substantial pool of NANOG/NANOGP8 is localized at the centrosome. Using double immunofluorescence, the colocalization of NANOG protein with pericentrin was identified by two independent anti-NANOG antibodies among 11 tumor and non-tumor cell lines. The validity of these observations was confirmed by transient expression of GFP-tagged NANOG, which also colocalized with pericentrin. Mass spectrometry of the anti-NANOG immunoprecipitated samples verified the antibody specificity and revealed the expression of both NANOG and NANOGP8, which was further confirmed by real-time PCR. Using cell fractionation, we show that a considerable amount of NANOG protein is present in the cytoplasm of RD and NTERA-2 cells. Importantly, cytoplasmic NANOG was unevenly distributed at the centrosome pair during the cell cycle and colocalized with the distal region of the mother centriole, and its presence was markedly associated with centriole maturation. Along with the finding that the centrosomal localization of NANOG/NANOGP8 was detected in various tumor and non-tumor cell types, these results provide the first evidence suggesting a common centrosome-specific role of NANOG.

摘要

NANOG 是一种参与多能性和干细胞特性调控的转录因子。NANOG 的功能同源物 NANOGP8 仅在三个氨基酸上与 NANOG 不同,表现出相似的重编程活性。鉴于 NANOG 发挥转录调控作用,迄今为止,主要考虑了 NANOG/NANOGP8 的核定位。在这项研究中,我们研究了 NANOG 令人感兴趣的核外定位,并证明了大量的 NANOG/NANOGP8 定位于中心体。通过双免疫荧光,在 11 种肿瘤和非肿瘤细胞系中,使用两种独立的抗 NANOG 抗体鉴定出 NANOG 蛋白与中心粒周围蛋白的共定位。这些观察结果的有效性通过 GFP 标记的 NANOG 的瞬时表达得到了证实,GFP 标记的 NANOG 也与中心粒周围蛋白共定位。抗 NANOG 免疫沉淀样本的质谱分析验证了抗体的特异性,并揭示了 NANOG 和 NANOGP8 的表达,这进一步通过实时 PCR 得到了证实。通过细胞分级分离,我们表明相当数量的 NANOG 蛋白存在于 RD 和 NTERA-2 细胞的细胞质中。重要的是,细胞质 NANOG 在细胞周期中不均匀地分布在中心体对中,并与母中心粒的远端区域共定位,其存在与中心粒成熟明显相关。随着在各种肿瘤和非肿瘤细胞类型中检测到 NANOG/NANOGP8 的中心体定位的发现,这些结果首次提供了 NANOG 具有共同的中心体特异性作用的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6608/7140602/223c4563b089/cells-09-00692-g002.jpg

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