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针对组蛋白缺失的HeLa细胞核残余结构的三维研究方法。

Three-dimensional approaches to the residual structure of histone-depleted HeLa cell nuclei.

作者信息

Bouvier D, Hubert J, Seve A P, Bouteille M, Moens P B

出版信息

J Ultrastruct Res. 1984 May;87(2):112-23. doi: 10.1016/s0022-5320(84)80071-4.

Abstract

Histone-depleted nuclei were prepared by high-salt extraction of interphase HeLa cell nuclei. A large amount of the nuclear DNA remained associated with a rapidly sedimenting residual nuclear structure including cytoplasmic (intermediate filament) and nuclear (matrix and lamina) proteins. Electron microscopy allowed detection in the insoluble structure of a residual nuclear envelope, nucleolar residues, and an intranuclear network whose correspondence with components of in situ fixed nuclei is discussed. Using three-dimensional electron microscopy, it is further demonstrated that the salt-insoluble structure remaining after histone depletion in 2 M NaCl is highly ordered. This is of the utmost importance when considering the roles reportedly ascribed to this structure in nuclear functions.

摘要

通过对间期HeLa细胞核进行高盐抽提制备组蛋白缺失的细胞核。大量的核DNA仍与一种快速沉降的残余核结构相关联,该结构包括细胞质(中间丝)和细胞核(基质和核纤层)蛋白。电子显微镜检测到不溶性结构中存在残余核膜、核仁残余物以及一个核内网络,本文讨论了其与原位固定细胞核成分的对应关系。利用三维电子显微镜进一步证明,在2M NaCl中组蛋白缺失后残留的盐不溶性结构是高度有序的。考虑到据报道该结构在核功能中的作用时,这一点至关重要。

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