| Literature DB >> 35412257 |
Tokuko Haraguchi1, Hiroko Osakada2, Masaaki Iwamoto3.
Abstract
Tetrahymena is a fascinating organism for studying the nuclear pore complex because it has two structurally and functionally distinct nuclei (macronucleus and micronucleus) within a cell, and there are two compositionally distinct nuclear pore complexes (NPCs) with different functions in each nucleus. Therefore, it is possible to link the function of a specific constituent protein with the nuclear function of the macronucleus and micronucleus. Additionally, these NPCs undergo dynamic changes in their structures and compositions during nuclear differentiation. Live CLEM imaging, a method of correlative light and electron microscopy (CLEM) combined with live cell imaging, is a powerful tool for visualizing these dynamic changes of specific molecules/structures of interest at high resolution. Here, we describe Live CLEM that can be applied to the study of the dynamic behavior of NPCs in Tetrahymena cells undergoing nuclear differentiation.Entities:
Keywords: CLEM; Ciliate; Correlative light and electron microscopy; Electron microscopy; Fluorescence microscopy; Live cell imaging; Nuclear envelope; Nuclear pore complex; Tetrahymena
Mesh:
Year: 2022 PMID: 35412257 DOI: 10.1007/978-1-0716-2337-4_30
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745