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使用小型荧光探针表征细胞动力学突变体。

Characterization of Cytokinetic Mutants Using Small Fluorescent Probes.

作者信息

Smertenko Andrei, Moschou Panagiotis, Zhang Laining, Fahy Deirdre, Bozhkov Peter

机构信息

Institute of Biological Chemistry, Washington State University, 646340, Pullman, WA, 99164, USA.

Institute of Global Food Security, Queen's University Belfast, 18-30 Malone Road, Belfast, BT9 5BN, UK.

出版信息

Methods Mol Biol. 2016;1370:199-208. doi: 10.1007/978-1-4939-3142-2_15.

Abstract

Cytokinesis is a powerful paradigm for addressing fundamental questions of plant biology including molecular mechanisms of development, cell division, cell signaling, membrane trafficking, cell wall synthesis, and cytoskeletal dynamics. Genetics was instrumental in identification of proteins regulating cytokinesis. Characterization of mutant lines generated using forward or reverse genetics includes microscopic analysis for defects in cell division. Typically, failure of cytokinesis results in appearance of multinucleate cells, formation of cell wall stubs, and isotropic cell expansion in the root elongation zone. Small fluorescent probes served as a very effective tool for the detection of cytokinetic defects. Such probes stain living or formaldehyde-fixed specimens avoiding complex preparatory steps. Although resolution of the fluorescence probes is inferior to electron microscopy, the procedure is fast, easy, and does not require expensive materials or equipment. This chapter describes techniques for staining DNA with the probes DAPI and SYTO82, for staining membranes with FM4-64, and for staining cell wall with propidium iodide.

摘要

胞质分裂是解决植物生物学基本问题的一个有力范例,这些问题包括发育的分子机制、细胞分裂、细胞信号传导、膜运输、细胞壁合成以及细胞骨架动力学。遗传学在鉴定调控胞质分裂的蛋白质方面发挥了重要作用。使用正向或反向遗传学产生的突变株系的表征包括对细胞分裂缺陷的显微镜分析。通常,胞质分裂失败会导致多核细胞的出现、细胞壁残端的形成以及根伸长区细胞的各向同性扩张。小型荧光探针是检测胞质分裂缺陷的一种非常有效的工具。此类探针可对活的或经甲醛固定的标本进行染色,避免了复杂的制备步骤。尽管荧光探针的分辨率低于电子显微镜,但该方法快速、简便,且不需要昂贵的材料或设备。本章介绍了用DAPI和SYTO82探针染色DNA、用FM4-64染色膜以及用碘化丙啶染色细胞壁的技术。

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