Pal Debadrita, Visconti Florencia, Sepúlveda-Ramírez Silvia P, Swartz S Zachary, Shuster Charles B
Department of Biology, New Mexico State University, Las Cruces, NM, USA.
Whitehead Institute for Biomedical Research, Cambridge, MA, USA.
Methods Mol Biol. 2022;2415:1-17. doi: 10.1007/978-1-0716-1904-9_1.
The early embryos of sea urchins and other echinoderms have served as experimental models for the study of cell division since the nineteenth century. Their rapid development, optical clarity, and ease of manipulation continue to offer advantages for studying spindle assembly and cytokinesis. In the absence of transgenic lines, alternative strategies must be employed to visualize microtubules and actin. Here, we describe methods to visualize actin and microtubule using either purified, recombinant proteins, or probes in in vitro-transcribed mRNAs.
自19世纪以来,海胆和其他棘皮动物的早期胚胎就一直作为研究细胞分裂的实验模型。它们发育迅速、光学透明且易于操作,这些特点仍然为研究纺锤体组装和胞质分裂提供了优势。在没有转基因品系的情况下,必须采用其他策略来可视化微管和肌动蛋白。在这里,我们描述了使用纯化的重组蛋白或体外转录mRNA中的探针来可视化肌动蛋白和微管的方法。