Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/53806
Author(s): Pereira, AJ
Matos, I
Lince-Faria, Mariana
Maiato, H
Title: Dissecting mitosis with laser microsurgery and RNAi in Drosophila cells
Issue Date: 2009
Abstract: Progress from our present understanding of the mechanisms behind mitosis has been compromised by the fact that model systems that were ideal for molecular and genetic studies (such as yeasts, C. elegans or Drosophila) were not suitable for intracellular micromanipulation. Unfortunately, those systems that were appropriate for micromanipulation (like newt lung cells, PtK1 cells or insect spermatocytes) are not amenable for molecular studies. We believe that we can significantly broaden this scenario by developing high resolution live cell microscopy tools in a system where micromanipulation studies could be combined with modern gene-interference techniques. Here we describe a series of methodologies for the functional dissection of mitosis by the use of simultaneous live cell microscopy and state-of-the-art laser microsurgery, combined with RNA interference (RNAi) in Drosophila cell lines stably expressing fluorescent markers. This technological synergism allows the specific targeting and manipulation of several structural components of the mitotic apparatus in different genetic backgrounds, at the highest spatial and temporal resolution. Finally, we demonstrate the successful adaptation of agar overlay flattening techniques to human HeLa cells and discuss the advantages of its use for laser micromanipulation and molecular studies of mitosis in mammals.
Subject: Mitosis
Drosophila
S2 cells
HeLa Cells
Live-cell microscopy
RNAi
Agar overlay
Laser microsurgery
URI: http://hdl.handle.net/10216/53806
Catalogue Link: http://dx.doi.org/10.1007/978-1-60327-993-2_9
Source: Methods in Molecular Biology, vol. 545, p.145-164
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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