Correlation Engine 2.0
Clear Search sequence regions


Sizes of these terms reflect their relevance to your search.

Live cell imaging has tremendously promoted our understanding of cellular and subcellular processes such as cell division. Here, we present a step-by-step protocol for a robust and easy-to-use live cell imaging approach to study male meiosis in the plant Arabidopsis thaliana as recently established. Our method relies on the concomitant analysis of two reporter genes that highlight chromosome configurations and microtubule dynamics. In combination, these reporter genes allowed the discrimination of five cellular parameters: cell shape, microtubule array, nucleus position, nucleolus position, and chromatin condensation. These parameters can adopt different states, e.g., the nucleus position can be central or lateral. Analyzing how tightly these states are associated gives rise to landmark stages that in turn allow a quantitative and qualitative dissection of meiotic progression. We envision that such an approach can also provide valuable criteria for the analysis of cell differentiation processes outside of meiosis. Copyright © The Authors; exclusive licensee Bio-protocol LLC.

Citation

Maria Ada Prusicki, Emma Mathilde Keizer, Rik Peter Van Rosmalen, Christian Fleck, Arp Schnittger. Live Cell Imaging of Male Meiosis in Arabidopsis by a Landmark-based System. Bio-protocol. 2020 May 05;10(9):e3611


PMID: 33659575

View Full Text