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Manipulation of Embryonic Cleavage Geometry Using Magnetic Tweezers.
Xie, Jing; Levy, Daniel L; Minc, Nicolas; Sallé, Jérémy.
Affiliation
  • Xie J; CNRS, Institut Jacques Monod, Université Paris Cité, Paris, France.
  • Levy DL; Equipe Labellisée LIGUE Contre le Cancer, Paris, France.
  • Minc N; Department of Molecular Biology, University of Wyoming, Laramie, WY, USA.
  • Sallé J; CNRS, Institut Jacques Monod, Université Paris Cité, Paris, France.
Methods Mol Biol ; 2740: 125-140, 2024.
Article in En | MEDLINE | ID: mdl-38393473
ABSTRACT
The geometry of reductive divisions that mark the development of early embryos instructs cell fates, sizes, and positions, by mechanisms that remain unclear. In that context, new methods to mechanically manipulate these divisions are starting to emerge in different model systems. These are key to develop future innovative approaches and understand developmental mechanisms controlled by cleavage geometry. In particular, how cell cycle pace is regulated in rapidly reducing blastomeres and how fate diversity can arise from blastomere size and position within embryos are fundamental questions that remain at the heart of ongoing research. In this chapter, we provide a detailed protocol to assemble and use magnetic tweezers in the sea urchin model and generate spatially controlled asymmetric and oriented divisions during early embryonic development.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cleavage Stage, Ovum / Embryonic Development Limits: Animals Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2024 Document type: Article Affiliation country: France Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cleavage Stage, Ovum / Embryonic Development Limits: Animals Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2024 Document type: Article Affiliation country: France Country of publication: United States