AI Article Synopsis

  • Over the last 20 years, chromosome conformation capture technologies, particularly Hi-C, have enabled detailed study of genome folding in different cell types, mapping 3D chromosome structures across entire genomes.
  • When applied to mammalian preimplantation embryos, these techniques revealed a distinct chromosome organization just after fertilization, raising questions about the influence of parental origins and transcriptional status.
  • This chapter describes the application of single-cell Hi-C (scHi-C) to mouse embryos at various preimplantation stages, optimizing the limited material available and opening new research possibilities, including the study of mutant embryos for functional analysis.

Article Abstract

Over the past two decades, the development of chromosome conformation capture technologies has allowed to intensively probe the properties of genome folding in various cell types. High-throughput versions of these C-based assays (named Hi-C) have released the mapping of 3D chromosome folding for the entire genomes. Applied to mammalian preimplantation embryos, it has revealed a unique chromosome organization after fertilization when a new individual is being formed. However, the questions of whether specific structures could arise depending on their parental origins or of their transcriptional status remain open. Our method chapter is dedicated to the technical description on how applying scHi-C to mouse embryos at different stages of preimplantation development. This approach capitalized with the limited amount of material available at these developmental stages. It also provides new research avenues, such as the study of mutant embryos for further functional studies.

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Source
http://dx.doi.org/10.1007/978-1-0716-0958-3_19DOI Listing

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