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Biophysical properties of heterochromatin in totipotent mouse embryos
Biophysical properties of heterochromatin in totipotent mouse embryos
Totipotency is an incredibly plastic and transient state during the development of an embryo, which in mouse is restricted to the zygote and 2-cell stage. Indeed, totipotent embryos, are unique in terms of their chromatin architecture, metabolism and transcriptional status. Studying this short window of development is thus very important not only to better understand how normal development at these early stages occurs, but also to obtain conceptual and methodological tools to better manipulate the potency of cells in culture. During my PhD I first studied the metabolism of totipotent cells by measuring the mitochondrial membrane potential of 2-cell embryos and comparing it to pluripotent inner cell mass and differentiated trophectoderm of blastocysts. My results show, that although these two embryo stages differ in their oxygen consumption and mitochondria matrix shape, there are no major changes in mitochondrial membrane potential. The main objective of my PhD was the characterization of the biophysical properties of heterochromatin during the process of chromocenter formation that occurs at the 2-cell stage. I first identified a set of core heterochromatic proteins and revealed their higher potential to phase separate based on an in silico analysis. Using a wide variety of microscopy techniques, I showed that pericentromeric heterochromatin transitions from a liquid state to a more solid or gel like state during the process of chromocenter formation. Overall, my work contributes to a better understanding of the features that characterise totipotency as well as developing state of the art tools to study the biophysical properties of constitutive heterochromatin at these early stages of development.
Embryology, Development, Epigenetics, Phase separation
Guthmann, Manuel
2023
English
Universitätsbibliothek der Ludwig-Maximilians-Universität München
Guthmann, Manuel (2023): Biophysical properties of heterochromatin in totipotent mouse embryos. Dissertation, LMU München: Faculty of Biology
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Abstract

Totipotency is an incredibly plastic and transient state during the development of an embryo, which in mouse is restricted to the zygote and 2-cell stage. Indeed, totipotent embryos, are unique in terms of their chromatin architecture, metabolism and transcriptional status. Studying this short window of development is thus very important not only to better understand how normal development at these early stages occurs, but also to obtain conceptual and methodological tools to better manipulate the potency of cells in culture. During my PhD I first studied the metabolism of totipotent cells by measuring the mitochondrial membrane potential of 2-cell embryos and comparing it to pluripotent inner cell mass and differentiated trophectoderm of blastocysts. My results show, that although these two embryo stages differ in their oxygen consumption and mitochondria matrix shape, there are no major changes in mitochondrial membrane potential. The main objective of my PhD was the characterization of the biophysical properties of heterochromatin during the process of chromocenter formation that occurs at the 2-cell stage. I first identified a set of core heterochromatic proteins and revealed their higher potential to phase separate based on an in silico analysis. Using a wide variety of microscopy techniques, I showed that pericentromeric heterochromatin transitions from a liquid state to a more solid or gel like state during the process of chromocenter formation. Overall, my work contributes to a better understanding of the features that characterise totipotency as well as developing state of the art tools to study the biophysical properties of constitutive heterochromatin at these early stages of development.