Forced expression of MSR repeat transcripts above a threshold limit breaks heterochromatin organisation

Reagan W. Ching (), Kalina M. Świst-Rosowska, Galina Erikson, Birgit Koschorz, Bettina Engist and Thomas Jenuwein ()
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Reagan W. Ching: Max Planck Institute of Immunobiology and Epigenetics (MPI-IE)
Kalina M. Świst-Rosowska: Max Planck Institute of Immunobiology and Epigenetics (MPI-IE)
Galina Erikson: Max Planck Institute of Immunobiology and Epigenetics (MPI-IE)
Birgit Koschorz: Max Planck Institute of Immunobiology and Epigenetics (MPI-IE)
Bettina Engist: Max Planck Institute of Immunobiology and Epigenetics (MPI-IE)
Thomas Jenuwein: Max Planck Institute of Immunobiology and Epigenetics (MPI-IE)

Nature Communications, 2025, vol. 16, issue 1, 1-19

Abstract: Abstract Mouse heterochromatin is characterised by transcriptionally competent major satellite repeat (MSR) sequences and it has been proposed that MSR RNA contributes to the integrity of heterochromatin. We establish an inducible dCas9-effector system in mouse embryonic fibroblasts, where we can modulate MSR transcription through the targeting of a dCas9-Repressor or a dCas9-Activator. With this system, we can define a threshold limit of >300-fold deregulation of MSR transcript levels, above which the structural organisation of heterochromatin becomes disrupted. MEF cells expressing MSR RNA above this threshold limit are not viable and the defects in heterochromatin organisation and chromosome segregation cannot be reverted. This study highlights the importance of restricting MSR RNA output to maintain heterochromatin integrity and relates MSR transcript levels to either physiological or pathological conditions. It also reveals that the structural organisation of heterochromatin is governed by the transcriptional chromatin state and associated MSR RNA of the MSR repeats.

Date: 2025
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DOI: 10.1038/s41467-025-61586-4

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