Abstract

Most autosomal genes are thought to be expressed from both alleles, with some notable exceptions, including imprinted genes and genes showing random monoallelic expression (RME). The extent and nature of RME has been the subject of debate. Here we investigate the expression of several candidate RME genes in F1 hybrid mouse cells before and after differentiation, to define how they become persistently, monoallelically expressed. Clonal monoallelic expression is not present in embryonic stem cells, but we observe high frequencies of monoallelism in neuronal progenitor cells by assessing expression status in more than 200 clones. We uncover unforeseen modes of allelic expression that appear to be gene-specific and epigenetically regulated. This non-canonical allelic regulation has important implications for development and disease, including autosomal dominant disorders and opens up therapeutic perspectives.

Some autosomal genes are expressed in a random monoallelic manner, but its extent and mechanisms have remained unclear. Here the authors show robust monoallelic expression in cell lines and mice, where the silent allele can be reexpressed using epidrugs. Further, they find these genes display various modalities of allelic expression with different degrees of allelic imbalance.

Details

Title
Locus specific epigenetic modalities of random allelic expression imbalance
Author
Marion-Poll Lucile 1   VIAFID ORCID Logo  ; Forêt Benjamin 2 ; Zielinski, Dina 3   VIAFID ORCID Logo  ; Massip Florian 4 ; Attia Mikael 5 ; Carter, Ava C 6 ; Laurène, Syx 7 ; Chang, Howard Y 6   VIAFID ORCID Logo  ; Anne-Valerie, Gendrel 8   VIAFID ORCID Logo  ; Heard, Edith 9 

 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France; Directors’ research, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany (GRID:grid.4709.a) (ISNI:0000 0004 0495 846X) 
 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France (GRID:grid.4709.a) 
 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France (GRID:grid.4709.a); Institut Curie, PSL Research University, INSERM U900, Mines ParisTech, Paris, France (GRID:grid.4709.a) 
 Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine, Berlin, Germany (GRID:grid.419491.0) (ISNI:0000 0001 1014 0849) 
 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France (GRID:grid.419491.0) 
 Stanford University, Center for Personal Dynamic Regulomes, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France (GRID:grid.168010.e); Institut Curie, PSL Research University, INSERM U900, Mines ParisTech, Paris, France (GRID:grid.168010.e) 
 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France (GRID:grid.168010.e) 
 Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, Paris, France (GRID:grid.168010.e); Directors’ research, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany (GRID:grid.4709.a) (ISNI:0000 0004 0495 846X); Collège de France, Paris, France (GRID:grid.410533.0) (ISNI:0000 0001 2179 2236) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2570656889
Copyright
© The Author(s) 2021. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.