| Literature DB >> 33186096 |
Iromi Wanigasuriya1,2, Quentin Gouil1,2, Sarah A Kinkel1,2, Andrés Tapia Del Fierro1,2, Tamara Beck1, Ellise A Roper3, Kelsey Breslin1, Jessica Stringer4, Karla Hutt4, Heather J Lee3, Andrew Keniry1,2, Matthew E Ritchie1,2,5, Marnie E Blewitt1,2.
Abstract
Genomic imprinting establishes parental allele-biased expression of a suite of mammalian genes based on parent-of-origin specific epigenetic marks. These marks are under the control of maternal effect proteins supplied in the oocyte. Here we report epigenetic repressor Smchd1 as a novel maternal effect gene that regulates the imprinted expression of ten genes in mice. We also found zygotic SMCHD1 had a dose-dependent effect on the imprinted expression of seven genes. Together, zygotic and maternal SMCHD1 regulate three classic imprinted clusters and eight other genes, including non-canonical imprinted genes. Interestingly, the loss of maternal SMCHD1 does not alter germline DNA methylation imprints pre-implantation or later in gestation. Instead, what appears to unite most imprinted genes sensitive to SMCHD1 is their reliance on polycomb-mediated methylation as germline or secondary imprints, therefore we propose that SMCHD1 acts downstream of polycomb imprints to mediate its function.Entities:
Keywords: H3K27me3 imprints; Smchd1; allele-specific gene expression; developmental biology; genetics; genomic imprinting; genomics; maternal effect gene; mouse
Year: 2020 PMID: 33186096 PMCID: PMC7665889 DOI: 10.7554/eLife.55529
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140