SMARCAD1 ATPase activity is required to silence endogenous retroviruses in embryonic stem cells
Philipps University of Marburg · Institute of Molecular Biology
Abstract
Endogenous retroviruses (ERVs) can confer benefits to their host but present a threat to genome integrity if not regulated correctly. Here we identify the SWI/SNF-like remodeler SMARCAD1 as a key factor in the control of ERVs in embryonic stem cells. SMARCAD1 is enriched at ERV subfamilies class I and II, particularly at active intracisternal A-type particles (IAPs), where it preserves repressive histone methylation marks. Depletion of SMARCAD1 results in de-repression of IAPs and adjacent genes. Recruitment of SMARCAD1 to ERVs is dependent on KAP1, a central component of the silencing machinery. SMARCAD1 and KAP1 occupancy at ERVs is co-dependent and requires the ATPase function of SMARCAD1. Our findings…
Citation impact
- FWCI
- 473.16
- Percentile
- 100%
- References
- 71
Authors
9- PSParysatis SachsCorresponding
Philipps University of Marburg, Institute of Molecular Biology
- DDDong Ding
Philipps University of Marburg, Institute of Molecular Biology
- PBPhilipp Bergmaier
Philipps University of Marburg, Institute of Molecular Biology
- BLBoris Lamp
Philipps University of Marburg
- CSChristina Schlagheck
Philipps University of Marburg, Institute of Molecular Biology
Topics & keywords
- Endogenous retrovirus
- Retrotransposon
- Chromatin
- Biology
- Histone
- Embryonic stem cell
- Epigenetics
- Genome