FBRSL1 couples ncPRC1.3 to CoREST to repress cell-cycle genes during human neuronal differentiation
- 1University of Miami
Abstract
Most Polycomb complexes foster canonical gene repression, while noncanonical PRC1.3 (ncPRC1.3) unexpectedly activates transcription through its AUTS2 component. If and how ncPRC1.3 may also foster gene repression during development is unknown. Here, we show that in contrast to the impact of AUTS2 on ncPRC1.3, its paralog, FBRSL1, couples ncPRC1.3 to the CoREST/CTBP/LSD1 corepressor complex to mediate transcriptional repression. AUTS2 and FBRSL1 compete for binding to the RAWUL domain of the ncPRC1.3 subunit, PCGF3, and their isolated Atrophin-1 domains confer opposite transcriptional outputs. Corepressor interaction maps to a central Atrophin-1-containing region of FBRSL1, with CoREST and CTBP2 required for reporter repression. Patient-derived FBRSL1 truncations abolish this repressive capacity; specifically, the p.Gln163* variant retains PCGF3 binding, but loses corepressor association. In human embryonic stem cells carrying a homozygous p.Gln163* knock-in, cortical differentiation displays persistent cell-cycle gene expression and deficient neuronal gene induction. At the progenitor stage, chromatin occupancy of CoREST, CTBP2, PCGF3, and RING1B is lost and accessibility increases at cell-cycle promoters that subsequently fail to be repressed. Thus, FBRSL1 redirects ncPRC1.3 function by equipping the complex with a corepressor-linked repressive arm that restrains proliferative programs at the progenitor-to-neuron transition.
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BibTeX
@misc{liu2026fbrsl1,
title = {{FBRSL1 couples ncPRC1.3 to CoREST to repress cell-cycle genes during human neuronal differentiation}},
author = {S. Liu and H.-W. Chang and D. Reinberg},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.20.760506},
url = {https://www.biorxiv.org/content/10.64898/2026.10.20.760506v1},
note = {CC BY-NC},
}
RIS
TY - UNPB
TI - FBRSL1 couples ncPRC1.3 to CoREST to repress cell-cycle genes during human neuronal differentiation
AU - S. Liu
AU - H.-W. Chang
AU - D. Reinberg
PY - 2026
DA - 2026/10/20
PB - bioRxiv
DO - 10.64898/2026.10.20.760506
UR - https://www.biorxiv.org/content/10.64898/2026.10.20.760506v1
AB - Most Polycomb complexes foster canonical gene repression, while noncanonical PRC1.3 (ncPRC1.3) unexpectedly activates transcription through its AUTS2 component. If and how ncPRC1.3 may also foster gene repression during development is unknown. Here, we show that in contrast to the impact of AUTS2 on ncPRC1.3, its paralog, FBRSL1, couples ncPRC1.3 to the CoREST/CTBP/LSD1 corepressor complex to mediate transcriptional repression. AUTS2 and FBRSL1 compete for binding to the RAWUL domain of the ncPRC1.3 subunit, PCGF3, and their isolated Atrophin-1 domains confer opposite transcriptional outputs. Corepressor interaction maps to a central Atrophin-1-containing region of FBRSL1, with CoREST and CTBP2 required for reporter repression. Patient-derived FBRSL1 truncations abolish this repressive capacity; specifically, the p.Gln163* variant retains PCGF3 binding, but loses corepressor association. In human embryonic stem cells carrying a homozygous p.Gln163* knock-in, cortical differentiation displays persistent cell-cycle gene expression and deficient neuronal gene induction. At the progenitor stage, chromatin occupancy of CoREST, CTBP2, PCGF3, and RING1B is lost and accessibility increases at cell-cycle promoters that subsequently fail to be repressed. Thus, FBRSL1 redirects ncPRC1.3 function by equipping the complex with a corepressor-linked repressive arm that restrains proliferative programs at the progenitor-to-neuron transition.
ER -