Paper

Regulation of human development by ubiquitin chain editing of chromatin remodelers

Asmar, Anthony J, Aksentijevich, Ivona, Saida, Ken, Bodurtha, Joann, Undiagnosed Diseases Network, Walkiewicz, Magdalena, Ryan, Dale, Nishimura, Yutaka, Uehara, Daniela T, Okada, Satoshi, Kosho, Tomoki, Kempers, Marlies, Mitra, Apratim, Baranano, Kristin W, Wang, Raymond, Rocha, Pedro P, Miyake, Noriko, Macnamara, Ellen, Werner, Achim, Beck, David, Oda, Hirotsugu, Mu, Weiyi, Matsumoto, Naomichi, Inazawa, Johi, Tifft, Cynthia J, Thompson, Joyce, Kastner, Daniel L, Souza, Precilla D, Basar, Mohammed A

2020

Overview

Embryonic development occurs through commitment of pluripotent stem cells to differentiation programs that require highly coordinated changes in gene expression. Chromatin remodeling of gene regulatory elements is a critical component of how such changes are achieved. While many factors controlling chromatin dynamics are known, mechanisms of how different chromatin regulators are orchestrated during development are not well understood. Here, we describe LINKED (LINKage-specific-deubiquitylation-deficiency-induced Embryonic Defects) syndrome, a novel multiple congenital anomaly disorder caused by hypomorphic hemizygous missense variants in the deubiquitylase OTUD5/DUBA. Studying LINKED mutations in vitro, in mouse, and in models of neuroectodermal differentiation of human pluripotent stem cells, we uncover a novel regulatory circuit that coordinates chromatin remodeling pathways during early differentiation. We show that the K48-linkage-specific deubiquitylation activity of OTUD5 is essential for murine and human development and, if reduced, leads to aberrant cell-fate specification. OTUD5 controls differentiation through preventing the degradation of multiple chromatin regulators including ARID1A/B and HDAC2, mutation of which underlie developmental syndromes that exhibit phenotypic overlap with LINKED patients. Accordingly, loss of OTUD5 during early differentiation leads to less accessible chromatin at neural and neural crest enhancers and thus aberrant rewiring of gene expression networks. Our work identifies a novel mechanistic link between phenotypically related developmental disorders and an essential function for linkage-specific ubiquitin editing of substrate groups (i.e. chromatin remodeling complexes) during early cell-fate decisions; a regulatory concept, we predict to be a general feature of embryonic development.

• Publisher: Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
• Subject: Animal models / Cell differentiation / Chromatin remodeling / Developmental disabilities / Embryogenesis / Enhancers / Gene expression / Genetics / HDAC2 protein / Histone deacetylase / Mutation / Neural crest / Pluripotency / Regulatory sequences / Stem cell transplantation / Stem cells / Ubiquitin