Notch-induced endoplasmic reticulum-associated degradation governs mouse thymocyte β-selection.

ABSTRACT: Signals from the pre-T cell receptor and Notch coordinately instruct β-selection of CD4^-CD8^-double negative (DN) thymocytes to generate αβ T cells in the thymus. However, how these signals ensure a high-fidelity proteome and safeguard the clonal diversification of the pre-selection TCR repertoire given the considerable translational activity imposed by β-selection is largely unknown. Here, we identify the endoplasmic reticulum (ER)-associated degradation (ERAD) machinery as a critical proteostasis checkpoint during β-selection. Expression of the SEL1L-HRD1 complex, the most conserved branch of ERAD, is directly regulated by the transcriptional activity of the Notch intracellular domain. Deletion of Sel1l impaired DN3 to DN4 thymocyte transition and severely imp

SUBMITTER: Liu X 

PROVIDER: S-EPMC8315795 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature