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USP4 regulates ribosome biogenesis and protein synthesis for hematopoietic stem cell regeneration and leukemia progression. | LitMetric

USP4 regulates ribosome biogenesis and protein synthesis for hematopoietic stem cell regeneration and leukemia progression.

Leukemia

Key Laboratory of Regenerative Medicine of Ministry of Education, Institute of Aging and Regenerative Medicine, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.

Published: November 2024

AI Article Synopsis

  • Enhanced ribosome biogenesis and protein synthesis are essential for the rapid proliferation of hematopoietic stem cells (HSCs) during regeneration, but the mechanisms regulating this process are not fully understood.
  • The study identifies USP4 as a key player that is significantly upregulated in proliferating HSCs, influencing ribosome biogenesis and protein synthesis.
  • Deleting or inhibiting Usp4 reduces protein synthesis and HSC functionality, while also showing potential as a therapeutic approach to prolong survival in acute myeloid leukemia (AML) models.

Article Abstract

Enhanced ribosome biogenesis and protein synthesis are required for cell proliferation. During hematopoietic regeneration, hematopoietic stem cells (HSCs) proliferate rapidly to replenish the hematopoietic system. How HSCs respond and regulate ribosome biogenesis and protein synthesis during regeneration remains unclear. Here, we analyzed the expression of a series of ubiquitin-specific-proteases (USPs) during HSC regeneration. We found USP4 expression is significantly increased in proliferating HSCs. Further functional and mechanistic investigations revealed a crucial regulatory function of USP4 in HSC regeneration and leukemia progression by modulating ribosome biogenesis and protein synthesis. USP4 deubiquitinates and stabilizes PES1 to facilitate ribosome biogenesis and protein synthesis in proliferative HSCs and leukemic cells. Usp4 deletion significantly decreases protein synthesis, proliferation and reconstitution capacity of HSCs. Usp4 inhibition suppresses ribosome biogenesis and proliferation of leukemic cells, and prolongs the survival of AML (Acute myeloid leukemia) mice. These findings provide a new insight into the response mechanism of ribosome biogenesis and protein synthesis in HSCs, and their contribution to leukemia progression.

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Source
http://dx.doi.org/10.1038/s41375-024-02338-zDOI Listing

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