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A Comprehensive Enumeration of the Human Proteostasis Network. 1. Components of Translation, Protein Folding, and Organelle-Specific Systems

The Proteostasis Consortium, Overall coordination,Suzanne Elsasser,Lisa P. Elia,Richard I. Morimoto,Evan T. Powers, Harvard Medical School group (analysis),Daniel Finley,University of California, San Francisco and Gladstone Institutes group I (chaperones, analysis),Eric Mockler,Leandro Lima,Steve Finkbeiner,University of California, San Francisco group II (chaperones, analysis),Jason E. Gestwicki, Northwestern University group (chaperones, analysis),Thomas Stoeger, Kedi Cao, The Scripps Research Institute group (chaperones, endoplasmic reticulum proteostasis, mitochondrial proteostasis, analysis),Dan Garza,Jeffery W. Kelly, Stanford University group (chaperones, translation, mitochondrial proteostasis),Miranda Collier,T. Kelly Rainbolt,Shuhei Taguwa,Ching-Chieh Chou,Ranen Aviner,Natália Barbosa,Fabián Morales-Polanco,Vincent B. Masto,Judith Frydman

biorxiv(2022)

Cited 8|Views40
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Abstract
The condition of having a healthy, functional proteome is known as protein homeostasis, or proteostasis. Establishing and maintaining proteostasis is the province of the proteostasis network, approximately 2,500 genes that regulate protein synthesis, folding, localization, and degradation. The proteostasis network is a fundamental entity in biology with direct relevance to many diseases of protein conformation. However, it is not well defined or annotated, which hinders its functional characterization in health and disease. In this series of manuscripts, we aim to operationally define the human proteostasis network by providing a comprehensive, annotated list of its components. Here, we provide a curated list of 959 unique genes that comprise the protein synthesis machinery, chaperones, folding enzymes, systems for trafficking proteins into and out of organelles, and organelle-specific degradation systems. In subsequent manuscripts, we will delineate the human autophagy-lysosome pathway, the ubiquitin-proteasome system, and the proteostasis networks of model organisms. ### Competing Interest Statement The authors have declared no competing interest.
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