A Comprehensive Enumeration of the Human Proteostasis Network. 1. Components of Translation, Protein Folding, and Organelle-Specific Systems
The Proteostasis Consortium, ; Elsasser, S.; Finley, D.; Mockler, E.; Lima, L.; Finkbeiner, S.; Gestwicki, J. E.; Stoeger, T. E.; Cao, K.; Garza, D.; Kelly, J. W.; Collier, M.; Rainbolt, T. K.; Taguwa, S.; Chou, C.-C.; Aviner, R.; Barbosa, N.; Moralez-Polanco, F.; Masto, V. B.; Frydman, J.; Elia, L. P.; Morimoto, R. I.; Powers, E. T.
Show 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.
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