Disruption of the chaperonin containing TCP-1 function affects protein networks essential for rod outer segment morphogenesis and survival

Ekaterina Posokhova, Hongman Song, Marycharmain Belcastro, Lee Ann Higgins, Lauren R. Bigley, Norman A. Michaud, Kirill A. Martemyanov, Maxim Sokolov

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

Type II Chaperonin Containing TCP-1 (CCT, also known as TCP-1 Ring Complex, TRiC) is a multi-subunit molecular machine thought to assist in the folding of ∼10% of newly translated cytosolic proteins in eukaryotes. A number of proteins folded by CCT have been identified in yeast and cultured mammalian cells, however, the function of this chaperonin in vivo has never been addressed. Here we demonstrate that suppressing the CCT activity in mouse photoreceptors by transgenic expression of a dominant-negative mutant of the CCT cofactor, phosducin-like protein (PhLP), results in the malformation of the outer segment, a cellular compartment responsible for light detection, and triggers rapid retinal degeneration. Investigation of the underlying causes by quantitative proteomics identified distinct protein networks, encompassing ∼200 proteins, which were significantly affected by the chaperonin deficiency. Notably among those were several essential proteins crucially engaged in structural support and visual signaling of the outer segment such as peripherin 2, Rom1, rhodopsin, transducin, and PDE6. These data for the first time demonstrate that normal CCT function is ultimately required for the morphogenesis and survival of sensory neurons of the retina, and suggest the chaperonin CCT deficiency as a potential, yet unexplored, cause of neurodegenerative diseases.

Original languageEnglish (US)
JournalMolecular and Cellular Proteomics
Volume10
Issue number1
DOIs
StatePublished - Jan 2011

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