Elongational stalling activates mitoribosome-associated quality control

Author:

Desai Nirupa1ORCID,Yang Hanting1ORCID,Chandrasekaran Viswanathan1ORCID,Kazi Razina1ORCID,Minczuk Michal2,Ramakrishnan V.1ORCID

Affiliation:

1. MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

2. MRC Mitochondrial Biology Unit, University of Cambridge, Hills Road, Cambridge CB2 0XY, UK.

Abstract

Quality control in mitochondria Human mitochondria have their own genome and ribosomes called mitoribosomes that respectively encode and synthesize essential subunits of complexes that use the energy from the oxidation of metabolites to drive the synthesis of adenosine triphosphate (ATP). These complexes are key to the health of the cell. Desai et al. studied a mitoribosome-associated quality control pathway that prevents aberrant translation. They purified mitoribosomes under conditions designed to induce stalling and determined the structures of two intermediates in the rescue pathway. These structures revealed two proteins that eject the unfinished polypeptide chain and peptidyl transfer RNA from the ribosome. Their cryo–electron microscopy dataset also revealed additional states that may correspond to intermediates in the mitochondrial translation elongation cycle. Science , this issue p. 1105

Funder

European Molecular Biology Organization

Agouron Institute

Wellcome

Medical Research Council

Louis-Jeantet Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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