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Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane

Members of the Oxa1/YidC/Alb3 protein family are involved in the insertion, folding, and assembly of membrane proteins in mitochondria, bacteria, and chloroplasts. The thylakoid membrane protein Alb3 mediates the chloroplast signal recognition particle (cpSRP)-dependent posttranslational insertion o...

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Autores principales: Ackermann, Bernd, Dünschede, Beatrix, Pietzenuk, Björn, Justesen, Bo Højen, Krämer, Ute, Hofmann, Eckhard, Günther Pomorski, Thomas, Schünemann, Danja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733628/
https://www.ncbi.nlm.nih.gov/pubmed/35003166
http://dx.doi.org/10.3389/fpls.2021.781857
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author Ackermann, Bernd
Dünschede, Beatrix
Pietzenuk, Björn
Justesen, Bo Højen
Krämer, Ute
Hofmann, Eckhard
Günther Pomorski, Thomas
Schünemann, Danja
author_facet Ackermann, Bernd
Dünschede, Beatrix
Pietzenuk, Björn
Justesen, Bo Højen
Krämer, Ute
Hofmann, Eckhard
Günther Pomorski, Thomas
Schünemann, Danja
author_sort Ackermann, Bernd
collection PubMed
description Members of the Oxa1/YidC/Alb3 protein family are involved in the insertion, folding, and assembly of membrane proteins in mitochondria, bacteria, and chloroplasts. The thylakoid membrane protein Alb3 mediates the chloroplast signal recognition particle (cpSRP)-dependent posttranslational insertion of nuclear-encoded light harvesting chlorophyll a/b-binding proteins and participates in the biogenesis of plastid-encoded subunits of the photosynthetic complexes. These subunits are cotranslationally inserted into the thylakoid membrane, yet very little is known about the molecular mechanisms underlying docking of the ribosome-nascent chain complexes to the chloroplast SecY/Alb3 insertion machinery. Here, we show that nanodisc-embedded Alb3 interacts with ribosomes, while the homolog Alb4, also located in the thylakoid membrane, shows no ribosome binding. Alb3 contacts the ribosome with its C-terminal region and at least one additional binding site within its hydrophobic core region. Within the C-terminal region, two conserved motifs (motifs III and IV) are cooperatively required to enable the ribosome contact. Furthermore, our data suggest that the negatively charged C-terminus of the ribosomal subunit uL4c is involved in Alb3 binding. Phylogenetic analyses of uL4 demonstrate that this region newly evolved in the green lineage during the transition from aquatic to terrestrial life.
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spelling pubmed-87336282022-01-07 Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane Ackermann, Bernd Dünschede, Beatrix Pietzenuk, Björn Justesen, Bo Højen Krämer, Ute Hofmann, Eckhard Günther Pomorski, Thomas Schünemann, Danja Front Plant Sci Plant Science Members of the Oxa1/YidC/Alb3 protein family are involved in the insertion, folding, and assembly of membrane proteins in mitochondria, bacteria, and chloroplasts. The thylakoid membrane protein Alb3 mediates the chloroplast signal recognition particle (cpSRP)-dependent posttranslational insertion of nuclear-encoded light harvesting chlorophyll a/b-binding proteins and participates in the biogenesis of plastid-encoded subunits of the photosynthetic complexes. These subunits are cotranslationally inserted into the thylakoid membrane, yet very little is known about the molecular mechanisms underlying docking of the ribosome-nascent chain complexes to the chloroplast SecY/Alb3 insertion machinery. Here, we show that nanodisc-embedded Alb3 interacts with ribosomes, while the homolog Alb4, also located in the thylakoid membrane, shows no ribosome binding. Alb3 contacts the ribosome with its C-terminal region and at least one additional binding site within its hydrophobic core region. Within the C-terminal region, two conserved motifs (motifs III and IV) are cooperatively required to enable the ribosome contact. Furthermore, our data suggest that the negatively charged C-terminus of the ribosomal subunit uL4c is involved in Alb3 binding. Phylogenetic analyses of uL4 demonstrate that this region newly evolved in the green lineage during the transition from aquatic to terrestrial life. Frontiers Media S.A. 2021-12-23 /pmc/articles/PMC8733628/ /pubmed/35003166 http://dx.doi.org/10.3389/fpls.2021.781857 Text en Copyright © 2021 Ackermann, Dünschede, Pietzenuk, Justesen, Krämer, Hofmann, Günther Pomorski and Schünemann. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Ackermann, Bernd
Dünschede, Beatrix
Pietzenuk, Björn
Justesen, Bo Højen
Krämer, Ute
Hofmann, Eckhard
Günther Pomorski, Thomas
Schünemann, Danja
Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane
title Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane
title_full Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane
title_fullStr Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane
title_full_unstemmed Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane
title_short Chloroplast Ribosomes Interact With the Insertase Alb3 in the Thylakoid Membrane
title_sort chloroplast ribosomes interact with the insertase alb3 in the thylakoid membrane
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733628/
https://www.ncbi.nlm.nih.gov/pubmed/35003166
http://dx.doi.org/10.3389/fpls.2021.781857
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