Cargando…

Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head

The correct assembly of ribosomes from ribosomal RNAs (rRNAs) and ribosomal proteins (RPs) is critical, as indicated by the diseases caused by RP haploinsufficiency and loss of RP stoichiometry in cancer cells. Nevertheless, how assembly of each RP is ensured remains poorly understood. We use yeast...

Descripción completa

Detalles Bibliográficos
Autores principales: Collins, Jason C., Ghalei, Homa, Doherty, Joanne R., Huang, Haina, Culver, Rebecca N., Karbstein, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279377/
https://www.ncbi.nlm.nih.gov/pubmed/30348748
http://dx.doi.org/10.1083/jcb.201804163
_version_ 1783378493642375168
author Collins, Jason C.
Ghalei, Homa
Doherty, Joanne R.
Huang, Haina
Culver, Rebecca N.
Karbstein, Katrin
author_facet Collins, Jason C.
Ghalei, Homa
Doherty, Joanne R.
Huang, Haina
Culver, Rebecca N.
Karbstein, Katrin
author_sort Collins, Jason C.
collection PubMed
description The correct assembly of ribosomes from ribosomal RNAs (rRNAs) and ribosomal proteins (RPs) is critical, as indicated by the diseases caused by RP haploinsufficiency and loss of RP stoichiometry in cancer cells. Nevertheless, how assembly of each RP is ensured remains poorly understood. We use yeast genetics, biochemistry, and structure probing to show that the assembly factor Ltv1 facilitates the incorporation of Rps3, Rps10, and Asc1/RACK1 into the small ribosomal subunit head. Ribosomes from Ltv1-deficient yeast have substoichiometric amounts of Rps10 and Asc1 and show defects in translational fidelity and ribosome-mediated RNA quality control. These defects provide a growth advantage under some conditions but sensitize the cells to oxidative stress. Intriguingly, relative to glioma cell lines, breast cancer cells have reduced levels of LTV1 and produce ribosomes lacking RPS3, RPS10, and RACK1. These data describe a mechanism to ensure RP assembly and demonstrate how cancer cells circumvent this mechanism to generate diverse ribosome populations that can promote survival under stress.
format Online
Article
Text
id pubmed-6279377
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-62793772019-06-03 Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head Collins, Jason C. Ghalei, Homa Doherty, Joanne R. Huang, Haina Culver, Rebecca N. Karbstein, Katrin J Cell Biol Research Articles The correct assembly of ribosomes from ribosomal RNAs (rRNAs) and ribosomal proteins (RPs) is critical, as indicated by the diseases caused by RP haploinsufficiency and loss of RP stoichiometry in cancer cells. Nevertheless, how assembly of each RP is ensured remains poorly understood. We use yeast genetics, biochemistry, and structure probing to show that the assembly factor Ltv1 facilitates the incorporation of Rps3, Rps10, and Asc1/RACK1 into the small ribosomal subunit head. Ribosomes from Ltv1-deficient yeast have substoichiometric amounts of Rps10 and Asc1 and show defects in translational fidelity and ribosome-mediated RNA quality control. These defects provide a growth advantage under some conditions but sensitize the cells to oxidative stress. Intriguingly, relative to glioma cell lines, breast cancer cells have reduced levels of LTV1 and produce ribosomes lacking RPS3, RPS10, and RACK1. These data describe a mechanism to ensure RP assembly and demonstrate how cancer cells circumvent this mechanism to generate diverse ribosome populations that can promote survival under stress. Rockefeller University Press 2018-12-03 /pmc/articles/PMC6279377/ /pubmed/30348748 http://dx.doi.org/10.1083/jcb.201804163 Text en © 2018 Collins et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Collins, Jason C.
Ghalei, Homa
Doherty, Joanne R.
Huang, Haina
Culver, Rebecca N.
Karbstein, Katrin
Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head
title Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head
title_full Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head
title_fullStr Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head
title_full_unstemmed Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head
title_short Ribosome biogenesis factor Ltv1 chaperones the assembly of the small subunit head
title_sort ribosome biogenesis factor ltv1 chaperones the assembly of the small subunit head
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279377/
https://www.ncbi.nlm.nih.gov/pubmed/30348748
http://dx.doi.org/10.1083/jcb.201804163
work_keys_str_mv AT collinsjasonc ribosomebiogenesisfactorltv1chaperonestheassemblyofthesmallsubunithead
AT ghaleihoma ribosomebiogenesisfactorltv1chaperonestheassemblyofthesmallsubunithead
AT dohertyjoanner ribosomebiogenesisfactorltv1chaperonestheassemblyofthesmallsubunithead
AT huanghaina ribosomebiogenesisfactorltv1chaperonestheassemblyofthesmallsubunithead
AT culverrebeccan ribosomebiogenesisfactorltv1chaperonestheassemblyofthesmallsubunithead
AT karbsteinkatrin ribosomebiogenesisfactorltv1chaperonestheassemblyofthesmallsubunithead