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Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish
Yeast Rcl1 is a potential endonuclease that mediates pre-RNA cleavage at the A(2)-site to separate 18S rRNA from 5.8S and 25S rRNAs. However, the biological function of Rcl1 in opisthokonta is poorly defined. Moreover, there is no information regarding the exact positions of 18S pre-rRNA processing...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191805/ https://www.ncbi.nlm.nih.gov/pubmed/34019640 http://dx.doi.org/10.1093/nar/gkab381 |
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author | Zhu, Qinfang Tao, Boxiang Chen, Hong Shi, Hui Huang, Ling Chen, Jun Hu, Minjie Lo, Li Jan Peng, Jinrong |
author_facet | Zhu, Qinfang Tao, Boxiang Chen, Hong Shi, Hui Huang, Ling Chen, Jun Hu, Minjie Lo, Li Jan Peng, Jinrong |
author_sort | Zhu, Qinfang |
collection | PubMed |
description | Yeast Rcl1 is a potential endonuclease that mediates pre-RNA cleavage at the A(2)-site to separate 18S rRNA from 5.8S and 25S rRNAs. However, the biological function of Rcl1 in opisthokonta is poorly defined. Moreover, there is no information regarding the exact positions of 18S pre-rRNA processing in zebrafish. Here, we report that zebrafish pre-rRNA harbours three major cleavage sites in the 5′ETS, namely –477nt (A′-site), –97nt (A(0)-site) and the 5′ETS and 18S rRNA link (A(1)-site), as well as two major cleavage regions within the ITS1, namely 208–218nt (site 2) and 20–33nt (site E). We also demonstrate that depletion of zebrafish Rcl1 mainly impairs cleavage at the A(1)-site. Phenotypically, rcl1(–/–) mutants exhibit a small liver and exocrine pancreas and die before 15 days post-fertilization. RNA-seq analysis revealed that the most significant event in rcl1(–/–) mutants is the up-regulated expression of a cohort of genes related to ribosome biogenesis and tRNA production. Our data demonstrate that Rcl1 is essential for 18S rRNA maturation at the A(1)-site and for digestive organogenesis in zebrafish. Rcl1 deficiency, similar to deficiencies in other ribosome biogenesis factors, might trigger a common mechanism to upregulate the expression of genes responsible for ribosome biogenesis. |
format | Online Article Text |
id | pubmed-8191805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81918052021-06-11 Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish Zhu, Qinfang Tao, Boxiang Chen, Hong Shi, Hui Huang, Ling Chen, Jun Hu, Minjie Lo, Li Jan Peng, Jinrong Nucleic Acids Res Molecular Biology Yeast Rcl1 is a potential endonuclease that mediates pre-RNA cleavage at the A(2)-site to separate 18S rRNA from 5.8S and 25S rRNAs. However, the biological function of Rcl1 in opisthokonta is poorly defined. Moreover, there is no information regarding the exact positions of 18S pre-rRNA processing in zebrafish. Here, we report that zebrafish pre-rRNA harbours three major cleavage sites in the 5′ETS, namely –477nt (A′-site), –97nt (A(0)-site) and the 5′ETS and 18S rRNA link (A(1)-site), as well as two major cleavage regions within the ITS1, namely 208–218nt (site 2) and 20–33nt (site E). We also demonstrate that depletion of zebrafish Rcl1 mainly impairs cleavage at the A(1)-site. Phenotypically, rcl1(–/–) mutants exhibit a small liver and exocrine pancreas and die before 15 days post-fertilization. RNA-seq analysis revealed that the most significant event in rcl1(–/–) mutants is the up-regulated expression of a cohort of genes related to ribosome biogenesis and tRNA production. Our data demonstrate that Rcl1 is essential for 18S rRNA maturation at the A(1)-site and for digestive organogenesis in zebrafish. Rcl1 deficiency, similar to deficiencies in other ribosome biogenesis factors, might trigger a common mechanism to upregulate the expression of genes responsible for ribosome biogenesis. Oxford University Press 2021-05-21 /pmc/articles/PMC8191805/ /pubmed/34019640 http://dx.doi.org/10.1093/nar/gkab381 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Zhu, Qinfang Tao, Boxiang Chen, Hong Shi, Hui Huang, Ling Chen, Jun Hu, Minjie Lo, Li Jan Peng, Jinrong Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
title | Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
title_full | Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
title_fullStr | Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
title_full_unstemmed | Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
title_short | Rcl1 depletion impairs 18S pre-rRNA processing at the A(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
title_sort | rcl1 depletion impairs 18s pre-rrna processing at the a(1)-site and up-regulates a cohort of ribosome biogenesis genes in zebrafish |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191805/ https://www.ncbi.nlm.nih.gov/pubmed/34019640 http://dx.doi.org/10.1093/nar/gkab381 |
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