Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA

Using a modified RNA-sequencing (RNA-seq) approach, we discovered a new family of unusually short RNAs mapping to ribosomal RNA 5.8S, which we named dodecaRNAs (doRNAs), according to the number of core nucleotides (12 nt) their members contain. Using a new quantitative detection method that we devel...

Full description

Bibliographic Details
Main Authors: Marine Lambert, Abderrahim Benmoussa, Idrissa Diallo, Katheryn Ouellet-Boutin, Véronique Dorval, Nathalie Majeau, Charles Joly-Beauparlant, Arnaud Droit, Alain Bergeron, Bernard Têtu, Yves Fradet, Frédéric Pouliot, Patrick Provost
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/18/9757
_version_ 1797518970212843520
author Marine Lambert
Abderrahim Benmoussa
Idrissa Diallo
Katheryn Ouellet-Boutin
Véronique Dorval
Nathalie Majeau
Charles Joly-Beauparlant
Arnaud Droit
Alain Bergeron
Bernard Têtu
Yves Fradet
Frédéric Pouliot
Patrick Provost
author_facet Marine Lambert
Abderrahim Benmoussa
Idrissa Diallo
Katheryn Ouellet-Boutin
Véronique Dorval
Nathalie Majeau
Charles Joly-Beauparlant
Arnaud Droit
Alain Bergeron
Bernard Têtu
Yves Fradet
Frédéric Pouliot
Patrick Provost
author_sort Marine Lambert
collection DOAJ
description Using a modified RNA-sequencing (RNA-seq) approach, we discovered a new family of unusually short RNAs mapping to ribosomal RNA 5.8S, which we named dodecaRNAs (doRNAs), according to the number of core nucleotides (12 nt) their members contain. Using a new quantitative detection method that we developed, we confirmed our RNA-seq data and determined that the minimal core doRNA sequence and its 13-nt variant C-doRNA (doRNA with a 5′ Cytosine) are the two most abundant doRNAs, which, together, may outnumber microRNAs. The C-doRNA/doRNA ratio is stable within species but differed between species. doRNA and C-doRNA are mainly cytoplasmic and interact with heterogeneous nuclear ribonucleoproteins (hnRNP) A0, A1 and A2B1, but not Argonaute 2. Reporter gene activity assays suggest that C-doRNA may function as a regulator of Annexin II receptor (AXIIR) expression. doRNAs are differentially expressed in prostate cancer cells/tissues and may control cell migration. These findings suggest that unusually short RNAs may be more abundant and important than previously thought.
first_indexed 2024-03-10T07:35:48Z
format Article
id doaj.art-778f942ddc6a4232b45aa9de2ba5ab73
institution Directory Open Access Journal
issn 1661-6596
1422-0067
language English
last_indexed 2024-03-10T07:35:48Z
publishDate 2021-09-01
publisher MDPI AG
record_format Article
series International Journal of Molecular Sciences
spelling doaj.art-778f942ddc6a4232b45aa9de2ba5ab732023-11-22T13:27:04ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-09-012218975710.3390/ijms22189757Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNAMarine Lambert0Abderrahim Benmoussa1Idrissa Diallo2Katheryn Ouellet-Boutin3Véronique Dorval4Nathalie Majeau5Charles Joly-Beauparlant6Arnaud Droit7Alain Bergeron8Bernard Têtu9Yves Fradet10Frédéric Pouliot11Patrick Provost12CHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaCHU de Québec Research Center/CHUL Pavilion—Université Laval, 2705 boulevard Laurier, Quebec City, QC G1V 4G2, CanadaUsing a modified RNA-sequencing (RNA-seq) approach, we discovered a new family of unusually short RNAs mapping to ribosomal RNA 5.8S, which we named dodecaRNAs (doRNAs), according to the number of core nucleotides (12 nt) their members contain. Using a new quantitative detection method that we developed, we confirmed our RNA-seq data and determined that the minimal core doRNA sequence and its 13-nt variant C-doRNA (doRNA with a 5′ Cytosine) are the two most abundant doRNAs, which, together, may outnumber microRNAs. The C-doRNA/doRNA ratio is stable within species but differed between species. doRNA and C-doRNA are mainly cytoplasmic and interact with heterogeneous nuclear ribonucleoproteins (hnRNP) A0, A1 and A2B1, but not Argonaute 2. Reporter gene activity assays suggest that C-doRNA may function as a regulator of Annexin II receptor (AXIIR) expression. doRNAs are differentially expressed in prostate cancer cells/tissues and may control cell migration. These findings suggest that unusually short RNAs may be more abundant and important than previously thought.https://www.mdpi.com/1422-0067/22/18/9757RNA sequencingsmall RNAnon-coding RNART-qPCR5.8S rRNA
spellingShingle Marine Lambert
Abderrahim Benmoussa
Idrissa Diallo
Katheryn Ouellet-Boutin
Véronique Dorval
Nathalie Majeau
Charles Joly-Beauparlant
Arnaud Droit
Alain Bergeron
Bernard Têtu
Yves Fradet
Frédéric Pouliot
Patrick Provost
Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA
International Journal of Molecular Sciences
RNA sequencing
small RNA
non-coding RNA
RT-qPCR
5.8S rRNA
title Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA
title_full Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA
title_fullStr Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA
title_full_unstemmed Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA
title_short Identification of Abundant and Functional dodecaRNAs (doRNAs) Derived from Ribosomal RNA
title_sort identification of abundant and functional dodecarnas dornas derived from ribosomal rna
topic RNA sequencing
small RNA
non-coding RNA
RT-qPCR
5.8S rRNA
url https://www.mdpi.com/1422-0067/22/18/9757
work_keys_str_mv AT marinelambert identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT abderrahimbenmoussa identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT idrissadiallo identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT katherynouelletboutin identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT veroniquedorval identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT nathaliemajeau identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT charlesjolybeauparlant identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT arnauddroit identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT alainbergeron identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT bernardtetu identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT yvesfradet identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT fredericpouliot identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna
AT patrickprovost identificationofabundantandfunctionaldodecarnasdornasderivedfromribosomalrna