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Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis

Each day, about 10(12) erythrocytes and platelets are released into the bloodstream. This substantial output from hematopoietic stem cells is tightly regulated by transcriptional and epigenetic factors. Whether and how circular RNAs (circRNAs) contribute to the differentiation and/or identity of hem...

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Autores principales: Nicolet, Benoit P., Jansen, Sjoert B.G., Heideveld, Esther, Ouwehand, Willem H., van den Akker, Emile, von Lindern, Marieke, Wolkers, Monika C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906552/
https://www.ncbi.nlm.nih.gov/pubmed/34732567
http://dx.doi.org/10.1261/rna.078754.121
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author Nicolet, Benoit P.
Jansen, Sjoert B.G.
Heideveld, Esther
Ouwehand, Willem H.
van den Akker, Emile
von Lindern, Marieke
Wolkers, Monika C.
author_facet Nicolet, Benoit P.
Jansen, Sjoert B.G.
Heideveld, Esther
Ouwehand, Willem H.
van den Akker, Emile
von Lindern, Marieke
Wolkers, Monika C.
author_sort Nicolet, Benoit P.
collection PubMed
description Each day, about 10(12) erythrocytes and platelets are released into the bloodstream. This substantial output from hematopoietic stem cells is tightly regulated by transcriptional and epigenetic factors. Whether and how circular RNAs (circRNAs) contribute to the differentiation and/or identity of hematopoietic cells is to date not known. We recently reported that erythrocytes and platelets contain the highest levels and numbers of circRNAs among hematopoietic cells. Here, we provide the first detailed analysis of circRNA expression during erythroid and megakaryoid differentiation. CircRNA expression not only significantly increased upon enucleation, but also had limited overlap between progenitor cells and mature cells, suggesting that circRNA expression stems from regulated processes rather than resulting from mere accumulation. To study circRNA function in hematopoiesis, we first compared the expression levels of circRNAs with the translation efficiency of their mRNA counterpart. We found that only one out of 2531 (0.04%) circRNAs associated with mRNA-translation regulation. Furthermore, irrespective of thousands of identified putative open reading frames, deep ribosome-footprinting sequencing, and mass spectrometry analysis provided little evidence for translation of endogenously expressed circRNAs. In conclusion, circRNAs alter their expression profile during terminal hematopoietic differentiation, yet their contribution to regulate cellular processes remains enigmatic.
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spelling pubmed-89065522022-03-23 Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis Nicolet, Benoit P. Jansen, Sjoert B.G. Heideveld, Esther Ouwehand, Willem H. van den Akker, Emile von Lindern, Marieke Wolkers, Monika C. RNA Article Each day, about 10(12) erythrocytes and platelets are released into the bloodstream. This substantial output from hematopoietic stem cells is tightly regulated by transcriptional and epigenetic factors. Whether and how circular RNAs (circRNAs) contribute to the differentiation and/or identity of hematopoietic cells is to date not known. We recently reported that erythrocytes and platelets contain the highest levels and numbers of circRNAs among hematopoietic cells. Here, we provide the first detailed analysis of circRNA expression during erythroid and megakaryoid differentiation. CircRNA expression not only significantly increased upon enucleation, but also had limited overlap between progenitor cells and mature cells, suggesting that circRNA expression stems from regulated processes rather than resulting from mere accumulation. To study circRNA function in hematopoiesis, we first compared the expression levels of circRNAs with the translation efficiency of their mRNA counterpart. We found that only one out of 2531 (0.04%) circRNAs associated with mRNA-translation regulation. Furthermore, irrespective of thousands of identified putative open reading frames, deep ribosome-footprinting sequencing, and mass spectrometry analysis provided little evidence for translation of endogenously expressed circRNAs. In conclusion, circRNAs alter their expression profile during terminal hematopoietic differentiation, yet their contribution to regulate cellular processes remains enigmatic. Cold Spring Harbor Laboratory Press 2022-02 /pmc/articles/PMC8906552/ /pubmed/34732567 http://dx.doi.org/10.1261/rna.078754.121 Text en © 2022 Nicolet et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Article
Nicolet, Benoit P.
Jansen, Sjoert B.G.
Heideveld, Esther
Ouwehand, Willem H.
van den Akker, Emile
von Lindern, Marieke
Wolkers, Monika C.
Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
title Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
title_full Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
title_fullStr Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
title_full_unstemmed Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
title_short Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
title_sort circular rnas exhibit limited evidence for translation, or translation regulation of the mrna counterpart in terminal hematopoiesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906552/
https://www.ncbi.nlm.nih.gov/pubmed/34732567
http://dx.doi.org/10.1261/rna.078754.121
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