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Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells

Excessive accumulation of embryonic stem cell (ESC)-specific microRNAs occurs in both ESCs and induced pluripotent stem cells (iPSC); yet, the mechanism involved is unknown. In iPSCs, we for the first time found that novel glycylated sugar alcohols, particularly glycylglycerins, are tightly bound wi...

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Autores principales: Chang-Lin, Samantha, Hung, Albert, Chang, Donald C., Lin, Yi-Wen, Ying, Shao-Yao, Lin, Shi-Lung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889939/
https://www.ncbi.nlm.nih.gov/pubmed/27001514
http://dx.doi.org/10.1093/nar/gkw186
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author Chang-Lin, Samantha
Hung, Albert
Chang, Donald C.
Lin, Yi-Wen
Ying, Shao-Yao
Lin, Shi-Lung
author_facet Chang-Lin, Samantha
Hung, Albert
Chang, Donald C.
Lin, Yi-Wen
Ying, Shao-Yao
Lin, Shi-Lung
author_sort Chang-Lin, Samantha
collection PubMed
description Excessive accumulation of embryonic stem cell (ESC)-specific microRNAs occurs in both ESCs and induced pluripotent stem cells (iPSC); yet, the mechanism involved is unknown. In iPSCs, we for the first time found that novel glycylated sugar alcohols, particularly glycylglycerins, are tightly bound with ESC-specific microRNA precursors (pre-miRNA), such as pre-miR-302. Among these isolated glycylglycerins, we further identified that 1,3-diglycylglycerin and 1,2,3-triglycylglycerin are two major compounds bonded with negatively charged nucleic acids via electro-affinity and subsequently forming sugar-like coats in the hairpin-like double helix structures of pre-miRNAs. As a result, such glycylglycerin-formed coating serves as a protection layer against miRNA degradation. Moreover, we found that the pH value of iPSC cytosol determines the charges of these glycylglycerins. During iPSC differentiation, the cytosol pH is increased and hence neutralizes the charges of glycylglycerins, consequently leading to fast miRNA degradation. Therefore, the current findings not only explain how ESC-specific miRNAs are preserved and accumulated in iPSCs and ESCs but also demonstrate an important function of glycylglycerins in protecting the structural integrity of highly degradable miRNAs, providing a useful means for maintaining miRNA/siRNA function as well as developing the related RNA interference (RNAi) applications.
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spelling pubmed-48899392016-06-06 Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells Chang-Lin, Samantha Hung, Albert Chang, Donald C. Lin, Yi-Wen Ying, Shao-Yao Lin, Shi-Lung Nucleic Acids Res RNA Excessive accumulation of embryonic stem cell (ESC)-specific microRNAs occurs in both ESCs and induced pluripotent stem cells (iPSC); yet, the mechanism involved is unknown. In iPSCs, we for the first time found that novel glycylated sugar alcohols, particularly glycylglycerins, are tightly bound with ESC-specific microRNA precursors (pre-miRNA), such as pre-miR-302. Among these isolated glycylglycerins, we further identified that 1,3-diglycylglycerin and 1,2,3-triglycylglycerin are two major compounds bonded with negatively charged nucleic acids via electro-affinity and subsequently forming sugar-like coats in the hairpin-like double helix structures of pre-miRNAs. As a result, such glycylglycerin-formed coating serves as a protection layer against miRNA degradation. Moreover, we found that the pH value of iPSC cytosol determines the charges of these glycylglycerins. During iPSC differentiation, the cytosol pH is increased and hence neutralizes the charges of glycylglycerins, consequently leading to fast miRNA degradation. Therefore, the current findings not only explain how ESC-specific miRNAs are preserved and accumulated in iPSCs and ESCs but also demonstrate an important function of glycylglycerins in protecting the structural integrity of highly degradable miRNAs, providing a useful means for maintaining miRNA/siRNA function as well as developing the related RNA interference (RNAi) applications. Oxford University Press 2016-06-02 2016-03-21 /pmc/articles/PMC4889939/ /pubmed/27001514 http://dx.doi.org/10.1093/nar/gkw186 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 RNA
Chang-Lin, Samantha
Hung, Albert
Chang, Donald C.
Lin, Yi-Wen
Ying, Shao-Yao
Lin, Shi-Lung
Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells
title Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells
title_full Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells
title_fullStr Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells
title_full_unstemmed Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells
title_short Novel glycylated sugar alcohols protect ESC-specific microRNAs from degradation in iPS cells
title_sort novel glycylated sugar alcohols protect esc-specific micrornas from degradation in ips cells
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889939/
https://www.ncbi.nlm.nih.gov/pubmed/27001514
http://dx.doi.org/10.1093/nar/gkw186
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