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Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein
OBJECTIVES: We used miRNA and proteomic profiling to understand intracellular pathways that contribute to high and low specific productivity (Qp) phenotypes in CHO clonally derived cell lines (CDCLs) from the same cell line generation project. RESULTS: Differentially expressed (DE) miRNAs were ident...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254715/ https://www.ncbi.nlm.nih.gov/pubmed/34131805 http://dx.doi.org/10.1007/s10529-021-03153-7 |
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author | Bryan, Laura Henry, Michael Barron, Niall Gallagher, Clair Kelly, Ronan M. Frye, Christopher C. Osborne, Matthew D. Clynes, Martin Meleady, Paula |
author_facet | Bryan, Laura Henry, Michael Barron, Niall Gallagher, Clair Kelly, Ronan M. Frye, Christopher C. Osborne, Matthew D. Clynes, Martin Meleady, Paula |
author_sort | Bryan, Laura |
collection | PubMed |
description | OBJECTIVES: We used miRNA and proteomic profiling to understand intracellular pathways that contribute to high and low specific productivity (Qp) phenotypes in CHO clonally derived cell lines (CDCLs) from the same cell line generation project. RESULTS: Differentially expressed (DE) miRNAs were identified which are predicted to target several proteins associated with protein folding. MiR-200a was found to have a number of predicted targets associated with the unfolded protein response (UPR) which were shown to have decreased expression in high Qp CDCLs and have no detected change at the mRNA level. MiR-200a overexpression in a CHO CDCL was found to increase recombinant protein titer by 1.2 fold and Qp by 1.8 fold. CONCLUSION: These results may suggest a role for miR-200a in post-transcriptional regulation of the UPR, presenting miR-200a as a potential target for engineering industrially attractive CHO cell phenotypes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10529-021-03153-7. |
format | Online Article Text |
id | pubmed-8254715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-82547152021-07-20 Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein Bryan, Laura Henry, Michael Barron, Niall Gallagher, Clair Kelly, Ronan M. Frye, Christopher C. Osborne, Matthew D. Clynes, Martin Meleady, Paula Biotechnol Lett Original Research Paper OBJECTIVES: We used miRNA and proteomic profiling to understand intracellular pathways that contribute to high and low specific productivity (Qp) phenotypes in CHO clonally derived cell lines (CDCLs) from the same cell line generation project. RESULTS: Differentially expressed (DE) miRNAs were identified which are predicted to target several proteins associated with protein folding. MiR-200a was found to have a number of predicted targets associated with the unfolded protein response (UPR) which were shown to have decreased expression in high Qp CDCLs and have no detected change at the mRNA level. MiR-200a overexpression in a CHO CDCL was found to increase recombinant protein titer by 1.2 fold and Qp by 1.8 fold. CONCLUSION: These results may suggest a role for miR-200a in post-transcriptional regulation of the UPR, presenting miR-200a as a potential target for engineering industrially attractive CHO cell phenotypes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10529-021-03153-7. Springer Netherlands 2021-06-16 2021 /pmc/articles/PMC8254715/ /pubmed/34131805 http://dx.doi.org/10.1007/s10529-021-03153-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Research Paper Bryan, Laura Henry, Michael Barron, Niall Gallagher, Clair Kelly, Ronan M. Frye, Christopher C. Osborne, Matthew D. Clynes, Martin Meleady, Paula Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein |
title | Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein |
title_full | Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein |
title_fullStr | Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein |
title_full_unstemmed | Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein |
title_short | Differential expression of miRNAs and functional role of mir-200a in high and low productivity CHO cells expressing an Fc fusion protein |
title_sort | differential expression of mirnas and functional role of mir-200a in high and low productivity cho cells expressing an fc fusion protein |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254715/ https://www.ncbi.nlm.nih.gov/pubmed/34131805 http://dx.doi.org/10.1007/s10529-021-03153-7 |
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