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Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae
Metabolic engineering has been widely used for production of natural medicinal molecules. However, engineering high-yield platforms is hindered in large part by limited knowledge of complex regulatory machinery of metabolic network. N(6)-Methyladenosine (m(6)A) modification of RNA plays critical rol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326246/ https://www.ncbi.nlm.nih.gov/pubmed/37425036 http://dx.doi.org/10.1016/j.apsb.2023.01.002 |
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author | Zhu, Jianxun An, Tianyue Zha, Wenlong Gao, Ke Li, Ting Zi, Jiachen |
author_facet | Zhu, Jianxun An, Tianyue Zha, Wenlong Gao, Ke Li, Ting Zi, Jiachen |
author_sort | Zhu, Jianxun |
collection | PubMed |
description | Metabolic engineering has been widely used for production of natural medicinal molecules. However, engineering high-yield platforms is hindered in large part by limited knowledge of complex regulatory machinery of metabolic network. N(6)-Methyladenosine (m(6)A) modification of RNA plays critical roles in regulation of gene expression. Herein, we identify 1470 putatively m(6)A peaks within 1151 genes from the haploid Saccharomyces cerevisiae strain. Among them, the transcript levels of 94 genes falling into the pathways which are frequently optimized for chemical production, are remarkably altered upon overexpression of IME4 (the yeast m(6)A methyltransferase). In particular, IME4 overexpression elevates the mRNA levels of the methylated genes in the glycolysis, acetyl-CoA synthesis and shikimate/aromatic amino acid synthesis modules. Furthermore, ACS1 and ADH2, two key genes responsible for acetyl-CoA synthesis, are induced by IME4 overexpression in a transcription factor-mediated manner. Finally, we show IME4 overexpression can significantly increase the titers of isoprenoids and aromatic compounds. Manipulation of m(6)A therefore adds a new layer of metabolic regulatory machinery and may be broadly used in bioproduction of various medicinal molecules of terpenoid and phenol classes. |
format | Online Article Text |
id | pubmed-10326246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103262462023-07-08 Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae Zhu, Jianxun An, Tianyue Zha, Wenlong Gao, Ke Li, Ting Zi, Jiachen Acta Pharm Sin B Original Article Metabolic engineering has been widely used for production of natural medicinal molecules. However, engineering high-yield platforms is hindered in large part by limited knowledge of complex regulatory machinery of metabolic network. N(6)-Methyladenosine (m(6)A) modification of RNA plays critical roles in regulation of gene expression. Herein, we identify 1470 putatively m(6)A peaks within 1151 genes from the haploid Saccharomyces cerevisiae strain. Among them, the transcript levels of 94 genes falling into the pathways which are frequently optimized for chemical production, are remarkably altered upon overexpression of IME4 (the yeast m(6)A methyltransferase). In particular, IME4 overexpression elevates the mRNA levels of the methylated genes in the glycolysis, acetyl-CoA synthesis and shikimate/aromatic amino acid synthesis modules. Furthermore, ACS1 and ADH2, two key genes responsible for acetyl-CoA synthesis, are induced by IME4 overexpression in a transcription factor-mediated manner. Finally, we show IME4 overexpression can significantly increase the titers of isoprenoids and aromatic compounds. Manipulation of m(6)A therefore adds a new layer of metabolic regulatory machinery and may be broadly used in bioproduction of various medicinal molecules of terpenoid and phenol classes. Elsevier 2023-06 2023-01-10 /pmc/articles/PMC10326246/ /pubmed/37425036 http://dx.doi.org/10.1016/j.apsb.2023.01.002 Text en © 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Zhu, Jianxun An, Tianyue Zha, Wenlong Gao, Ke Li, Ting Zi, Jiachen Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae |
title | Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae |
title_full | Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae |
title_fullStr | Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae |
title_full_unstemmed | Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae |
title_short | Manipulation of IME4 expression, a global regulation strategy for metabolic engineering in Saccharomyces cerevisiae |
title_sort | manipulation of ime4 expression, a global regulation strategy for metabolic engineering in saccharomyces cerevisiae |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326246/ https://www.ncbi.nlm.nih.gov/pubmed/37425036 http://dx.doi.org/10.1016/j.apsb.2023.01.002 |
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