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Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii

Genetic compensation has been proposed to explain phenotypic differences between gene knockouts and knockdowns in several metazoan and plant model systems. With the rapid development of reverse genetic tools such as CRISPR/Cas9 and RNAi in microalgae, it is increasingly important to assess whether g...

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Autores principales: Lee, Yi‐Ying, Park, Rudolph, Miller, Stephen M., Li, Yantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545326/
https://www.ncbi.nlm.nih.gov/pubmed/35727866
http://dx.doi.org/10.1111/tpj.15874
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author Lee, Yi‐Ying
Park, Rudolph
Miller, Stephen M.
Li, Yantao
author_facet Lee, Yi‐Ying
Park, Rudolph
Miller, Stephen M.
Li, Yantao
author_sort Lee, Yi‐Ying
collection PubMed
description Genetic compensation has been proposed to explain phenotypic differences between gene knockouts and knockdowns in several metazoan and plant model systems. With the rapid development of reverse genetic tools such as CRISPR/Cas9 and RNAi in microalgae, it is increasingly important to assess whether genetic compensation affects the phenotype of engineered algal mutants. While exploring triacylglycerol (TAG) biosynthesis pathways in the model alga Chlamydomonas reinhardtii, it was discovered that knockout of certain genes catalyzing rate‐limiting steps of TAG biosynthesis, type‐2 diacylglycerol acyltransferase genes (DGTTs), triggered genetic compensation under abiotic stress conditions. Genetic compensation of a DGTT1 null mutation by a related PDAT gene was observed regardless of the strain background or mutagenesis approach, for example, CRISPR/Cas 9 or insertional mutagenesis. However, no compensation was found in the PDAT knockout mutant. The effect of PDAT knockout was evaluated in a Δvtc1 mutant, in which PDAT was upregulated under stress, resulting in a 90% increase in TAG content. Knockout of PDAT in the Δvtc1 background induced a 12.8‐fold upregulation of DGTT1 and a 272.3% increase in TAG content in Δvtc1/pdat1 cells, while remaining viable. These data suggest that genetic compensation contributes to the genetic robustness of microalgal TAG biosynthetic pathways, maintaining lipid and redox homeostasis in the knockout mutants under abiotic stress. This work demonstrates examples of genetic compensation in microalgae, implies the physiological relevance of genetic compensation in TAG biosynthesis under stress, and provides guidance for future genetic engineering and mutant characterization efforts.
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spelling pubmed-95453262022-10-14 Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii Lee, Yi‐Ying Park, Rudolph Miller, Stephen M. Li, Yantao Plant J Original Articles Genetic compensation has been proposed to explain phenotypic differences between gene knockouts and knockdowns in several metazoan and plant model systems. With the rapid development of reverse genetic tools such as CRISPR/Cas9 and RNAi in microalgae, it is increasingly important to assess whether genetic compensation affects the phenotype of engineered algal mutants. While exploring triacylglycerol (TAG) biosynthesis pathways in the model alga Chlamydomonas reinhardtii, it was discovered that knockout of certain genes catalyzing rate‐limiting steps of TAG biosynthesis, type‐2 diacylglycerol acyltransferase genes (DGTTs), triggered genetic compensation under abiotic stress conditions. Genetic compensation of a DGTT1 null mutation by a related PDAT gene was observed regardless of the strain background or mutagenesis approach, for example, CRISPR/Cas 9 or insertional mutagenesis. However, no compensation was found in the PDAT knockout mutant. The effect of PDAT knockout was evaluated in a Δvtc1 mutant, in which PDAT was upregulated under stress, resulting in a 90% increase in TAG content. Knockout of PDAT in the Δvtc1 background induced a 12.8‐fold upregulation of DGTT1 and a 272.3% increase in TAG content in Δvtc1/pdat1 cells, while remaining viable. These data suggest that genetic compensation contributes to the genetic robustness of microalgal TAG biosynthetic pathways, maintaining lipid and redox homeostasis in the knockout mutants under abiotic stress. This work demonstrates examples of genetic compensation in microalgae, implies the physiological relevance of genetic compensation in TAG biosynthesis under stress, and provides guidance for future genetic engineering and mutant characterization efforts. John Wiley and Sons Inc. 2022-07-06 2022-08 /pmc/articles/PMC9545326/ /pubmed/35727866 http://dx.doi.org/10.1111/tpj.15874 Text en © 2022 The Authors. The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Lee, Yi‐Ying
Park, Rudolph
Miller, Stephen M.
Li, Yantao
Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii
title Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii
title_full Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii
title_fullStr Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii
title_full_unstemmed Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii
title_short Genetic compensation of triacylglycerol biosynthesis in the green microalga Chlamydomonas reinhardtii
title_sort genetic compensation of triacylglycerol biosynthesis in the green microalga chlamydomonas reinhardtii
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545326/
https://www.ncbi.nlm.nih.gov/pubmed/35727866
http://dx.doi.org/10.1111/tpj.15874
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