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Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues

Diacylglycerol acyltransferases (DGAT) catalyze the final and rate-limiting step of triacylglycerol (TAG) biosynthesis in eukaryotic organisms. DGAT genes have been identified in numerous organisms. Multiple isoforms of DGAT are present in eukaryotes. We previously cloned DGAT1 and DGAT2 genes of tu...

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Autores principales: Cao, Heping, Shockey, Jay M., Klasson, K. Thomas, Chapital, Dorselyn C., Mason, Catherine B., Scheffler, Brian E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795650/
https://www.ncbi.nlm.nih.gov/pubmed/24146944
http://dx.doi.org/10.1371/journal.pone.0076946
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author Cao, Heping
Shockey, Jay M.
Klasson, K. Thomas
Chapital, Dorselyn C.
Mason, Catherine B.
Scheffler, Brian E.
author_facet Cao, Heping
Shockey, Jay M.
Klasson, K. Thomas
Chapital, Dorselyn C.
Mason, Catherine B.
Scheffler, Brian E.
author_sort Cao, Heping
collection PubMed
description Diacylglycerol acyltransferases (DGAT) catalyze the final and rate-limiting step of triacylglycerol (TAG) biosynthesis in eukaryotic organisms. DGAT genes have been identified in numerous organisms. Multiple isoforms of DGAT are present in eukaryotes. We previously cloned DGAT1 and DGAT2 genes of tung tree (Vernicia fordii), whose novel seed TAGs are useful in a wide range of industrial applications. The objective of this study was to understand the developmental regulation of DGAT family gene expression in tung tree. To this end, we first cloned a tung tree gene encoding DGAT3, a putatively soluble form of DGAT that possesses 11 completely conserved amino acid residues shared among 27 DGAT3s from 19 plant species. Unlike DGAT1 and DGAT2 subfamilies, DGAT3 is absent from animals. We then used TaqMan and SYBR Green quantitative real-time PCR, along with northern and western blotting, to study the expression patterns of the three DGAT genes in tung tree tissues. Expression results demonstrate that 1) all three isoforms of DGAT genes are expressed in developing seeds, leaves and flowers; 2) DGAT2 is the major DGAT mRNA in tung seeds, whose expression profile is well-coordinated with the oil profile in developing tung seeds; and 3) DGAT3 is the major form of DGAT mRNA in tung leaves, flowers and immature seeds prior to active tung oil biosynthesis. These results suggest that DGAT2 is probably the major TAG biosynthetic isoform in tung seeds and that DGAT3 gene likely plays a significant role in TAG metabolism in other tissues. Therefore, DGAT2 should be a primary target for tung oil engineering in transgenic organisms.
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spelling pubmed-37956502013-10-21 Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues Cao, Heping Shockey, Jay M. Klasson, K. Thomas Chapital, Dorselyn C. Mason, Catherine B. Scheffler, Brian E. PLoS One Research Article Diacylglycerol acyltransferases (DGAT) catalyze the final and rate-limiting step of triacylglycerol (TAG) biosynthesis in eukaryotic organisms. DGAT genes have been identified in numerous organisms. Multiple isoforms of DGAT are present in eukaryotes. We previously cloned DGAT1 and DGAT2 genes of tung tree (Vernicia fordii), whose novel seed TAGs are useful in a wide range of industrial applications. The objective of this study was to understand the developmental regulation of DGAT family gene expression in tung tree. To this end, we first cloned a tung tree gene encoding DGAT3, a putatively soluble form of DGAT that possesses 11 completely conserved amino acid residues shared among 27 DGAT3s from 19 plant species. Unlike DGAT1 and DGAT2 subfamilies, DGAT3 is absent from animals. We then used TaqMan and SYBR Green quantitative real-time PCR, along with northern and western blotting, to study the expression patterns of the three DGAT genes in tung tree tissues. Expression results demonstrate that 1) all three isoforms of DGAT genes are expressed in developing seeds, leaves and flowers; 2) DGAT2 is the major DGAT mRNA in tung seeds, whose expression profile is well-coordinated with the oil profile in developing tung seeds; and 3) DGAT3 is the major form of DGAT mRNA in tung leaves, flowers and immature seeds prior to active tung oil biosynthesis. These results suggest that DGAT2 is probably the major TAG biosynthetic isoform in tung seeds and that DGAT3 gene likely plays a significant role in TAG metabolism in other tissues. Therefore, DGAT2 should be a primary target for tung oil engineering in transgenic organisms. Public Library of Science 2013-10-11 /pmc/articles/PMC3795650/ /pubmed/24146944 http://dx.doi.org/10.1371/journal.pone.0076946 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Cao, Heping
Shockey, Jay M.
Klasson, K. Thomas
Chapital, Dorselyn C.
Mason, Catherine B.
Scheffler, Brian E.
Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues
title Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues
title_full Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues
title_fullStr Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues
title_full_unstemmed Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues
title_short Developmental Regulation of Diacylglycerol Acyltransferase Family Gene Expression in Tung Tree Tissues
title_sort developmental regulation of diacylglycerol acyltransferase family gene expression in tung tree tissues
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795650/
https://www.ncbi.nlm.nih.gov/pubmed/24146944
http://dx.doi.org/10.1371/journal.pone.0076946
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