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The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping

Enhancer trap systems have been demonstrated to increase the effectiveness of gene identification in rice. In this study, a chlorophyll-deficient mutant, named oscdm1, was screened and characterized in detail from a T-DNA enhancer-tagged population. The oscdm1 plants were different from other chloro...

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Autores principales: Wu, Jinxia, Zhang, Zhiguo, Zhang, Qian, Han, Xiao, Gu, Xiaofeng, Lu, Tiegang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490251/
https://www.ncbi.nlm.nih.gov/pubmed/26191072
http://dx.doi.org/10.3389/fgene.2015.00226
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author Wu, Jinxia
Zhang, Zhiguo
Zhang, Qian
Han, Xiao
Gu, Xiaofeng
Lu, Tiegang
author_facet Wu, Jinxia
Zhang, Zhiguo
Zhang, Qian
Han, Xiao
Gu, Xiaofeng
Lu, Tiegang
author_sort Wu, Jinxia
collection PubMed
description Enhancer trap systems have been demonstrated to increase the effectiveness of gene identification in rice. In this study, a chlorophyll-deficient mutant, named oscdm1, was screened and characterized in detail from a T-DNA enhancer-tagged population. The oscdm1 plants were different from other chlorophyll-deficient mutants; they produced chlorotic leaves at the third leaf stage, which gradually died with further growth of the plants. However, the oscdm1 plants were able to survive exposure to elevated CO(2) levels, similar to photorespiratory mutants. An analysis of the T-DNA flanking sequence in the oscdm1 plants showed that the T-DNA was inserted into the promoter region of a serine hydroxymethyltransferase (SHMT) gene. OsSHMT1 is a key enzyme that is ubiquitous in nature and structurally conserved across kingdoms. The enzyme is responsible for the interconversion of serine and glycine and is essential for cellular one-carbon metabolism. Full-length OsSHMT1 complemented the oscdm1 phenotype, and the downregulation of OsSHMT1 in wild-type plants by RNA interference (RNAi) produced plants that mimicked the oscdm1 phenotype. GUS assays and quantitative PCR revealed the preferential expression of OsSHMT1 in young leaves. TEM revealed serious damage to the thylakoid membrane in oscdm1 chloroplasts. The oscdm1 plants showed more extensive damage than wild type using an IMAGING-PAM fluorometer, especially under high light intensities. OsSHMT1-GFP localized exclusively to mitochondria. Further analysis revealed that the H(2)O(2) content in the oscdm1 plants was twice that in wild type at the fourth leaf stage. This suggests that the thylakoid membrane damage observed in the oscdm1 plants was caused by excessive H(2)O(2). Interestingly, OsSHMT1-overexpressing plants exhibited increased photosynthetic efficiency and improved plant productivity. These results lay the foundation for further study of the OsSHMT1 gene and will help illuminate the functional role of OsSHMT1 in photorespiration in rice.
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spelling pubmed-44902512015-07-17 The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping Wu, Jinxia Zhang, Zhiguo Zhang, Qian Han, Xiao Gu, Xiaofeng Lu, Tiegang Front Genet Plant Science Enhancer trap systems have been demonstrated to increase the effectiveness of gene identification in rice. In this study, a chlorophyll-deficient mutant, named oscdm1, was screened and characterized in detail from a T-DNA enhancer-tagged population. The oscdm1 plants were different from other chlorophyll-deficient mutants; they produced chlorotic leaves at the third leaf stage, which gradually died with further growth of the plants. However, the oscdm1 plants were able to survive exposure to elevated CO(2) levels, similar to photorespiratory mutants. An analysis of the T-DNA flanking sequence in the oscdm1 plants showed that the T-DNA was inserted into the promoter region of a serine hydroxymethyltransferase (SHMT) gene. OsSHMT1 is a key enzyme that is ubiquitous in nature and structurally conserved across kingdoms. The enzyme is responsible for the interconversion of serine and glycine and is essential for cellular one-carbon metabolism. Full-length OsSHMT1 complemented the oscdm1 phenotype, and the downregulation of OsSHMT1 in wild-type plants by RNA interference (RNAi) produced plants that mimicked the oscdm1 phenotype. GUS assays and quantitative PCR revealed the preferential expression of OsSHMT1 in young leaves. TEM revealed serious damage to the thylakoid membrane in oscdm1 chloroplasts. The oscdm1 plants showed more extensive damage than wild type using an IMAGING-PAM fluorometer, especially under high light intensities. OsSHMT1-GFP localized exclusively to mitochondria. Further analysis revealed that the H(2)O(2) content in the oscdm1 plants was twice that in wild type at the fourth leaf stage. This suggests that the thylakoid membrane damage observed in the oscdm1 plants was caused by excessive H(2)O(2). Interestingly, OsSHMT1-overexpressing plants exhibited increased photosynthetic efficiency and improved plant productivity. These results lay the foundation for further study of the OsSHMT1 gene and will help illuminate the functional role of OsSHMT1 in photorespiration in rice. Frontiers Media S.A. 2015-07-03 /pmc/articles/PMC4490251/ /pubmed/26191072 http://dx.doi.org/10.3389/fgene.2015.00226 Text en Copyright © 2015 Wu, Zhang, Zhang, Han, Gu and Lu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Wu, Jinxia
Zhang, Zhiguo
Zhang, Qian
Han, Xiao
Gu, Xiaofeng
Lu, Tiegang
The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
title The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
title_full The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
title_fullStr The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
title_full_unstemmed The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
title_short The molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
title_sort molecular cloning and clarification of a photorespiratory mutant, oscdm1, using enhancer trapping
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490251/
https://www.ncbi.nlm.nih.gov/pubmed/26191072
http://dx.doi.org/10.3389/fgene.2015.00226
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