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Methylglyoxal: An Emerging Signaling Molecule in Plant Abiotic Stress Responses and Tolerance

Identifieur interne : 001381 ( Pmc/Curation ); précédent : 001380; suivant : 001382

Methylglyoxal: An Emerging Signaling Molecule in Plant Abiotic Stress Responses and Tolerance

Auteurs : Tahsina S. Hoque [Bangladesh] ; Mohammad A. Hossain [Bangladesh] ; Mohammad G. Mostofa [Bangladesh] ; David J. Burritt [Nouvelle-Zélande] ; Masayuki Fujita [Japon] ; Lam-Son P. Tran [Viêt Nam, Japon]

Source :

RBID : PMC:5020096

Abstract

The oxygenated short aldehyde methylglyoxal (MG) is produced in plants as a by-product of a number of metabolic reactions, including elimination of phosphate groups from glycolysis intermediates dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. MG is mostly detoxified by the combined actions of the enzymes glyoxalase I and glyoxalase II that together with glutathione make up the glyoxalase system. Under normal growth conditions, basal levels of MG remain low in plants; however, when plants are exposed to abiotic stress, MG can accumulate to much higher levels. Stress-induced MG functions as a toxic molecule, inhibiting different developmental processes, including seed germination, photosynthesis and root growth, whereas MG, at low levels, acts as an important signaling molecule, involved in regulating diverse events, such as cell proliferation and survival, control of the redox status of cells, and many other aspects of general metabolism and cellular homeostases. MG can modulate plant stress responses by regulating stomatal opening and closure, the production of reactive oxygen species, cytosolic calcium ion concentrations, the activation of inward rectifying potassium channels and the expression of many stress-responsive genes. MG appears to play important roles in signal transduction by transmitting and amplifying cellular signals and functions that promote adaptation of plants growing under adverse environmental conditions. Thus, MG is now considered as a potential biochemical marker for plant abiotic stress tolerance, and is receiving considerable attention by the scientific community. In this review, we will summarize recent findings regarding MG metabolism in plants under abiotic stress, and evaluate the concept of MG signaling. In addition, we will demonstrate the importance of giving consideration to MG metabolism and the glyoxalase system, when investigating plant adaptation and responses to various environmental stresses.


Url:
DOI: 10.3389/fpls.2016.01341
PubMed: 27679640
PubMed Central: 5020096

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PMC:5020096

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<p>The oxygenated short aldehyde methylglyoxal (MG) is produced in plants as a by-product of a number of metabolic reactions, including elimination of phosphate groups from glycolysis intermediates dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. MG is mostly detoxified by the combined actions of the enzymes glyoxalase I and glyoxalase II that together with glutathione make up the glyoxalase system. Under normal growth conditions, basal levels of MG remain low in plants; however, when plants are exposed to abiotic stress, MG can accumulate to much higher levels. Stress-induced MG functions as a toxic molecule, inhibiting different developmental processes, including seed germination, photosynthesis and root growth, whereas MG, at low levels, acts as an important signaling molecule, involved in regulating diverse events, such as cell proliferation and survival, control of the redox status of cells, and many other aspects of general metabolism and cellular homeostases. MG can modulate plant stress responses by regulating stomatal opening and closure, the production of reactive oxygen species, cytosolic calcium ion concentrations, the activation of inward rectifying potassium channels and the expression of many stress-responsive genes. MG appears to play important roles in signal transduction by transmitting and amplifying cellular signals and functions that promote adaptation of plants growing under adverse environmental conditions. Thus, MG is now considered as a potential biochemical marker for plant abiotic stress tolerance, and is receiving considerable attention by the scientific community. In this review, we will summarize recent findings regarding MG metabolism in plants under abiotic stress, and evaluate the concept of MG signaling. In addition, we will demonstrate the importance of giving consideration to MG metabolism and the glyoxalase system, when investigating plant adaptation and responses to various environmental stresses.</p>
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</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Front Plant Sci</journal-id>
<journal-id journal-id-type="iso-abbrev">Front Plant Sci</journal-id>
<journal-id journal-id-type="publisher-id">Front. Plant Sci.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Plant Science</journal-title>
</journal-title-group>
<issn pub-type="epub">1664-462X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">27679640</article-id>
<article-id pub-id-type="pmc">5020096</article-id>
<article-id pub-id-type="doi">10.3389/fpls.2016.01341</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Plant Science</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Methylglyoxal: An Emerging Signaling Molecule in Plant Abiotic Stress Responses and Tolerance</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Hoque</surname>
<given-names>Tahsina S.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/373573/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hossain</surname>
<given-names>Mohammad A.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/191808/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mostofa</surname>
<given-names>Mohammad G.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/241745/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Burritt</surname>
<given-names>David J.</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/220674/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fujita</surname>
<given-names>Masayuki</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/191807/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tran</surname>
<given-names>Lam-Son P.</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<xref ref-type="aff" rid="aff7">
<sup>7</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/64534/overview"></uri>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Soil Science, Bangladesh Agricultural University</institution>
<country>Mymensingh, Bangladesh</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Department of Genetics and Plant Breeding, Bangladesh Agricultural University</institution>
<country>Mymensingh, Bangladesh</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Biochemistry and Molecular Biology, Bangabandhu Sheikh Mujibur Rahman Agricultural University</institution>
<country>Gazipur, Bangladesh</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Botany, University of Otago</institution>
<country>Dunedin, New Zealand</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Laboratory of Plant Stress Responses, Department of Applied Biological Science, Faculty of Agriculture, Kagawa University</institution>
<country>Kagawa, Japan</country>
</aff>
<aff id="aff6">
<sup>6</sup>
<institution>Plant Abiotic Stress Research Group & Faculty of Applied Sciences, Ton Duc Thang University</institution>
<country>Ho Chi Minh City, Vietnam</country>
</aff>
<aff id="aff7">
<sup>7</sup>
<institution>Signaling Pathway Research Unit, RIKEN Center for Sustainable Resource Science</institution>
<country>Yokohama, Japan</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by:
<italic>Susana Araújo, Universidade Nova de Lisboa, Portugal</italic>
</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by:
<italic>Veronica Graciela Maurino, Heinrich Heine University Düsseldorf, Germany; Abu Hena Mostafa Kamal, University of Texas at Arlington, USA</italic>
</p>
</fn>
<corresp id="fn001">*Correspondence:
<italic>Mohammad G. Mostofa,
<email xlink:type="simple">mostofa@bsmrau.edu.bd</email>
Lam-Son P. Tran,
<email xlink:type="simple">sontran@tdt.edu.vn</email>
;
<email xlink:type="simple">son.tran@riken.jp</email>
</italic>
</corresp>
<fn fn-type="other" id="fn002">
<p>This article was submitted to Crop Science and Horticulture, a section of the journal Frontiers in Plant Science</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>13</day>
<month>9</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="collection">
<year>2016</year>
</pub-date>
<volume>7</volume>
<elocation-id>1341</elocation-id>
<history>
<date date-type="received">
<day>14</day>
<month>6</month>
<year>2016</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>8</month>
<year>2016</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2016 Hoque, Hossain, Mostofa, Burritt, Fujita and Tran.</copyright-statement>
<copyright-year>2016</copyright-year>
<copyright-holder>Hoque, Hossain, Mostofa, Burritt, Fujita and Tran</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>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.</license-p>
</license>
</permissions>
<abstract>
<p>The oxygenated short aldehyde methylglyoxal (MG) is produced in plants as a by-product of a number of metabolic reactions, including elimination of phosphate groups from glycolysis intermediates dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. MG is mostly detoxified by the combined actions of the enzymes glyoxalase I and glyoxalase II that together with glutathione make up the glyoxalase system. Under normal growth conditions, basal levels of MG remain low in plants; however, when plants are exposed to abiotic stress, MG can accumulate to much higher levels. Stress-induced MG functions as a toxic molecule, inhibiting different developmental processes, including seed germination, photosynthesis and root growth, whereas MG, at low levels, acts as an important signaling molecule, involved in regulating diverse events, such as cell proliferation and survival, control of the redox status of cells, and many other aspects of general metabolism and cellular homeostases. MG can modulate plant stress responses by regulating stomatal opening and closure, the production of reactive oxygen species, cytosolic calcium ion concentrations, the activation of inward rectifying potassium channels and the expression of many stress-responsive genes. MG appears to play important roles in signal transduction by transmitting and amplifying cellular signals and functions that promote adaptation of plants growing under adverse environmental conditions. Thus, MG is now considered as a potential biochemical marker for plant abiotic stress tolerance, and is receiving considerable attention by the scientific community. In this review, we will summarize recent findings regarding MG metabolism in plants under abiotic stress, and evaluate the concept of MG signaling. In addition, we will demonstrate the importance of giving consideration to MG metabolism and the glyoxalase system, when investigating plant adaptation and responses to various environmental stresses.</p>
</abstract>
<kwd-group>
<kwd>abiotic stress</kwd>
<kwd>glyoxalases</kwd>
<kwd>methylglyoxal</kwd>
<kwd>reactive oxygen species</kwd>
<kwd>signaling crosstalk</kwd>
<kwd>stress tolerance mechanism</kwd>
</kwd-group>
<counts>
<fig-count count="2"></fig-count>
<table-count count="2"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="120"></ref-count>
<page-count count="11"></page-count>
<word-count count="0"></word-count>
</counts>
</article-meta>
</front>
</pmc>
</record>

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