Bundle sheath suberization in grass leaves: multiple barriers to characterization
High-yielding, stress-tolerant grass crops are essential to meet future food and energy demands. Efforts are underway to engineer improved varieties of the C 3 cereal crop rice by introducing NADP-malic enzyme C 4 photosynthesis using maize as a model system. However, several modifications to the ri...
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Veröffentlicht in: | Journal of experimental botany 2014-07, Vol.65 (13), p.3371-3380 |
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description | High-yielding, stress-tolerant grass crops are essential to meet future food and energy demands. Efforts are underway to engineer improved varieties of the C 3 cereal crop rice by introducing NADP-malic enzyme C 4 photosynthesis using maize as a model system. However, several modifications to the rice leaf vasculature are potentially necessary, including the introduction of suberin lamellae into the bundle sheath cell walls. Suberized cell walls are ubiquitous in the root endodermis of all grasses, and developmental similarities are apparent between endodermis and bundle sheath cell walls. Nonetheless, there is considerable heterogeneity in sheath cell development and suberin composition both within and between grass taxa. The effect of this variation on physiological function remains ambiguous over forty years after suberin lamellae were initially proposed to regulate solute and photoassimilate fluxes and C 4 gas exchange. Interspecies variation has confounded efforts to ascribe physiological differences specifically to the presence or absence of suberin lamellae. Thus, specific perturbation of suberization within a uniform genetic background is needed, but, until recently, the genetic resources to manipulate suberin composition in the grasses were largely unavailable. The recent dissection of the suberin biosynthesis pathway in model dicots and the identification of several promising candidate genes in model grasses will facilitate the characterization of the first suberin biosynthesis genes in a monocot. Much remains to be learned about the role of bundle sheath suberization in leaf physiology, but the stage is set for significant advances in the near future. |
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Efforts are underway to engineer improved varieties of the C 3 cereal crop rice by introducing NADP-malic enzyme C 4 photosynthesis using maize as a model system. However, several modifications to the rice leaf vasculature are potentially necessary, including the introduction of suberin lamellae into the bundle sheath cell walls. Suberized cell walls are ubiquitous in the root endodermis of all grasses, and developmental similarities are apparent between endodermis and bundle sheath cell walls. Nonetheless, there is considerable heterogeneity in sheath cell development and suberin composition both within and between grass taxa. The effect of this variation on physiological function remains ambiguous over forty years after suberin lamellae were initially proposed to regulate solute and photoassimilate fluxes and C 4 gas exchange. Interspecies variation has confounded efforts to ascribe physiological differences specifically to the presence or absence of suberin lamellae. Thus, specific perturbation of suberization within a uniform genetic background is needed, but, until recently, the genetic resources to manipulate suberin composition in the grasses were largely unavailable. The recent dissection of the suberin biosynthesis pathway in model dicots and the identification of several promising candidate genes in model grasses will facilitate the characterization of the first suberin biosynthesis genes in a monocot. Much remains to be learned about the role of bundle sheath suberization in leaf physiology, but the stage is set for significant advances in the near future.</description><identifier>ISSN: 0022-0957</identifier><identifier>EISSN: 1460-2431</identifier><identifier>DOI: 10.1093/jxb/eru108</identifier><identifier>PMID: 24659485</identifier><language>eng</language><publisher>England: Oxford University Press [etc.]</publisher><subject>Biosynthesis ; Biosynthetic Pathways ; Bundle sheath cells ; carbon dioxide ; Cell Wall - ultrastructure ; Cell walls ; Corn ; Crops, Agricultural ; endodermis ; Fatty acids ; Gene Expression Regulation, Developmental ; Gene Expression Regulation, Plant ; Grasses ; leaves ; Lipids - biosynthesis ; Plant Leaves - growth & development ; Plant Leaves - metabolism ; Plant Leaves - ultrastructure ; Plant physiology ; Plant roots ; Plant Roots - growth & development ; Plant Roots - metabolism ; Plant Roots - ultrastructure ; Plant Vascular Bundle - growth & development ; Plant Vascular Bundle - metabolism ; Plant Vascular Bundle - ultrastructure ; Poaceae - growth & development ; Poaceae - metabolism ; Poaceae - ultrastructure ; REVIEW PAPER ; Rice ; Suberization</subject><ispartof>Journal of experimental botany, 2014-07, Vol.65 (13), p.3371-3380</ispartof><rights>Society for Experimental Biology 2014</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-97a2b748ae5629334c5d5390a588d4112cf07e179cbc0c82281e4414f925dc593</citedby><cites>FETCH-LOGICAL-c435t-97a2b748ae5629334c5d5390a588d4112cf07e179cbc0c82281e4414f925dc593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24044017$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24044017$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24659485$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mertz, Rachel A</creatorcontrib><creatorcontrib>Brutnell, Thomas P</creatorcontrib><title>Bundle sheath suberization in grass leaves: multiple barriers to characterization</title><title>Journal of experimental botany</title><addtitle>J Exp Bot</addtitle><description>High-yielding, stress-tolerant grass crops are essential to meet future food and energy demands. Efforts are underway to engineer improved varieties of the C 3 cereal crop rice by introducing NADP-malic enzyme C 4 photosynthesis using maize as a model system. However, several modifications to the rice leaf vasculature are potentially necessary, including the introduction of suberin lamellae into the bundle sheath cell walls. Suberized cell walls are ubiquitous in the root endodermis of all grasses, and developmental similarities are apparent between endodermis and bundle sheath cell walls. Nonetheless, there is considerable heterogeneity in sheath cell development and suberin composition both within and between grass taxa. The effect of this variation on physiological function remains ambiguous over forty years after suberin lamellae were initially proposed to regulate solute and photoassimilate fluxes and C 4 gas exchange. Interspecies variation has confounded efforts to ascribe physiological differences specifically to the presence or absence of suberin lamellae. Thus, specific perturbation of suberization within a uniform genetic background is needed, but, until recently, the genetic resources to manipulate suberin composition in the grasses were largely unavailable. The recent dissection of the suberin biosynthesis pathway in model dicots and the identification of several promising candidate genes in model grasses will facilitate the characterization of the first suberin biosynthesis genes in a monocot. Much remains to be learned about the role of bundle sheath suberization in leaf physiology, but the stage is set for significant advances in the near future.</description><subject>Biosynthesis</subject><subject>Biosynthetic Pathways</subject><subject>Bundle sheath cells</subject><subject>carbon dioxide</subject><subject>Cell Wall - ultrastructure</subject><subject>Cell walls</subject><subject>Corn</subject><subject>Crops, Agricultural</subject><subject>endodermis</subject><subject>Fatty acids</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gene Expression Regulation, Plant</subject><subject>Grasses</subject><subject>leaves</subject><subject>Lipids - biosynthesis</subject><subject>Plant Leaves - growth & development</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Leaves - ultrastructure</subject><subject>Plant physiology</subject><subject>Plant roots</subject><subject>Plant Roots - growth & development</subject><subject>Plant Roots - metabolism</subject><subject>Plant Roots - ultrastructure</subject><subject>Plant Vascular Bundle - growth & development</subject><subject>Plant Vascular Bundle - metabolism</subject><subject>Plant Vascular Bundle - ultrastructure</subject><subject>Poaceae - growth & development</subject><subject>Poaceae - metabolism</subject><subject>Poaceae - ultrastructure</subject><subject>REVIEW PAPER</subject><subject>Rice</subject><subject>Suberization</subject><issn>0022-0957</issn><issn>1460-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtLxDAUhYMoOo5u3KtdilDnJs1tG3c6-IIBEZ11SNN0pkMfY5KK-uutdBxc3cX5zoH7EXJC4YqCiCarz2xibEch3SEjymMIGY_oLhkBMBaCwOSAHDq3AgAExH1ywHiMgqc4Ii-3XZNXJnBLo_wycF1mbPmtfNk2QdkEC6ucCyqjPoy7Duqu8uW6pzNlbWmsC3wb6KWySvtt7YjsFapy5nhzx2R-f_c2fQxnzw9P05tZqHmEPhSJYlnCU2UwZiKKuMYcIwEK0zTnlDJdQGJoInSmQaeMpdRwTnkhGOYaRTQmF8Pu2rbvnXFe1qXTpqpUY9rOSYrIeQIixh69HFBtW-esKeTalrWyX5KC_FUoe4VyUNjDZ5vdLqtNvkX_nPXA6QCsnG_tvxw4B5r0-fmQF6qVamFLJ-evDCj2_mmC_bM_VPGADA</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Mertz, Rachel A</creator><creator>Brutnell, Thomas P</creator><general>Oxford University Press [etc.]</general><general>Oxford University Press</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140701</creationdate><title>Bundle sheath suberization in grass leaves: multiple barriers to characterization</title><author>Mertz, Rachel A ; Brutnell, Thomas P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-97a2b748ae5629334c5d5390a588d4112cf07e179cbc0c82281e4414f925dc593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biosynthesis</topic><topic>Biosynthetic Pathways</topic><topic>Bundle sheath cells</topic><topic>carbon dioxide</topic><topic>Cell Wall - ultrastructure</topic><topic>Cell walls</topic><topic>Corn</topic><topic>Crops, Agricultural</topic><topic>endodermis</topic><topic>Fatty acids</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Gene Expression Regulation, Plant</topic><topic>Grasses</topic><topic>leaves</topic><topic>Lipids - biosynthesis</topic><topic>Plant Leaves - growth & development</topic><topic>Plant Leaves - metabolism</topic><topic>Plant Leaves - ultrastructure</topic><topic>Plant physiology</topic><topic>Plant roots</topic><topic>Plant Roots - growth & development</topic><topic>Plant Roots - metabolism</topic><topic>Plant Roots - ultrastructure</topic><topic>Plant Vascular Bundle - growth & development</topic><topic>Plant Vascular Bundle - metabolism</topic><topic>Plant Vascular Bundle - ultrastructure</topic><topic>Poaceae - growth & development</topic><topic>Poaceae - metabolism</topic><topic>Poaceae - ultrastructure</topic><topic>REVIEW PAPER</topic><topic>Rice</topic><topic>Suberization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mertz, Rachel A</creatorcontrib><creatorcontrib>Brutnell, Thomas P</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of experimental botany</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mertz, Rachel A</au><au>Brutnell, Thomas P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bundle sheath suberization in grass leaves: multiple barriers to characterization</atitle><jtitle>Journal of experimental botany</jtitle><addtitle>J Exp Bot</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>65</volume><issue>13</issue><spage>3371</spage><epage>3380</epage><pages>3371-3380</pages><issn>0022-0957</issn><eissn>1460-2431</eissn><abstract>High-yielding, stress-tolerant grass crops are essential to meet future food and energy demands. Efforts are underway to engineer improved varieties of the C 3 cereal crop rice by introducing NADP-malic enzyme C 4 photosynthesis using maize as a model system. However, several modifications to the rice leaf vasculature are potentially necessary, including the introduction of suberin lamellae into the bundle sheath cell walls. Suberized cell walls are ubiquitous in the root endodermis of all grasses, and developmental similarities are apparent between endodermis and bundle sheath cell walls. Nonetheless, there is considerable heterogeneity in sheath cell development and suberin composition both within and between grass taxa. The effect of this variation on physiological function remains ambiguous over forty years after suberin lamellae were initially proposed to regulate solute and photoassimilate fluxes and C 4 gas exchange. Interspecies variation has confounded efforts to ascribe physiological differences specifically to the presence or absence of suberin lamellae. Thus, specific perturbation of suberization within a uniform genetic background is needed, but, until recently, the genetic resources to manipulate suberin composition in the grasses were largely unavailable. The recent dissection of the suberin biosynthesis pathway in model dicots and the identification of several promising candidate genes in model grasses will facilitate the characterization of the first suberin biosynthesis genes in a monocot. Much remains to be learned about the role of bundle sheath suberization in leaf physiology, but the stage is set for significant advances in the near future.</abstract><cop>England</cop><pub>Oxford University Press [etc.]</pub><pmid>24659485</pmid><doi>10.1093/jxb/eru108</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biosynthesis Biosynthetic Pathways Bundle sheath cells carbon dioxide Cell Wall - ultrastructure Cell walls Corn Crops, Agricultural endodermis Fatty acids Gene Expression Regulation, Developmental Gene Expression Regulation, Plant Grasses leaves Lipids - biosynthesis Plant Leaves - growth & development Plant Leaves - metabolism Plant Leaves - ultrastructure Plant physiology Plant roots Plant Roots - growth & development Plant Roots - metabolism Plant Roots - ultrastructure Plant Vascular Bundle - growth & development Plant Vascular Bundle - metabolism Plant Vascular Bundle - ultrastructure Poaceae - growth & development Poaceae - metabolism Poaceae - ultrastructure REVIEW PAPER Rice Suberization |
title | Bundle sheath suberization in grass leaves: multiple barriers to characterization |
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