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subtilisin-like serine protease essential for mucilage release from Arabidopsis seed coats
During Arabidopsis seed development large quantities of mucilage, composed of pectins, are deposited into the apoplast underneath the outer wall of the seed coat. Upon imbibition of mature seeds, the stored mucilage expands through hydration and breaks the outer cell wall that encapsulates the whole...
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Published in: | The Plant journal : for cell and molecular biology 2008-05, Vol.54 (3), p.466-480 |
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creator | Rautengarten, Carsten Usadel, Björn Neumetzler, Lutz Hartmann, Jürgen Büssis, Dirk Altmann, Thomas |
description | During Arabidopsis seed development large quantities of mucilage, composed of pectins, are deposited into the apoplast underneath the outer wall of the seed coat. Upon imbibition of mature seeds, the stored mucilage expands through hydration and breaks the outer cell wall that encapsulates the whole seed. Mutant seeds carrying loss-of-function alleles of AtSBT1.7 that encodes one of 56 Arabidopsis thaliana subtilisin-like serine proteases (subtilases) do not release mucilage upon hydration. Microscopic analysis of the mutant seed coat revealed no visible structural differences compared with wild-type seeds. Weakening of the outer primary wall using cation chelators triggered mucilage release from the seed coats of mutants. However, in contrast to mature wild-type seeds, the mutant's outer cell walls did not rupture at the radial walls of the seed coat epidermal cells, but instead opened at the chalazal end of the seed, and were released in one piece. In atsbt1.7, the total rhamnose and galacturonic acid contents, representing the backbone of mucilage, remained unchanged compared with wild-type seeds. Thus, extrusion and solubility, but not the initial deposition of mucilage, are affected in atsbt1.7 mutants. AtSBT1.7 is localized in the developing seed coat, indicating a role in testa development or maturation. The altered mode of rupture of the outer seed coat wall and mucilage release indicate that AtSBT1.7 triggers the accumulation, and/or activation, of cell wall modifying enzymes necessary either for the loosening of the outer primary cell wall, or to facilitate swelling of the mucilage, as indicated by elevated pectin methylesterase activity in developing atsbt1.7 mutant seeds. |
doi_str_mv | 10.1111/j.1365-313X.2008.03437.x |
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Upon imbibition of mature seeds, the stored mucilage expands through hydration and breaks the outer cell wall that encapsulates the whole seed. Mutant seeds carrying loss-of-function alleles of AtSBT1.7 that encodes one of 56 Arabidopsis thaliana subtilisin-like serine proteases (subtilases) do not release mucilage upon hydration. Microscopic analysis of the mutant seed coat revealed no visible structural differences compared with wild-type seeds. Weakening of the outer primary wall using cation chelators triggered mucilage release from the seed coats of mutants. However, in contrast to mature wild-type seeds, the mutant's outer cell walls did not rupture at the radial walls of the seed coat epidermal cells, but instead opened at the chalazal end of the seed, and were released in one piece. In atsbt1.7, the total rhamnose and galacturonic acid contents, representing the backbone of mucilage, remained unchanged compared with wild-type seeds. Thus, extrusion and solubility, but not the initial deposition of mucilage, are affected in atsbt1.7 mutants. AtSBT1.7 is localized in the developing seed coat, indicating a role in testa development or maturation. The altered mode of rupture of the outer seed coat wall and mucilage release indicate that AtSBT1.7 triggers the accumulation, and/or activation, of cell wall modifying enzymes necessary either for the loosening of the outer primary cell wall, or to facilitate swelling of the mucilage, as indicated by elevated pectin methylesterase activity in developing atsbt1.7 mutant seeds.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/j.1365-313X.2008.03437.x</identifier><identifier>PMID: 18266922</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Adhesives - metabolism ; Arabidopsis - genetics ; Arabidopsis - growth & development ; Arabidopsis - metabolism ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Biological and medical sciences ; Botany ; Carboxylic Ester Hydrolases - genetics ; Carboxylic Ester Hydrolases - metabolism ; cell wall ; Cellular biology ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Plant ; Germination and dormancy ; Hexuronic Acids - metabolism ; mucilage ; Mutation ; pectin methylesterase ; pectinesterase ; Plant physiology and development ; Plants, Genetically Modified ; Reverse Transcriptase Polymerase Chain Reaction ; Rhamnose - metabolism ; seed coat ; Seeds ; Seeds - genetics ; Seeds - growth & development ; Seeds - metabolism ; Serine Endopeptidases - genetics ; Serine Endopeptidases - metabolism ; subtilase ; Subtilisin - genetics ; Subtilisin - metabolism ; testa</subject><ispartof>The Plant journal : for cell and molecular biology, 2008-05, Vol.54 (3), p.466-480</ispartof><rights>2008 University of Potsdam Journal compilation © 2008 Blackwell Publishing Ltd</rights><rights>2008 INIST-CNRS</rights><rights>Journal compilation © 2008 Blackwell Publishing Ltd and the Society for Experimental Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5697-421d38a3fb0bb036b2e45735c9eeb0722150155e8d40f8af273fcc4f0b35800e3</citedby><cites>FETCH-LOGICAL-c5697-421d38a3fb0bb036b2e45735c9eeb0722150155e8d40f8af273fcc4f0b35800e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20317890$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18266922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rautengarten, Carsten</creatorcontrib><creatorcontrib>Usadel, Björn</creatorcontrib><creatorcontrib>Neumetzler, Lutz</creatorcontrib><creatorcontrib>Hartmann, Jürgen</creatorcontrib><creatorcontrib>Büssis, Dirk</creatorcontrib><creatorcontrib>Altmann, Thomas</creatorcontrib><title>subtilisin-like serine protease essential for mucilage release from Arabidopsis seed coats</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>During Arabidopsis seed development large quantities of mucilage, composed of pectins, are deposited into the apoplast underneath the outer wall of the seed coat. Upon imbibition of mature seeds, the stored mucilage expands through hydration and breaks the outer cell wall that encapsulates the whole seed. Mutant seeds carrying loss-of-function alleles of AtSBT1.7 that encodes one of 56 Arabidopsis thaliana subtilisin-like serine proteases (subtilases) do not release mucilage upon hydration. Microscopic analysis of the mutant seed coat revealed no visible structural differences compared with wild-type seeds. Weakening of the outer primary wall using cation chelators triggered mucilage release from the seed coats of mutants. However, in contrast to mature wild-type seeds, the mutant's outer cell walls did not rupture at the radial walls of the seed coat epidermal cells, but instead opened at the chalazal end of the seed, and were released in one piece. In atsbt1.7, the total rhamnose and galacturonic acid contents, representing the backbone of mucilage, remained unchanged compared with wild-type seeds. Thus, extrusion and solubility, but not the initial deposition of mucilage, are affected in atsbt1.7 mutants. AtSBT1.7 is localized in the developing seed coat, indicating a role in testa development or maturation. The altered mode of rupture of the outer seed coat wall and mucilage release indicate that AtSBT1.7 triggers the accumulation, and/or activation, of cell wall modifying enzymes necessary either for the loosening of the outer primary cell wall, or to facilitate swelling of the mucilage, as indicated by elevated pectin methylesterase activity in developing atsbt1.7 mutant seeds.</description><subject>Adhesives - metabolism</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - growth & development</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Biological and medical sciences</subject><subject>Botany</subject><subject>Carboxylic Ester Hydrolases - genetics</subject><subject>Carboxylic Ester Hydrolases - metabolism</subject><subject>cell wall</subject><subject>Cellular biology</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Plant</subject><subject>Germination and dormancy</subject><subject>Hexuronic Acids - metabolism</subject><subject>mucilage</subject><subject>Mutation</subject><subject>pectin methylesterase</subject><subject>pectinesterase</subject><subject>Plant physiology and development</subject><subject>Plants, Genetically Modified</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Rhamnose - metabolism</subject><subject>seed coat</subject><subject>Seeds</subject><subject>Seeds - genetics</subject><subject>Seeds - growth & development</subject><subject>Seeds - metabolism</subject><subject>Serine Endopeptidases - genetics</subject><subject>Serine Endopeptidases - metabolism</subject><subject>subtilase</subject><subject>Subtilisin - genetics</subject><subject>Subtilisin - metabolism</subject><subject>testa</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkEtv1TAQhS0EopfCX4AICXYJYzsPZ8GiqspLlYpEKyE2luOMK1-c5OJJ1Pbf4_ReFYlVZ-OR5jszx4exjEPBU33YFlzWVS65_FkIAFWALGVT3D5hm4fBU7aBtoa8Kbk4Yi-ItgC8kXX5nB1xJeq6FWLDftHSzT548mMe_G_MCKMfMdvFaUZDmCERjrM3IXNTzIbF-mCuMYsY7scuTkN2Ek3n-2lHnpIe-8xOZqaX7JkzgfDV4T1mV5_OLk-_5OcXn7-enpzntqrbJi8F76Uy0nXQdSDrTmBZNbKyLWIHjRC8Al5VqPoSnDJONNJZWzroZKUAUB6z9_u9yfOfBWnWgyeLIZgRp4V03XKpeA0JfPsfuJ2WOCZvWnBZcdkCT5DaQzZORBGd3kU_mHinOeg1fL3Va8Z6zViv4ev78PVtkr4-7F-6Aft_wkPaCXh3AAxZE1w0o_X0wAmQvFHtavTjnrvxAe8ebUBffv-2dkn_Zq93ZtLmOqYbVz9E-lyClUon5F8J7Kkt</recordid><startdate>200805</startdate><enddate>200805</enddate><creator>Rautengarten, Carsten</creator><creator>Usadel, Björn</creator><creator>Neumetzler, Lutz</creator><creator>Hartmann, Jürgen</creator><creator>Büssis, Dirk</creator><creator>Altmann, Thomas</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell Science</general><scope>FBQ</scope><scope>IQODW</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>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200805</creationdate><title>subtilisin-like serine protease essential for mucilage release from Arabidopsis seed coats</title><author>Rautengarten, Carsten ; Usadel, Björn ; Neumetzler, Lutz ; Hartmann, Jürgen ; Büssis, Dirk ; Altmann, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5697-421d38a3fb0bb036b2e45735c9eeb0722150155e8d40f8af273fcc4f0b35800e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adhesives - metabolism</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - growth & development</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Arabidopsis thaliana</topic><topic>Biological and medical sciences</topic><topic>Botany</topic><topic>Carboxylic Ester Hydrolases - genetics</topic><topic>Carboxylic Ester Hydrolases - metabolism</topic><topic>cell wall</topic><topic>Cellular biology</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Plant</topic><topic>Germination and dormancy</topic><topic>Hexuronic Acids - metabolism</topic><topic>mucilage</topic><topic>Mutation</topic><topic>pectin methylesterase</topic><topic>pectinesterase</topic><topic>Plant physiology and development</topic><topic>Plants, Genetically Modified</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Rhamnose - metabolism</topic><topic>seed coat</topic><topic>Seeds</topic><topic>Seeds - genetics</topic><topic>Seeds - growth & development</topic><topic>Seeds - metabolism</topic><topic>Serine Endopeptidases - genetics</topic><topic>Serine Endopeptidases - metabolism</topic><topic>subtilase</topic><topic>Subtilisin - genetics</topic><topic>Subtilisin - metabolism</topic><topic>testa</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rautengarten, Carsten</creatorcontrib><creatorcontrib>Usadel, Björn</creatorcontrib><creatorcontrib>Neumetzler, Lutz</creatorcontrib><creatorcontrib>Hartmann, Jürgen</creatorcontrib><creatorcontrib>Büssis, Dirk</creatorcontrib><creatorcontrib>Altmann, Thomas</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rautengarten, Carsten</au><au>Usadel, Björn</au><au>Neumetzler, Lutz</au><au>Hartmann, Jürgen</au><au>Büssis, Dirk</au><au>Altmann, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>subtilisin-like serine protease essential for mucilage release from Arabidopsis seed coats</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2008-05</date><risdate>2008</risdate><volume>54</volume><issue>3</issue><spage>466</spage><epage>480</epage><pages>466-480</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>During Arabidopsis seed development large quantities of mucilage, composed of pectins, are deposited into the apoplast underneath the outer wall of the seed coat. Upon imbibition of mature seeds, the stored mucilage expands through hydration and breaks the outer cell wall that encapsulates the whole seed. Mutant seeds carrying loss-of-function alleles of AtSBT1.7 that encodes one of 56 Arabidopsis thaliana subtilisin-like serine proteases (subtilases) do not release mucilage upon hydration. Microscopic analysis of the mutant seed coat revealed no visible structural differences compared with wild-type seeds. Weakening of the outer primary wall using cation chelators triggered mucilage release from the seed coats of mutants. However, in contrast to mature wild-type seeds, the mutant's outer cell walls did not rupture at the radial walls of the seed coat epidermal cells, but instead opened at the chalazal end of the seed, and were released in one piece. In atsbt1.7, the total rhamnose and galacturonic acid contents, representing the backbone of mucilage, remained unchanged compared with wild-type seeds. Thus, extrusion and solubility, but not the initial deposition of mucilage, are affected in atsbt1.7 mutants. AtSBT1.7 is localized in the developing seed coat, indicating a role in testa development or maturation. The altered mode of rupture of the outer seed coat wall and mucilage release indicate that AtSBT1.7 triggers the accumulation, and/or activation, of cell wall modifying enzymes necessary either for the loosening of the outer primary cell wall, or to facilitate swelling of the mucilage, as indicated by elevated pectin methylesterase activity in developing atsbt1.7 mutant seeds.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>18266922</pmid><doi>10.1111/j.1365-313X.2008.03437.x</doi><tpages>15</tpages></addata></record> |
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subjects | Adhesives - metabolism Arabidopsis - genetics Arabidopsis - growth & development Arabidopsis - metabolism Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Arabidopsis thaliana Biological and medical sciences Botany Carboxylic Ester Hydrolases - genetics Carboxylic Ester Hydrolases - metabolism cell wall Cellular biology Enzymes Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Plant Germination and dormancy Hexuronic Acids - metabolism mucilage Mutation pectin methylesterase pectinesterase Plant physiology and development Plants, Genetically Modified Reverse Transcriptase Polymerase Chain Reaction Rhamnose - metabolism seed coat Seeds Seeds - genetics Seeds - growth & development Seeds - metabolism Serine Endopeptidases - genetics Serine Endopeptidases - metabolism subtilase Subtilisin - genetics Subtilisin - metabolism testa |
title | subtilisin-like serine protease essential for mucilage release from Arabidopsis seed coats |
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