Gibberellic acid induces non-Kranz anatomy with C4-like biochemical traits in the amphibious sedge Eleocharis vivipara
Main conclusion Gibberellic acid induces photosynthetic tissues with non-Kranz anatomy and C 4 -like biochemical traits in terrestrial-form plants of Eleocharis vivipara . This suggests that the structural and biochemical traits are independently regulated. The amphibious leafless sedge, Eleocharis...
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description | Main conclusion
Gibberellic acid induces photosynthetic tissues with non-Kranz anatomy and C
4
-like biochemical traits in terrestrial-form plants of
Eleocharis vivipara
. This suggests that the structural and biochemical traits are independently regulated.
The amphibious leafless sedge,
Eleocharis vivipara
Link, develops culms (photosynthetic organs) with C
4
-like traits and Kranz anatomy under terrestrial conditions, and C
3
traits and non-Kranz anatomy under submerged conditions. The conversion from C
3
mode to C
4
-like mode in
E. vivipara
is reportedly mediated by abscisic acid. Here, we investigated the effects of gibberellic acid (GA) on the differentiation of anatomical and photosynthetic traits because GA is involved in heterophylly in aquatic plants. When 100 µM GA was sprayed on terrestrial plants, the newly developed culms had non-Kranz anatomy in the basal part and Kranz-like anatomy in the upper part. In the basal part, the mesophyll cells were well developed, whereas the Kranz (bundle sheath) cells were reduced and contained few chloroplasts and mitochondria. Stomatal frequency was lower in the basal part than in the upper part. Nevertheless, these tissues had abundant accumulation and high activities of C
4
photosynthetic enzymes and had C
4
-like δ
13
C values, as seen in the culms of the terrestrial form. When submerged plants were grown under water containing GA-biosynthesis inhibitors (uniconazole or paclobutrazol), the new culms had Kranz anatomy. The culms developed under paclobutrazol had the C
3
pattern of cellular accumulation of photosynthetic enzymes. These data suggest that GA induces production of photosynthetic tissues with non-Kranz anatomy in terrestrial plants of
E. vivipara
, without concomitant expression of C
3
biochemical traits. The data also suggest that the differentiation of C
4
structural and biochemical traits is regulated independently. |
doi_str_mv | 10.1007/s00425-021-03662-9 |
format | Article |
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Gibberellic acid induces photosynthetic tissues with non-Kranz anatomy and C
4
-like biochemical traits in terrestrial-form plants of
Eleocharis vivipara
. This suggests that the structural and biochemical traits are independently regulated.
The amphibious leafless sedge,
Eleocharis vivipara
Link, develops culms (photosynthetic organs) with C
4
-like traits and Kranz anatomy under terrestrial conditions, and C
3
traits and non-Kranz anatomy under submerged conditions. The conversion from C
3
mode to C
4
-like mode in
E. vivipara
is reportedly mediated by abscisic acid. Here, we investigated the effects of gibberellic acid (GA) on the differentiation of anatomical and photosynthetic traits because GA is involved in heterophylly in aquatic plants. When 100 µM GA was sprayed on terrestrial plants, the newly developed culms had non-Kranz anatomy in the basal part and Kranz-like anatomy in the upper part. In the basal part, the mesophyll cells were well developed, whereas the Kranz (bundle sheath) cells were reduced and contained few chloroplasts and mitochondria. Stomatal frequency was lower in the basal part than in the upper part. Nevertheless, these tissues had abundant accumulation and high activities of C
4
photosynthetic enzymes and had C
4
-like δ
13
C values, as seen in the culms of the terrestrial form. When submerged plants were grown under water containing GA-biosynthesis inhibitors (uniconazole or paclobutrazol), the new culms had Kranz anatomy. The culms developed under paclobutrazol had the C
3
pattern of cellular accumulation of photosynthetic enzymes. These data suggest that GA induces production of photosynthetic tissues with non-Kranz anatomy in terrestrial plants of
E. vivipara
, without concomitant expression of C
3
biochemical traits. The data also suggest that the differentiation of C
4
structural and biochemical traits is regulated independently.</description><identifier>ISSN: 0032-0935</identifier><identifier>EISSN: 1432-2048</identifier><identifier>DOI: 10.1007/s00425-021-03662-9</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Abscisic acid ; Agriculture ; Anatomy ; Aquatic plants ; Bioaccumulation ; Biochemistry ; Biomedical and Life Sciences ; Biosynthesis ; Chloroplasts ; Differentiation ; Ecology ; Eleocharis vivipara ; Enzymes ; Forestry ; Gibberellic acid ; Life Sciences ; Mesophyll ; Mitochondria ; Organs ; Original Article ; Pesticides ; Photosynthesis ; Plant Sciences ; Sheaths ; Stomata ; Submerged plants ; Terrestrial environments</subject><ispartof>Planta, 2021-07, Vol.254 (1), p.10-10, Article 10</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2679-fd77e72a38d8cf87bbb75201f877f7fc92c988c7070039d9a37f07ca453b0ac23</citedby><cites>FETCH-LOGICAL-c2679-fd77e72a38d8cf87bbb75201f877f7fc92c988c7070039d9a37f07ca453b0ac23</cites><orcidid>0000-0002-7176-1283</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00425-021-03662-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00425-021-03662-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Suizu, Yoshinobu</creatorcontrib><creatorcontrib>Takao, Kazuya</creatorcontrib><creatorcontrib>Ueno, Osamu</creatorcontrib><title>Gibberellic acid induces non-Kranz anatomy with C4-like biochemical traits in the amphibious sedge Eleocharis vivipara</title><title>Planta</title><addtitle>Planta</addtitle><description>Main conclusion
Gibberellic acid induces photosynthetic tissues with non-Kranz anatomy and C
4
-like biochemical traits in terrestrial-form plants of
Eleocharis vivipara
. This suggests that the structural and biochemical traits are independently regulated.
The amphibious leafless sedge,
Eleocharis vivipara
Link, develops culms (photosynthetic organs) with C
4
-like traits and Kranz anatomy under terrestrial conditions, and C
3
traits and non-Kranz anatomy under submerged conditions. The conversion from C
3
mode to C
4
-like mode in
E. vivipara
is reportedly mediated by abscisic acid. Here, we investigated the effects of gibberellic acid (GA) on the differentiation of anatomical and photosynthetic traits because GA is involved in heterophylly in aquatic plants. When 100 µM GA was sprayed on terrestrial plants, the newly developed culms had non-Kranz anatomy in the basal part and Kranz-like anatomy in the upper part. In the basal part, the mesophyll cells were well developed, whereas the Kranz (bundle sheath) cells were reduced and contained few chloroplasts and mitochondria. Stomatal frequency was lower in the basal part than in the upper part. Nevertheless, these tissues had abundant accumulation and high activities of C
4
photosynthetic enzymes and had C
4
-like δ
13
C values, as seen in the culms of the terrestrial form. When submerged plants were grown under water containing GA-biosynthesis inhibitors (uniconazole or paclobutrazol), the new culms had Kranz anatomy. The culms developed under paclobutrazol had the C
3
pattern of cellular accumulation of photosynthetic enzymes. These data suggest that GA induces production of photosynthetic tissues with non-Kranz anatomy in terrestrial plants of
E. vivipara
, without concomitant expression of C
3
biochemical traits. The data also suggest that the differentiation of C
4
structural and biochemical traits is regulated independently.</description><subject>Abscisic acid</subject><subject>Agriculture</subject><subject>Anatomy</subject><subject>Aquatic plants</subject><subject>Bioaccumulation</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biosynthesis</subject><subject>Chloroplasts</subject><subject>Differentiation</subject><subject>Ecology</subject><subject>Eleocharis vivipara</subject><subject>Enzymes</subject><subject>Forestry</subject><subject>Gibberellic acid</subject><subject>Life Sciences</subject><subject>Mesophyll</subject><subject>Mitochondria</subject><subject>Organs</subject><subject>Original Article</subject><subject>Pesticides</subject><subject>Photosynthesis</subject><subject>Plant Sciences</subject><subject>Sheaths</subject><subject>Stomata</subject><subject>Submerged plants</subject><subject>Terrestrial environments</subject><issn>0032-0935</issn><issn>1432-2048</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU9LAzEQxYMoWKtfwFPAi5fobLK72Ryl1CoWvOg5zGazber-qcm2Uj-9qRUED55mYH7vMY9HyGUCNwmAvA0AKc8Y8ISByHPO1BEZJangjENaHJMRQNxBieyUnIWwAohHKUdkO3Nlab1tGmcoGldR11UbYwPt-o49eew-KXY49O2OfrhhSScpa9ybpaXrzdK2zmBDB49uCFFJh6Wl2K6XLp43gQZbLSydNjay6F2gW7d1a_R4Tk5qbIK9-Jlj8no_fZk8sPnz7HFyN2eG51KxupLSSo6iqApTF7IsS5lxSOIqa1kbxY0qCiNBxnyqUihkDdJgmokS0HAxJtcH37Xv3zc2DLp1wcS02Nn4oOZZmia5SPMsold_0FW_8V38bk-JQuWc7w35gTK-D8HbWq-9a9HvdAJ6X4U-VKFjFfq7Cq2iSBxEIcLdwvpf639UX6kcjFg</recordid><startdate>20210701</startdate><enddate>20210701</enddate><creator>Suizu, Yoshinobu</creator><creator>Takao, Kazuya</creator><creator>Ueno, Osamu</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7176-1283</orcidid></search><sort><creationdate>20210701</creationdate><title>Gibberellic acid induces non-Kranz anatomy with C4-like biochemical traits in the amphibious sedge Eleocharis vivipara</title><author>Suizu, Yoshinobu ; Takao, Kazuya ; Ueno, Osamu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2679-fd77e72a38d8cf87bbb75201f877f7fc92c988c7070039d9a37f07ca453b0ac23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Abscisic acid</topic><topic>Agriculture</topic><topic>Anatomy</topic><topic>Aquatic plants</topic><topic>Bioaccumulation</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biosynthesis</topic><topic>Chloroplasts</topic><topic>Differentiation</topic><topic>Ecology</topic><topic>Eleocharis vivipara</topic><topic>Enzymes</topic><topic>Forestry</topic><topic>Gibberellic acid</topic><topic>Life Sciences</topic><topic>Mesophyll</topic><topic>Mitochondria</topic><topic>Organs</topic><topic>Original Article</topic><topic>Pesticides</topic><topic>Photosynthesis</topic><topic>Plant Sciences</topic><topic>Sheaths</topic><topic>Stomata</topic><topic>Submerged plants</topic><topic>Terrestrial environments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suizu, Yoshinobu</creatorcontrib><creatorcontrib>Takao, Kazuya</creatorcontrib><creatorcontrib>Ueno, Osamu</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Planta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suizu, Yoshinobu</au><au>Takao, Kazuya</au><au>Ueno, Osamu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gibberellic acid induces non-Kranz anatomy with C4-like biochemical traits in the amphibious sedge Eleocharis vivipara</atitle><jtitle>Planta</jtitle><stitle>Planta</stitle><date>2021-07-01</date><risdate>2021</risdate><volume>254</volume><issue>1</issue><spage>10</spage><epage>10</epage><pages>10-10</pages><artnum>10</artnum><issn>0032-0935</issn><eissn>1432-2048</eissn><abstract>Main conclusion
Gibberellic acid induces photosynthetic tissues with non-Kranz anatomy and C
4
-like biochemical traits in terrestrial-form plants of
Eleocharis vivipara
. This suggests that the structural and biochemical traits are independently regulated.
The amphibious leafless sedge,
Eleocharis vivipara
Link, develops culms (photosynthetic organs) with C
4
-like traits and Kranz anatomy under terrestrial conditions, and C
3
traits and non-Kranz anatomy under submerged conditions. The conversion from C
3
mode to C
4
-like mode in
E. vivipara
is reportedly mediated by abscisic acid. Here, we investigated the effects of gibberellic acid (GA) on the differentiation of anatomical and photosynthetic traits because GA is involved in heterophylly in aquatic plants. When 100 µM GA was sprayed on terrestrial plants, the newly developed culms had non-Kranz anatomy in the basal part and Kranz-like anatomy in the upper part. In the basal part, the mesophyll cells were well developed, whereas the Kranz (bundle sheath) cells were reduced and contained few chloroplasts and mitochondria. Stomatal frequency was lower in the basal part than in the upper part. Nevertheless, these tissues had abundant accumulation and high activities of C
4
photosynthetic enzymes and had C
4
-like δ
13
C values, as seen in the culms of the terrestrial form. When submerged plants were grown under water containing GA-biosynthesis inhibitors (uniconazole or paclobutrazol), the new culms had Kranz anatomy. The culms developed under paclobutrazol had the C
3
pattern of cellular accumulation of photosynthetic enzymes. These data suggest that GA induces production of photosynthetic tissues with non-Kranz anatomy in terrestrial plants of
E. vivipara
, without concomitant expression of C
3
biochemical traits. The data also suggest that the differentiation of C
4
structural and biochemical traits is regulated independently.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00425-021-03662-9</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7176-1283</orcidid></addata></record> |
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source | SpringerLink Journals - AutoHoldings |
subjects | Abscisic acid Agriculture Anatomy Aquatic plants Bioaccumulation Biochemistry Biomedical and Life Sciences Biosynthesis Chloroplasts Differentiation Ecology Eleocharis vivipara Enzymes Forestry Gibberellic acid Life Sciences Mesophyll Mitochondria Organs Original Article Pesticides Photosynthesis Plant Sciences Sheaths Stomata Submerged plants Terrestrial environments |
title | Gibberellic acid induces non-Kranz anatomy with C4-like biochemical traits in the amphibious sedge Eleocharis vivipara |
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