Root growth adaptation under water deficit

Sotelo, Mariana - Cuadrado, Belen - Sainz, Martha - Piriz, Selene - Borsani, Omar

Resumen:

Growth and development of the root system require the coordinated regulation of developmental programs and environmental signals; however, the knowledge about its interconnection is scarce. The balance between cell division, regulated cellular expansion, and differentiation in the root apical meristem directs primary root growth in Arabidopsis. Cellular expansion requires cell wall controlled relaxation, which ensures cell integrity during the expansion process. In field conditions, the root faces different kinds of stress, including osmotic stress. Mutations in the Arabidopsis Tetratrico-peptide Thioredoxin-Like 1 (TTL1) cause hypersensitivity to osmotic stress evidenced by root tip swelling, making it an attractive model to explore how root growth is regulated under osmotic stress conditions. We found that osmotic stress decelerates root growth by reducing first cell elongation in the elongation zone and second the number of cortical cells in the proximal meristem. Using atomic force microscopy, we measure the stiffness of epidermal cell walls in the root elongation zone of ttl1 mutants, and we found that the mean apparent elastic modulus was 448% higher for live Col-0 cell walls than for ttl1 (88.1 ± 2.8 vs. 16.08 ± 6.9 kPa) in plants grown in control conditions. Furthermore, cell walls of epidermal cells in the elongation zone increase their stiffness 87% and 84% for Col-0 and ttl1, respectively, in response to seven days of osmotic stress. These findings suggest that TTL1 may play a role in controlling cell expansion orientation during root growth, necessary for osmotic stress adaptation.


Detalles Bibliográficos
2021
Agencia Nacional de Investigación e Innovación
Root mersitem
Drought
Ciencias Naturales y Exactas
Ciencias Biológicas
Bioquímica y Biología Molecular
Biología del Desarrollo
Inglés
Agencia Nacional de Investigación e Innovación
REDI
https://hdl.handle.net/20.500.12381/3346
https://smbplant.quimica.unam.mx/2021/flash-talk-sessions/
Acceso abierto
Reconocimiento-NoComercial-CompartirIgual 4.0 Internacional. (CC BY-NC-SA)
_version_ 1814959256515903488
author Sotelo, Mariana
author2 Cuadrado, Belen
Sainz, Martha
Piriz, Selene
Borsani, Omar
author2_role author
author
author
author
author_facet Sotelo, Mariana
Cuadrado, Belen
Sainz, Martha
Piriz, Selene
Borsani, Omar
author_role author
bitstream.checksum.fl_str_mv a4ce09f01b5dd771727aa05c73851623
9269022e5d64dbe09d5c88281e3555b8
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
bitstream.url.fl_str_mv https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3346/2/license.txt
https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3346/1/Abstracts-Book-XIX-NPBMBC-2021-web.pdf
collection REDI
dc.creator.none.fl_str_mv Sotelo, Mariana
Cuadrado, Belen
Sainz, Martha
Piriz, Selene
Borsani, Omar
dc.date.accessioned.none.fl_str_mv 2023-12-07T15:21:04Z
dc.date.available.none.fl_str_mv 2023-12-07T15:21:04Z
dc.date.issued.none.fl_str_mv 2021-11-11
dc.description.abstract.none.fl_txt_mv Growth and development of the root system require the coordinated regulation of developmental programs and environmental signals; however, the knowledge about its interconnection is scarce. The balance between cell division, regulated cellular expansion, and differentiation in the root apical meristem directs primary root growth in Arabidopsis. Cellular expansion requires cell wall controlled relaxation, which ensures cell integrity during the expansion process. In field conditions, the root faces different kinds of stress, including osmotic stress. Mutations in the Arabidopsis Tetratrico-peptide Thioredoxin-Like 1 (TTL1) cause hypersensitivity to osmotic stress evidenced by root tip swelling, making it an attractive model to explore how root growth is regulated under osmotic stress conditions. We found that osmotic stress decelerates root growth by reducing first cell elongation in the elongation zone and second the number of cortical cells in the proximal meristem. Using atomic force microscopy, we measure the stiffness of epidermal cell walls in the root elongation zone of ttl1 mutants, and we found that the mean apparent elastic modulus was 448% higher for live Col-0 cell walls than for ttl1 (88.1 ± 2.8 vs. 16.08 ± 6.9 kPa) in plants grown in control conditions. Furthermore, cell walls of epidermal cells in the elongation zone increase their stiffness 87% and 84% for Col-0 and ttl1, respectively, in response to seven days of osmotic stress. These findings suggest that TTL1 may play a role in controlling cell expansion orientation during root growth, necessary for osmotic stress adaptation.
dc.description.sponsorship.none.fl_txt_mv Agencia Nacional de Investigación e Innovación
dc.identifier.anii.es.fl_str_mv FCE_1_2019_1_156503
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12381/3346
dc.identifier.url.none.fl_str_mv https://smbplant.quimica.unam.mx/2021/flash-talk-sessions/
dc.language.iso.none.fl_str_mv eng
dc.relation.uri.none.fl_str_mv https://hdl.handle.net/20.500.12381/3340
https://hdl.handle.net/20.500.12381/3339
https://hdl.handle.net/20.500.12381/3359
https://hdl.handle.net/20.500.12381/3360
dc.rights.*.fl_str_mv Acceso abierto
dc.rights.license.none.fl_str_mv Reconocimiento-NoComercial-CompartirIgual 4.0 Internacional. (CC BY-NC-SA)
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.es.fl_str_mv XIX National Plant Biochemistry and Molecular Biology Congress. XII Symposium Mexico-USA/2nd ASPB Mexico Section
dc.source.none.fl_str_mv reponame:REDI
instname:Agencia Nacional de Investigación e Innovación
instacron:Agencia Nacional de Investigación e Innovación
dc.subject.anii.none.fl_str_mv Ciencias Naturales y Exactas
Ciencias Biológicas
Bioquímica y Biología Molecular
Biología del Desarrollo
dc.subject.es.fl_str_mv Root mersitem
Drought
dc.title.none.fl_str_mv Root growth adaptation under water deficit
dc.type.es.fl_str_mv Documento de conferencia
dc.type.none.fl_str_mv info:eu-repo/semantics/conferenceObject
dc.type.version.es.fl_str_mv Publicado
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
description Growth and development of the root system require the coordinated regulation of developmental programs and environmental signals; however, the knowledge about its interconnection is scarce. The balance between cell division, regulated cellular expansion, and differentiation in the root apical meristem directs primary root growth in Arabidopsis. Cellular expansion requires cell wall controlled relaxation, which ensures cell integrity during the expansion process. In field conditions, the root faces different kinds of stress, including osmotic stress. Mutations in the Arabidopsis Tetratrico-peptide Thioredoxin-Like 1 (TTL1) cause hypersensitivity to osmotic stress evidenced by root tip swelling, making it an attractive model to explore how root growth is regulated under osmotic stress conditions. We found that osmotic stress decelerates root growth by reducing first cell elongation in the elongation zone and second the number of cortical cells in the proximal meristem. Using atomic force microscopy, we measure the stiffness of epidermal cell walls in the root elongation zone of ttl1 mutants, and we found that the mean apparent elastic modulus was 448% higher for live Col-0 cell walls than for ttl1 (88.1 ± 2.8 vs. 16.08 ± 6.9 kPa) in plants grown in control conditions. Furthermore, cell walls of epidermal cells in the elongation zone increase their stiffness 87% and 84% for Col-0 and ttl1, respectively, in response to seven days of osmotic stress. These findings suggest that TTL1 may play a role in controlling cell expansion orientation during root growth, necessary for osmotic stress adaptation.
eu_rights_str_mv openAccess
format conferenceObject
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identifier_str_mv FCE_1_2019_1_156503
instacron_str Agencia Nacional de Investigación e Innovación
institution Agencia Nacional de Investigación e Innovación
instname_str Agencia Nacional de Investigación e Innovación
language eng
network_acronym_str REDI
network_name_str REDI
oai_identifier_str oai:redi.anii.org.uy:20.500.12381/3346
publishDate 2021
reponame_str REDI
repository.mail.fl_str_mv jmaldini@anii.org.uy
repository.name.fl_str_mv REDI - Agencia Nacional de Investigación e Innovación
repository_id_str 9421
rights_invalid_str_mv Reconocimiento-NoComercial-CompartirIgual 4.0 Internacional. (CC BY-NC-SA)
Acceso abierto
spelling Reconocimiento-NoComercial-CompartirIgual 4.0 Internacional. (CC BY-NC-SA)Acceso abiertoinfo:eu-repo/semantics/openAccess2023-12-07T15:21:04Z2023-12-07T15:21:04Z2021-11-11https://hdl.handle.net/20.500.12381/3346FCE_1_2019_1_156503https://smbplant.quimica.unam.mx/2021/flash-talk-sessions/Growth and development of the root system require the coordinated regulation of developmental programs and environmental signals; however, the knowledge about its interconnection is scarce. The balance between cell division, regulated cellular expansion, and differentiation in the root apical meristem directs primary root growth in Arabidopsis. Cellular expansion requires cell wall controlled relaxation, which ensures cell integrity during the expansion process. In field conditions, the root faces different kinds of stress, including osmotic stress. Mutations in the Arabidopsis Tetratrico-peptide Thioredoxin-Like 1 (TTL1) cause hypersensitivity to osmotic stress evidenced by root tip swelling, making it an attractive model to explore how root growth is regulated under osmotic stress conditions. We found that osmotic stress decelerates root growth by reducing first cell elongation in the elongation zone and second the number of cortical cells in the proximal meristem. Using atomic force microscopy, we measure the stiffness of epidermal cell walls in the root elongation zone of ttl1 mutants, and we found that the mean apparent elastic modulus was 448% higher for live Col-0 cell walls than for ttl1 (88.1 ± 2.8 vs. 16.08 ± 6.9 kPa) in plants grown in control conditions. Furthermore, cell walls of epidermal cells in the elongation zone increase their stiffness 87% and 84% for Col-0 and ttl1, respectively, in response to seven days of osmotic stress. These findings suggest that TTL1 may play a role in controlling cell expansion orientation during root growth, necessary for osmotic stress adaptation.Agencia Nacional de Investigación e Innovaciónenghttps://hdl.handle.net/20.500.12381/3340https://hdl.handle.net/20.500.12381/3339https://hdl.handle.net/20.500.12381/3359https://hdl.handle.net/20.500.12381/3360XIX National Plant Biochemistry and Molecular Biology Congress. XII Symposium Mexico-USA/2nd ASPB Mexico Sectionreponame:REDIinstname:Agencia Nacional de Investigación e Innovacióninstacron:Agencia Nacional de Investigación e InnovaciónRoot mersitemDroughtCiencias Naturales y ExactasCiencias BiológicasBioquímica y Biología MolecularBiología del DesarrolloRoot growth adaptation under water deficitDocumento de conferenciaPublicadoinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectUniversidad de la República. Facultad de Agronomía//Ciencias Naturales y Exactas/Ciencias Biológicas/Ciencias Biológicas//Ciencias Naturales y Exactas/Ciencias Biológicas/Bioquímica y Biología Molecular//Ciencias Naturales y Exactas/Ciencias Biológicas/Biología del DesarrolloSotelo, MarianaCuadrado, BelenSainz, MarthaPiriz, SeleneBorsani, OmarLICENSElicense.txtlicense.txttext/plain; charset=utf-84967https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3346/2/license.txta4ce09f01b5dd771727aa05c73851623MD52ORIGINALAbstracts-Book-XIX-NPBMBC-2021-web.pdfAbstracts-Book-XIX-NPBMBC-2021-web.pdfapplication/pdf3882779https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3346/1/Abstracts-Book-XIX-NPBMBC-2021-web.pdf9269022e5d64dbe09d5c88281e3555b8MD5120.500.12381/33462024-01-10 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- Agencia Nacional de Investigación e Innovaciónfalse
spellingShingle Root growth adaptation under water deficit
Sotelo, Mariana
Root mersitem
Drought
Ciencias Naturales y Exactas
Ciencias Biológicas
Bioquímica y Biología Molecular
Biología del Desarrollo
status_str publishedVersion
title Root growth adaptation under water deficit
title_full Root growth adaptation under water deficit
title_fullStr Root growth adaptation under water deficit
title_full_unstemmed Root growth adaptation under water deficit
title_short Root growth adaptation under water deficit
title_sort Root growth adaptation under water deficit
topic Root mersitem
Drought
Ciencias Naturales y Exactas
Ciencias Biológicas
Bioquímica y Biología Molecular
Biología del Desarrollo
url https://hdl.handle.net/20.500.12381/3346
https://smbplant.quimica.unam.mx/2021/flash-talk-sessions/