2016
A Forward Genetic Screen for New Regulators of Auxin-mediated Degradation of Auxin Transport Proteins in Arabidopsis thaliana
ZEMOVÁ, Radka; Marta ZWIEWKA; Agnieszka BIELACH; Hélene ROBERT BOISIVON; Jiří FRIML et al.Základní údaje
Originální název
A Forward Genetic Screen for New Regulators of Auxin-mediated Degradation of Auxin Transport Proteins in Arabidopsis thaliana
Autoři
Vydání
Journal of plant growth regulation, New York, Springer, 2016, 0721-7595
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10605 Developmental biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.073
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14740/16:00087737
Organizační jednotka
Středoevropský technologický institut
UT WoS
EID Scopus
Klíčová slova anglicky
Root development Polar auxin transport Plasma membrane AUX1 PIN2 Vacuolar degradation
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 13. 3. 2018 10:02, Helene Robert Boisivon, Ph.D.
Anotace
V originále
The plant hormone auxin (indole-3-acetic acid) is a major regulator of plant growth and development including embryo and root patterning, lateral organ formation and growth responses to environmental stimuli. Auxin is directionally transported from cell to cell by the action of specific auxin influx [AUXIN-RESISTANT1 (AUX1)] and efflux [PIN-FORMED (PIN)] transport regulators, whose polar, subcellular localizations are aligned with the direction of the auxin flow. Auxin itself regulates its own transport by modulation of the expression and subcellular localization of the auxin transporters. Increased auxin levels promote the transcription of PIN2 and AUX1 genes as well as stabilize PIN proteins at the plasma membrane, whereas prolonged auxin exposure increases the turnover of PIN proteins and their degradation in the vacuole. In this study, we applied a forward genetic approach, to identify molecular components playing a role in the auxin-mediated degradation. We generated EMS-mutagenized Arabidopsis PIN2::PIN2:GFP, AUX1::AUX1:YFP eir1 aux1 populations and designed a screen for mutants with persistently strong fluorescent signals of the tagged PIN2 and AUX1 after prolonged treatment with the synthetic auxin 2,4-dichlorophenoxyacetic acid (2,4-D). This approach yielded novel auxin degradation mutants defective in trafficking and degradation of PIN2 and AUX1 proteins and established a role for auxin-mediated degradation in plant development.
Návaznosti
| ED1.1.00/02.0068, projekt VaV |
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| EE2.3.20.0043, projekt VaV |
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| EE2.3.30.0009, projekt VaV |
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| GA13-40637S, projekt VaV |
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| 3SGA5602, interní kód MU |
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