2013
Single-cell-based system to monitor carrier driven cellular auxin homeostasis
BARBEZ, Elke; Martina LANKOVA; Marketa PAREZOVA; Alexis MAIZEL; Eva ZAŽÍMALOVÁ et al.Základní údaje
Originální název
Single-cell-based system to monitor carrier driven cellular auxin homeostasis
Autoři
BARBEZ, Elke; Martina LANKOVA; Marketa PAREZOVA; Alexis MAIZEL; Eva ZAŽÍMALOVÁ; Jan PETRASEK; Jiří FRIML a Jurgen KLEINE-VEHN
Vydání
BMC Plant Biology, London, BioMed Central Ltd. 2013, 1471-2229
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10611 Plant sciences, botany
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.942
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14740/13:00072091
Organizační jednotka
Středoevropský technologický institut
UT WoS
Klíčová slova anglicky
Auxin homeostasis; DR5; Auxin carrier; Auxin transport
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 12. 2019 11:44, Mgr. Marie Novosadová Šípková, DiS.
Anotace
V originále
Background: Abundance and distribution of the plant hormone auxin play important roles in plant development. Besides other metabolic processes, various auxin carriers control the cellular level of active auxin and, hence, are major regulators of cellular auxin homeostasis. Despite the developmental importance of auxin transporters, a simple medium-to-high throughput approach to assess carrier activities is still missing. Here we show that carrier driven depletion of cellular auxin correlates with reduced nuclear auxin signaling in tobacco Bright Yellow-2 (BY-2) cell cultures. Results: We developed an easy to use transient single-cell-based system to detect carrier activity. We use the relative changes in signaling output of the auxin responsive promoter element DR5 to indirectly visualize auxin carrier activity. The feasibility of the transient approach was demonstrated by pharmacological and genetic interference with auxin signaling and transport. As a proof of concept, we provide visual evidence that the prominent auxin transport proteins PIN-FORMED (PIN) 2 and PIN5 regulate cellular auxin homeostasis at the plasma membrane and endoplasmic reticulum (ER), respectively. Our data suggest that PIN2 and PIN5 have different sensitivities to the auxin transport inhibitor 1-naphthylphthalamic acid (NPA). Also the putative PIN-LIKES (PILS) auxin carrier activity at the ER is insensitive to NPA in our system, indicating that NPA blocks intercellular, but not intracellular auxin transport. Conclusions: This single-cell-based system is a useful tool by which the activity of putative auxin carriers, such as PINs, PILS and WALLS ARE THIN1 (WAT1), can be indirectly visualized in a medium-to-high throughput manner. Moreover, our single cell system might be useful to investigate also other hormonal signaling pathways, such as cytokinin.
Návaznosti
| ED1.1.00/02.0068, projekt VaV |
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| EE2.3.20.0043, projekt VaV |
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