How plants cope with fast primary root elongation inhibition DOI Creative Commons

Ziwen Qiu,

Cheng Zeng,

Huimin Deng

и другие.

Frontiers in Plant Science, Год журнала: 2023, Номер 14

Опубликована: Май 31, 2023

OPINION article Front. Plant Sci., 31 May 2023Sec. Development and EvoDevo Volume 14 - 2023 | https://doi.org/10.3389/fpls.2023.1187634

Язык: Английский

An auxin research odyssey: 1989–2023 DOI
Jerry D. Cohen, Lucia C. Strader

The Plant Cell, Год журнала: 2024, Номер 36(5), С. 1410 - 1428

Опубликована: Фев. 21, 2024

Abstract The phytohormone auxin is at times called the master regulator of plant processes and has been shown to be a central player in embryo development, establishment polar axis, early aspects seedling growth, as well growth organ formation during later stages development. Plant Cell key, since inception journal, developing an understanding biology. Auxin-regulated control accomplished by both changes levels active hormones sensitivity tissues these concentration changes. In this historical review, we chart research it progressed key areas highlight role played scientific developments. We focus on auxin-responsive genes, transcription factors, reporter constructs, perception, signal transduction processes. Auxin metabolism discussed from development tryptophan auxotrophic mutants, molecular biology conjugate hydrolysis, indole-3-butyric acid transport, steps indole-3-acetic biosynthesis, catabolism, transport. This progress leads expectation more comprehensive systems spatial temporal regulation cellular

Язык: Английский

Процитировано

21

FERONIA-mediated TIR1/AFB2 oxidation stimulates auxin signaling in Arabidopsis DOI

Baiyan Lu,

Shengnan Wang, Hanqian Feng

и другие.

Molecular Plant, Год журнала: 2024, Номер 17(5), С. 772 - 787

Опубликована: Апрель 4, 2024

Язык: Английский

Процитировано

11

Rapid auxin signaling: Unknowns old and new DOI
Lukáš Fiedler, Jìří Friml

Current Opinion in Plant Biology, Год журнала: 2023, Номер 75, С. 102443 - 102443

Опубликована: Сен. 2, 2023

Язык: Английский

Процитировано

21

Calcium-triggered apoplastic ROS bursts balance gravity and mechanical signals to navigate soil DOI Creative Commons
Ivan Kulich,

Dmitrii Vladimirtsev,

Marek Randuch

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2025, Номер unknown

Опубликована: Янв. 8, 2025

Abstract Reactive oxygen species (ROS) have been implicated repeatedly in multiple signaling processes plants but the underlying mechanisms and roles remain enigmatic. Here, we developed live imaging of apoplastic ROS at root surface. Different signals, including auxin, extracellular ATP RALF1 peptide, all induce cytosolic calcium transients bursts. Genetic optogenetic manipulations identified as necessary sufficient for bursts via activation NADPH oxidases RBOHC RBOHF. Apoplastic are not required rather limit gravity-induced bending. Root bending is sensed by stretch-activated channel MCA1 leading to oxidase stretched side. The resulting production stiffens cell wall better soil penetration. thus provides a means balance tissue flexibility stiffness efficiently navigate soil.

Язык: Английский

Процитировано

1

The interplay between extracellular and intracellular auxin signaling in plants DOI Creative Commons
Wenxin Tang, Yongqiang Yu, Tongda Xu

и другие.

Journal of genetics and genomics/Journal of Genetics and Genomics, Год журнала: 2024, Номер unknown

Опубликована: Июль 1, 2024

The phytohormone auxin exerts control over remarkable developmental processes in plants. It moves from cell to cell, resulting the creation of both extracellular and intracellular auxin, which are recognized by distinct receptors. These two signaling systems govern different responses while working together regulate plant development. In this review, we outline latest research advancements unraveling these pathways, encompassing perception transductions. We emphasize interaction between contributes intricate role

Язык: Английский

Процитировано

6

Guanylate cyclase activity of TIR1/AFB auxin receptors in rapid auxin responses DOI Creative Commons
Linlin Qi, Mateusz Kwiatkowski, Ivan Kulich

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2023, Номер unknown

Опубликована: Ноя. 18, 2023

Abstract The major developmental signal in plants, auxin is perceived by TIR1/AFB receptors. It triggers transcriptional reprogramming via well-established canonical mechanism but also elusive rapid, non-transcriptional responses. Here we demonstrate that receptors have, next to recently identified adenylate cyclase, guanylate cyclase activity. Auxin perception activates independently the cAMP and cGMP production TIR1/AFBs vitro increases levels planta with a slow fast dynamics, respectively. Exogenous not application induces rapid cytosolic Ca 2+ transients root growth inhibition, suggesting TIR1/AFB-derived mediates This unprecedented combination of activities hormone receptor provides new paradigm for how single can mediate multitude diverse downstream One-Sentence Summary have activity, whose product,

Язык: Английский

Процитировано

10

Slow and rapid auxin responses in Arabidopsis DOI Creative Commons
Zilin Zhang,

Huihuang Chen,

Shuaiying Peng

и другие.

Journal of Experimental Botany, Год журнала: 2024, Номер 75(18), С. 5471 - 5476

Опубликована: Май 23, 2024

Abstract The TIR1/AFB–Aux/IAA–ARF canonical auxin signaling pathway is widely accepted to (de)active transcriptional regulation, thus controlling auxin-associated developmental processes. However, the theme of a rapid response has emerged since 2018 Auxins and Cytokinin in Plant Development conference. To date, few components have been identified mediate both slow responses, which unveils complexity signaling.

Язык: Английский

Процитировано

4

Indole-3-propionic acid regulates lateral root development by targeting auxin signaling in Arabidopsis DOI Creative Commons
Yue Sun,

Zhisen Yang,

Caoli Zhang

и другие.

iScience, Год журнала: 2024, Номер 27(7), С. 110363 - 110363

Опубликована: Июнь 24, 2024

Indole-3-propionic acid (IPA) is known to be a microbe-derived compound with similar structure the phytohormone auxin (indole-3-acetic acid, IAA). Previous studies reported that IPA exhibited auxin-like bioactivities in plants. However, underlying molecular mechanism not totally understood. Here, we revealed modulated lateral root (LR) development via signaling model plant

Язык: Английский

Процитировано

4

Armadillo Repeat Only Proteins Are Crucial for the Function of Plant CNGC Channels DOI Creative Commons
Ivan Kulich, Denisa Oulehlová,

Dmitrii Vladimirtsev

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2025, Номер unknown

Опубликована: Янв. 7, 2025

Plant cells respond to a wide range of stimuli through intracellular calcium (Ca2+) signaling. Cyclic nucleotide-gated channels (CNGCs) are major class plant Ca2+ channels, with 20 homologs in Arabidopsis. These tetrameric plasma membrane proteins act downstream diverse signals, such as phytohormones, extracellular damage, cell wall integrity or temperature. Here, we identify plant-specific proteins, Armadillo Repeat Only (ARO), essential regulators possibly all CNGCs. Abrogation functional sporophytic AROs results phenotypic pattern strongly reminiscent CNGC dysfunction, including defects root gravitropism, hair growth and morphology, stomatal movement, responses ATP the phytohormone auxin. aro2/3/4 mutants fully resistant toxic effects caused by overexpression colocalize physically interact multiple CNGCs modulate CNGC-dependent currents Xenopus oocytes. Structural modeling site-directed mutagenesis reveal tetramer formation surrounding channel, interacting via its IQ domain. Taken together, don't alone, but larger complex - channelosome, first kind plants.

Язык: Английский

Процитировано

0

BTB/POZ-MATH proteins regulate Arabidopsis seedling development by promoting auxin-independent degradation of the Aux/IAA protein IAA10 DOI

Zhaonan Ban,

Yueh-Ju Hou,

Ellyse Ku

и другие.

PLANT PHYSIOLOGY, Год журнала: 2025, Номер unknown

Опубликована: Апрель 21, 2025

After germination, seedlings undergo etiolated development (skotomorphogenesis), enabling them to grow toward the soil surface. In Arabidopsis (Arabidopsis thaliana), exhibit rapid hypocotyl elongation, apical hook formation, and closed cotyledons protect meristem. this study, we found that high-order mutants in BPM (BTB/POZ-MATH) gene family displayed defects seedling development, characterized by a shorter hypocotyl, early opening, opened dark. BPM1, BPM2, BPM4, BPM5 exhibited distinct expression patterns subcellular localization seedlings. segment assay, bpm showed auxin response, indicating impaired signaling hypocotyl. Expression of reporter DR5:GFP was also altered bpm1,4,5 mutant various tissues compared with wild type. Furthermore, yeast 2-hybrid, bimolecular fluorescence complementation, co-immunoprecipitation assay analyses BPM1 interacts IAA10. Experiments protoplasts indicated promotes IAA10 ubiquitylation degradation, which supported greater protein accumulation background. addition, overexpression resulted phenotypes similar those mutants, BPMs may target Aux/IAA proteins for degradation. Overall, our findings shed light on key roles during development.

Язык: Английский

Процитировано

0