2020
DOI: 10.7554/elife.51787
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Direct ETTIN-auxin interaction controls chromatin states in gynoecium development

Abstract: Hormonal signalling in animals often involves direct transcription factor-hormone interactions that modulate gene expression. In contrast, plant hormone signalling is most commonly based on de-repression via the degradation of transcriptional repressors. Recently, we uncovered a non-canonical signalling mechanism for the plant hormone auxin whereby auxin directly affects the activity of the atypical auxin response factor (ARF), ETTIN towards target genes without the requirement for protein degradation. Here we… Show more

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Cited by 54 publications
(65 citation statements)
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“…For example, the atypical ARF ETTIN (ETT) cannot recruit AUX/ IAA adaptors and instead directly recruits TPLs, via a BRD repression domain, to repress auxin target genes. Remarkably, ETT also acts as an auxin receptor, and auxin binding by ETT disrupts the ETT-TPL interaction, leading to de-repression of ETT targets (Kuhn et al, 2020).…”
Section: Hormone Signallingmentioning
confidence: 99%
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“…For example, the atypical ARF ETTIN (ETT) cannot recruit AUX/ IAA adaptors and instead directly recruits TPLs, via a BRD repression domain, to repress auxin target genes. Remarkably, ETT also acts as an auxin receptor, and auxin binding by ETT disrupts the ETT-TPL interaction, leading to de-repression of ETT targets (Kuhn et al, 2020).…”
Section: Hormone Signallingmentioning
confidence: 99%
“…All genetic components of the canonical [ARF]‐[AUX/IAA]‐[TPL/TPR] mechanism regulating auxin responses are conserved from Charophyte algae through to the angiosperms (Flores‐Sandoval et al, 2015; Martin‐Arevalillo et al, 2019), although it remains to be determined whether the mechanism is functionally conserved. However, additional non‐canonical auxin signalling mechanisms that utilise TPL corepressors have been identified (Causier et al, 2012a,b; Kuhn et al, 2020). For example, the atypical ARF ETTIN (ETT) cannot recruit AUX/IAA adaptors and instead directly recruits TPLs, via a BRD repression domain, to repress auxin target genes.…”
Section: Tpl/tprs Are Recruited Into Diverse Biological Processesmentioning
confidence: 99%
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“…This in turn, releases repression of Auxin Response Element-(ARE)-containing promoters, simply put, as a consequence of derepressed AUXIN RESPONSE FACTOR (ARF) transcription factors no longer dimerizing with Aux/IAAs [ 36 ]. Alternate auxin sensing mechanisms have been identified, which involves activity of plasma membrane-resident TRANSMEMBRANE KINASE (TMK) proteins [ 37 , 38 , 39 ] as well as hormone sensing via the ARF3/ETTIN transcriptional regulator [ 40 , 41 ]. Modes of auxin perception via these pathways are still only partially resolved and matter of discussion [ 42 , 43 ], but downstream signaling events have been characterized to some extent.…”
Section: Auxinmentioning
confidence: 99%
“…Accordingly, TPL, TPR2 and TPR4 acting together seem to regulate the DCL1 and SERRATE expression, while TPR4 alone may be involved in the repression of HEN1. The gene silencing complexes commonly consist of different TPL/TPR proteins [65,66]. However, recently, a monomeric form of TPL was found to be sufficient to cause an intense transcriptional repression in plants [67].…”
Section: Agl15 Together With the Tpl/tpr Corepressors Transcriptionalmentioning
confidence: 99%