skip to main content

Attention:

The NSF Public Access Repository (PAR) system and access will be unavailable from 11:00 PM ET on Thursday, January 16 until 2:00 AM ET on Friday, January 17 due to maintenance. We apologize for the inconvenience.


Title: AINTEGUMENTA and redundant AINTEGUMENTA-LIKE6 are required for bract outgrowth in Arabidopsis
Abstract

Plants consist of fundamental units of growth called phytomers (leaf or bract, axillary bud, node, and internode), which are repeated and modified throughout shoot development to give plants plasticity for survival and adaptation. One phytomer modification is the suppression or outgrowth of bracts, the leaves subtending the flowers. The floral meristem identity regulator LEAFY (LFY) and the organ boundary genes BLADE-ON-PETIOLE1 (BOP1) and BOP2 have been shown to suppress bract development in Arabidopsis, as mutations in these genes result in bract outgrowth. However, much less is known about the mechanisms that promote bract outgrowth in Arabidopsis mutants such as these. Further understanding of this mechanism may provide a potential tool for modifying leaf development. Here, we showed that the MADS-box genes SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1), FRUITFUL (FUL), and AGAMOUS-LIKE24 (AGL24) play more important roles than BOP1/2 and LFY in bract suppression, and that AINTEGUMENTA (ANT) and the partially redundant AINTEGUMENTA-LIKE6 (AIL6) are necessary for bract outgrowth in these mutant backgrounds. We also demonstrated that misexpression of AIL6 alone is sufficient for bract outgrowth. Our data reveal a mechanism for bract suppression and outgrowth and provide insight into phytomer plasticity.

 
more » « less
PAR ID:
10522537
Author(s) / Creator(s):
; ;
Publisher / Repository:
Oxford University Press
Date Published:
Journal Name:
Journal of Experimental Botany
Volume:
75
Issue:
13
ISSN:
0022-0957
Format(s):
Medium: X Size: p. 3920-3931
Size(s):
p. 3920-3931
Sponsoring Org:
National Science Foundation
More Like this
  1. Summary

    l‐Tyrosine is an essential aromatic amino acid required for the synthesis of proteins and a diverse array of plant natural products; however, little is known on how the levels of tyrosine are controlledin plantaand linked to overall growth and development. Most plants synthesize tyrosine by TyrA arogenate dehydrogenases, which are strongly feedback‐inhibited by tyrosine and encoded byTyrA1andTyrA2genes inArabidopsis thaliana. While TyrA enzymes have been extensively characterized at biochemical levels, theirin plantafunctions remain uncertain. Here we found thatTyrA1suppression reduces seed yield due to impaired anther dehiscence, whereasTyrA2knockout leads to slow growth with reticulate leaves. Thetyra2mutant phenotypes were exacerbated byTyrA1suppression and rescued by the expression ofTyrA2,TyrA1or tyrosine feeding. Low‐light conditions synchronized thetyra2and wild‐type growth, and ameliorated thetyra2leaf reticulation. After shifting to normal light,tyra2transiently decreased tyrosine and subsequently increased aspartate before the appearance of the leaf phenotypes. Overexpression of the deregulated TyrA enzymes led to hyper‐accumulation of tyrosine, which was also accompanied by elevated aspartate and reticulate leaves. These results revealed that TyrA1 and TyrA2 have distinct and overlapping functions in flower and leaf development, respectively, and that imbalance of tyrosine, caused by altered TyrA activity and regulation, impacts growth and development of Arabidopsis. The findings provide critical bases for improving the production of tyrosine and its derived natural products, and further elucidating the coordinated metabolic and physiological processes to maintain tyrosine levels in plants.

     
    more » « less
  2. Abstract

    Plants monitor seasonal cues to optimize reproductive success by tuning onset of reproduction and inflorescence architecture. TERMINAL FLOWER 1 (TFL1) and FLOWERING LOCUS T (FT) and their orthologs antagonistically regulate these life history traits, yet their mechanism of action, antagonism and targets remain poorly understood. Here, we show that TFL1 is recruited to thousands of loci by the bZIP transcription factor FD. We identify the master regulator of floral fate,LEAFY(LFY) as a target under dual opposite regulation by TFL1 and FT and uncover a pivotal role of FT in promoting flower fate viaLFYupregulation. We provide evidence that the antagonism between FT and TFL1 relies on competition for chromatin-bound FD at shared target loci. Direct TFL1-FD regulated target genes identify this complex as a hub for repressing both master regulators of reproductive development and endogenous signalling pathways. Our data provide mechanistic insight into how TFL1-FD sculpt inflorescence architecture, a trait important for reproductive success, plant architecture and yield.

     
    more » « less
  3. Organ initiation from the shoot apical meristem first gives rise to leaves during vegetative development and then flowers during reproductive development.LEAFY(LFY) is activated after floral induction and together with other factors promotes the floral program. LFY functions redundantly with APETALA1 (AP1) to activate the class B genesAPETALA3(AP3) andPISTILLATA(PI), the class C geneAGAMOUS(AG), and the class E geneSEPALLATA3, which leads to the specification of stamens and carpels, the reproductive organs of flowers. Molecular and genetic networks that control the activation ofAP3,PI,andAGin flowers have been well studied; however, much less is known about how these genes are repressed in leaves and how their repression is lifted in flowers. Here, we showed that two genes encodingArabidopsisC2H2 ZINC FINGER PROTEIN (ZFP) transcription factors, ZP1 and ZFP8, act redundantly to directly repressAP3,PI,andAGin leaves. AfterLFYandAP1are activated in floral meristems, they down-regulateZP1andZFP8directly to lift the repression onAP3,PI,andAG. Our results reveal a mechanism for how floral homeotic genes are repressed and derepressed before and after floral induction.

     
    more » « less
  4. Abstract

    microRNAs are powerful regulators of growth, development, and stress responses in plants. TheArabidopsis thalianamicroRNAmiR167was previously found to regulate diverse processes including flower development, root development, and response to osmotic stress by controlling the patterns of expression of its target genesAUXIN RESPONSE FACTOR 6 (ARF6), ARF8,andIAA‐Ala RESISTANT 3. Here, we report thatmiR167also modulates defense against pathogens throughARF6andARF8.miR167is differentially expressed in response to the bacterial pathogenPseudomonas syringae, and overexpression ofmiR167confers very high levels of resistance. This resistance appears to be due to suppression of auxin responses and is partially dependent upon salicylic acid signaling, and also depends upon altered stomatal behavior in these plants. Closure of stomata upon the detection ofP. syringaeis an important aspect of the basal defense response, as it prevents bacterial cells from entering the leaf interior and causing infection. Plants overexpressingmiR167constitutively maintain small stomatal apertures, resulting in very high resistance when the pathogen is inoculated onto the leaf surface. Additionally, the systemic acquired resistance (SAR) response is severely compromised in plants overexpressingmiR167,in agreement with previous work showing that the activation of SAR requires intact auxin signaling responses. This work highlights a new role formiR167, and also emphasizes the importance of hormonal balance in short‐ and long‐term defense and of stomata as an initial barrier to pathogen entry.

     
    more » « less
  5. Abstract

    The dominance of flowering plants on earth is owed largely to the evolution of maternal tissues such as fruit and seedcoat that protect and disseminate the seeds. The mechanism of how fertilization triggers the development of these specialized maternal tissues is not well understood. A key event is the induction of auxin synthesis in the endosperm, and the mobile auxin subsequently stimulates seedcoat and fruit development. However, the regulatory mechanism of auxin synthesis in the endosperm remains unknown. Here, we show that a type I MADS box geneAGL62is required for the activation of auxin synthesis in the endosperm in bothFragaria vesca, a diploid strawberry, and in Arabidopsis. Several strawberryFveATHBgenes were identified as downstream targets ofFveAGL62and act to repress auxin biosynthesis. In this work, we identify a key mechanism for auxin induction to mediate fertilization success, a finding broadly relevant to flowering plants.

     
    more » « less