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Abscisic acid signaling is controlled by a BRANCHED1/HD-ZIP I cascade in Arabidopsis axillary buds
Sunday, 2017/01/15 | 07:12:46

Eduardo González-Grandío, Alice Pajoro, José M. Franco-Zorrilla, Carlos Tarancón, Richard G. H. Immink, and Pilar Cubas

Significance

Shoot-branching patterns affect key aspects of plant life and are important targets for crop breeding. However, we are still ignorant of the genetic mechanisms controlling locally an important decision during branch development: whether the axillary bud grows out to give a lateral shoot or remains dormant. Here we show that the TEOSINTE BRANCHED1, CYCLOIDEA, PCF (TCP) transcriptional regulator BRANCHED1 (BRC1), which acts inside axillary buds, binds and activates three genes encoding Homeodomain leucine zipper (HD-ZIP) transcription factors. These factors, together with BRC1, trigger a cascade leading to local abscisic acid (ABA) accumulation and response, essential for bud dormancy under light-limiting conditions. This finding demonstrates a direct relationship between BRC1 and ABA signaling and places ABA downstream of BRC1 in the control of axillary bud dormancy.

Abstract

Shoot-branching patterns determine key aspects of plant life and are important targets for crop breeding. However, we are still largely ignorant of the genetic networks controlling locally the most important decision during branch development: whether the axillary bud, or branch primordium, grows out to give a lateral shoot or remains dormant. Here we show that, inside the buds, the TEOSINTE BRANCHED1, CYCLOIDEA, PCF (TCP) transcription factor BRANCHED1 (BRC1) binds to and positively regulates the transcription of three related Homeodomain leucine zipper protein (HD-ZIP)-encoding genes: HOMEOBOX PROTEIN 21 (HB21), HOMEOBOX PROTEIN 40 (HB40), and HOMEOBOX PROTEIN 53 (HB53). These three genes, together with BRC1, enhance 9-CIS-EPOXICAROTENOID DIOXIGENASE 3 (NCED3) expression, lead to abscisic acid accumulation, and trigger hormone response, thus causing suppression of bud development. This TCP/HD-ZIP genetic module seems to be conserved in dicot and monocotyledonous species to prevent branching under light-limiting conditions.

 

See: http://www.pnas.org/content/114/2/E245.abstract.html?etoc

PNAS January 3 2017; vol.114; no.2: E245–E254

 

Fig. 1.

BRC1 binds HB21, HB40, and HB53 and controls their transcription. (A and B) HB21, HB40, and HB53 mRNA levels correlate with BRC1 levels. mRNA levels of BRC1, HB21, HB40, and HB53 were analyzed by quantitative PCR in wild-type and brc1 buds treated with W or W+FR light for 8 h (A) and in 7-d-old BRC1ind seedlings after treatment with 10 µM estradiol (B). (C) Schematic representation of reporter constructs transformed into HA:BRC1ind; brc1-2 lines. (D) LUC activity after BRC1 induction with 10 µM estradiol. Levels are relative to t = 0 after induction. Error bars show SEM of eight plants per line for each treatment. (E) Logo representing the frequency matrix of the consensus motif obtained from the alignment of the 10 best-scored binding sites in PBM assays. (F) BRC1-binding motifs in a 1-kb region upstream of the ATG start codon (gray) and genomic regions (exons black, introns white) of HB21, HB40, and HB53. Peak height is proportional to the similarity between sequence and consensus. Numbers indicate the peaks with the highest Rsat score (12). (G) Relative enrichment of GFP:BRC1 binding to sites 1–6. ACT2 was used as a negative control. Error bars show the SEM of three biological replicates (A and B), eight biological replicates (D), and three biological replicates with two technical repetitions (G). Asterisks indicate significant differences (P < 0.05; student’s t-test) between control and treated plants (A) and between untagged BRC1ind and GFP:BRC1ind lines (G).

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