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Perception and response to the hormone auxin is critical to plant growth and development. Expression of auxin-response genes is tightly regulated via known mechanisms of both activation and repression. Across the plant lineage, auxin-response gene induction is performed by AUXIN-REPSONSE FACTOR (ARF) activating transcription factors. Conversely, AUXIN/INDOLE ACETIC ACID proteins repress expression. Studies of gain-of-function constitutive-repression lines and ARF loss-of-function mutants have advanced the field. Yet, there is a need for a comparative study of aberrant auxin-signaling mutants to understand the developmental consequences of constitutive repression versus the absence of auxin-mediated gene induction. Using CRISPR/Cas9 gene-editing tools, we mutated each activating ARF gene in the model bryophyte, Physcomitrium patens. The resulting septuple loss-of-function mutant line (arfasept) has severe developmental phenotypes and a diminished ability to respond to exogenous auxin. However, phenotypic analysis revealed that the arfasept line is not as severely affected as the constitutive-repression lines. Expression analysis of several auxin-response genes demonstrate that auxin-mediated gene induction is abolished in both arfasept and constitutive-repression lines but that basal expression levels are higher in the arfasept lines. Our results suggest that the expression of auxin-regulated genes important for developmental progression is maintained, albeit at reduced levels, in the absence of ARFs.
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http://dx.doi.org/10.1093/jxb/eraf183 | DOI Listing |
Plants (Basel)
August 2025
Research Institute of Oil Tea Camellia, Hunan Academy of Forestry, Changsha 410004, China.
Grafting serves as a crucial propagation technique for superior varieties, where rootstock-scion compatibility significantly determines survival and growth performance. To systematically evaluate grafting compatibility in this economically important woody oil crop, we examined 15 rootstock-scion combinations using 'Xianglin 210' as the scion, assessing growth traits and conducting physiological assays (enzymatic activities of SOD and POD and levels of ROS and IAA) at multiple timepoints (0-32 days post-grafting). The results demonstrated that Comb.
View Article and Find Full Text PDFPlant Physiol
August 2025
Department of Biotechnology, Agricultural University of Athens, Iera Odos 75, Athens 118 55, Greece.
Cell expansion relies on turgor pressure and acidification-dependent loosening of the rigid cell wall. Distinct cell surface-based and intracellular auxin signaling pathways synergistically activate plasma membrane H+-ATPases, acidifying the apoplast, a prerequisite for cell elongation. Unlike in shoots, auxin inhibits cell elongation in roots.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Cell and Developmental Biology, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0116.
The PINOID (PID) protein kinase is required for flower initiation in Arabidopsis. The mutants fail to initiate flowers on inflorescences, a phenotype that is mimicked by disrupting either the ( gene family or (). Both PID and NPY1 have been reported to positively modulate PIN-mediated polar auxin transport.
View Article and Find Full Text PDFPlant J
August 2025
Institute of Science and Technology Austria, 3400, Klosterneuburg, Austria.
Very long-chain fatty acids (VLCFAs), being constituents of different types of lipids, are critical factors in plant development, presumably due to their impact on the endomembrane system. The VLCFAs are synthesized in the endoplasmic reticulum by a heterotetrameric enzymatic complex including β-ketoacyl CoA reductase 1 (KCR1), whose mutant is lethal. Here, we describe the ectopic shoot meristems (esm) mutant, a viable kcr1 allele presumably affecting surface properties of the KCR1 protein.
View Article and Find Full Text PDFCell Rep
August 2025
Shanghai Collaborative Innovation Center of Agri-Seeds, Joint Center for Single Cell Biology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China; Guangdong Laboratory for Lingnan Modern Agriculture, Guangdong Basic Research Center of Excellence for Precise Breed
Auxin regulates various aspects of plant growth and development by modulating the transcription of target genes through the degradation of auxin/indole-3-acetic acid (Aux/IAA) repressors via the 26S proteasome. Proteasome regulator 1 (PTRE1), a positive regulator of proteasome activity, has been implicated in auxin-mediated proteasome suppression; however, the mechanism by which auxin modulates PTRE1 function remains unclear. Here, we demonstrate that auxin promotes the interaction between germin-like protein 1 (GLP1) and PTRE1, facilitating PTRE1 retention at the plasma membrane.
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