TY - JOUR A1 - Lohmann, Daniel A1 - Stacey, Nicola A1 - Breuninger, Holger A1 - Jikumaru, Yusuke A1 - Müller, Dörte A1 - Sicard, Adrien A1 - Leyser, Ottoline A1 - Yamaguchi, Shinjiro A1 - Lenhard, Michael T1 - SLOW MOTION is required for within-plant auxin homeostasis and normal timing of lateral organ initiation at the shoot meristem in Arabidopsis Y1 - 2010 SN - 1040-4651 ER - TY - JOUR A1 - Fujikura, Ushio A1 - Elsaesser, Lore A1 - Breuninger, Holger A1 - Sanchez-Rodriguez, Clara A1 - Ivakov, Alexander A1 - Laux, Thomas A1 - Findlay, Kim A1 - Persson, Staffan A1 - Lenhard, Michael T1 - Atkinesin-13A modulates cell-wall synthesis and cell expansion in arabidopsis thaliana via the THESEUS1 pathway JF - PLoS Genetics : a peer-reviewed, open-access journal N2 - Growth of plant organs relies on cell proliferation and expansion. While an increasingly detailed picture about the control of cell proliferation is emerging, our knowledge about the control of cell expansion remains more limited. We demonstrate the internal-motor kinesin AtKINESIN-13A (AtKIN13A) limits cell expansion and cell size in Arabidopsis thaliana, ion atkinl3a mutants forming larger petals with larger cells. The homolog, AtKINESIN-13B, also affects cell expansion and double mutants display growth, gametophytic and early embryonic defects, indicating a redundant role of he two genes. AtKIN13A is known to depolymerize microtubules and influence Golgi motility and distribution. Consistent his function, AtKIN13A interacts genetically with ANGUSTIFOLIA, encoding a regulator of Golgi dynamics. Reduced AtIGN13A activity alters cell wall structure as assessed by Fourier-transformed infrared-spectroscopy and triggers signalling he THESEUS1-dependent cell-wall integrity pathway, which in turn promotes the excess cell expansion in the atkinl3a mutant. Thus, our results indicate that the intracellular activity of AtKIN13A regulates cell expansion and wall architecture via THESEUS1, providing a compelling case of interplay between cell wall integrity sensing and expansion. Y1 - 2014 U6 - https://doi.org/10.1371/journal.pgen.1004627 SN - 1553-7390 SN - 1553-7404 VL - 10 IS - 9 PB - PLoS CY - San Fransisco ER - TY - JOUR A1 - Eriksson, Sven A1 - Stransfeld, Lena A1 - Adamski, Nikolai Maria A1 - Breuninger, Holger A1 - Lenhard, Michael T1 - KLUH/CYP78A5-dependent growth signaling coordinates floral organ growth in Arabidopsis Y1 - 2010 SN - 0960-9822 ER - TY - JOUR A1 - Cuong Nguyen Huu, A1 - Kappel, Christian A1 - Keller, Barbara A1 - Sicard, Adrien A1 - Takebayashi, Yumiko A1 - Breuninger, Holger A1 - Nowak, Michael D. A1 - Bäurle, Isabel A1 - Himmelbach, Axel A1 - Burkart, Michael A1 - Ebbing-Lohaus, Thomas A1 - Sakakibara, Hitoshi A1 - Altschmied, Lothar A1 - Conti, Elena A1 - Lenhard, Michael T1 - Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses JF - eLife N2 - Heterostyly is a wide-spread floral adaptation to promote outbreeding, yet its genetic basis and evolutionary origin remain poorly understood. In Primula (primroses), heterostyly is controlled by the S-locus supergene that determines the reciprocal arrangement of reproductive organs and incompatibility between the two morphs. However, the identities of the component genes remain unknown. Here, we identify the Primula CYP734A50 gene, encoding a putative brassinosteroid-degrading enzyme, as the G locus that determines the style-length dimorphism. CYP734A50 is only present on the short-styled S-morph haplotype, it is specifically expressed in S-morph styles, and its loss or inactivation leads to long styles. The gene arose by a duplication specific to the Primulaceae lineage and shows an accelerated rate of molecular evolution. Thus, our results provide a mechanistic explanation for the Primula style-length dimorphism and begin to shed light on the evolution of the S-locus as a prime model for a complex plant supergene. Y1 - 2016 U6 - https://doi.org/10.7554/eLife.17956 SN - 2050-084X VL - 5 PB - eLife Sciences Publications CY - Cambridge ER - TY - JOUR A1 - Breuninger, Holger A1 - Lenhard, Michael T1 - Control of tissue and organ growth in plants Y1 - 2010 SN - 0070-2153 ER - TY - JOUR A1 - Breuninger, Holger A1 - Lenhard, Michael T1 - Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements JF - BMC PLANT BIOLOGY N2 - Background: Much of the organismal variation we observe in nature is due to differences in organ size. The observation that even closely related species can show large, stably inherited differences in organ size indicates a strong genetic component to the control of organ size. Despite recent progress in identifying factors controlling organ growth in plants, our overall understanding of this process remains limited, partly because the individual factors have not yet been connected into larger regulatory pathways or networks. To begin addressing this aim, we have studied the upstream regulation of expression of BIG BROTHER (BB), a central growth-control gene in Arabidopsis thaliana that prevents overgrowth of organs. Final organ size and BB expression levels are tightly correlated, implying the need for precise control of its expression. BB expression mirrors proliferative activity, yet the gene functions to limit proliferation, suggesting that it acts in an incoherent feedforward loop downstream of growth activators to prevent over-proliferation. Results: To investigate the upstream regulation of BB we combined a promoter deletion analysis with a phylogenetic footprinting approach. We were able to narrow down important, highly conserved, cis-regulatory elements within the BB promoter. Promoter sequences of other Brassicaceae species were able to partially complement the A. thaliana bb-1 mutant, suggesting that at least within the Brassicaceae family the regulatory pathways are conserved. Conclusions: This work underlines the complexity involved in precise quantitative control of gene expression and lays the foundation for identifying important upstream regulators that determine BB expression levels and thus final organ size. Y1 - 2012 U6 - https://doi.org/10.1186/1471-2229-12-41 SN - 1471-2229 VL - 12 PB - BIOMED CENTRAL LTD CY - LONDON ER -