@article{EldridgeLangowskiStaceyetal.2016,
  author    = {Eldridge, Tilly and Langowski, Lukasz and Stacey, Nicola and Jantzen, Friederike and Moubayidin, Laila and Sicard, Adrien and Southam, Paul and Kennaway, Richard and Lenhard, Michael and Coen, Enrico S. and Ostergaard, Lars},
  title     = {Fruit shape diversity in the Brassicaceae is generated by varying patterns of anisotropy},
  series = {Development : Company of Biologists},
  volume    = {143},
  journal   = {Development : Company of Biologists},
  publisher = {Company of Biologists Limited},
  address   = {Cambridge},
  issn      = {0950-1991},
  doi       = {10.1242/dev.135327},
  pages     = {3394 -- 3406},
  year      = {2016},
  abstract  = {Fruits exhibit a vast array of different 3D shapes, from simple spheres and cylinders to more complex curved forms; however, the mechanism by which growth is oriented and coordinated to generate this diversity of forms is unclear. Here, we compare the growth patterns and orientations for two very different fruit shapes in the Brassicaceae: the heart-shaped Capsella rubella silicle and the near-cylindrical Arabidopsis thaliana silique. We show, through a combination of clonal and morphological analyses, that the different shapes involve different patterns of anisotropic growth during three phases. These experimental data can be accounted for by a tissue level model in which specified growth rates vary in space and time and are oriented by a proximodistal polarity field. The resulting tissue conflicts lead to deformation of the tissue as it grows. The model allows us to identify tissue-specific and temporally specific activities required to obtain the individual shapes. One such activity may be provided by the valve-identity gene FRUITFULL, which we show through comparative mutant analysis to modulate fruit shape during post-fertilisation growth of both species. Simple modulations of the model presented here can also broadly account for the variety of shapes in other Brassicaceae species, thus providing a simplified framework for fruit development and shape diversity.},
  language  = {en}
}
@article{SicardStaceyHermannetal.2011,
  author    = {Sicard, Adrien and Stacey, Nicola and Hermann, Katrin and Dessoly, Jimmy and Neuffer, Barbara and B{\"a}urle, Isabel and Lenhard, Michael},
  title     = {Genetics, evolution, and adaptive significance of the selfing syndrome in the genus Capsella},
  series = {The plant cell},
  volume    = {23},
  journal   = {The plant cell},
  number    = {9},
  publisher = {American Society of Plant Physiologists},
  address   = {Rockville},
  issn      = {1040-4651},
  doi       = {10.1105/tpc.111.088237},
  pages     = {3156 -- 3171},
  year      = {2011},
  abstract  = {The change from outbreeding to selfing is one of the most frequent evolutionary transitions in flowering plants. It is often accompanied by characteristic morphological and functional changes to the flowers (the selfing syndrome), including reduced flower size and opening. Little is known about the developmental and genetic basis of the selfing syndrome, as well as its adaptive significance. Here, we address these issues using the two closely related species Capsella grandiflora (the ancestral outbreeder) and red shepherd's purse (Capsella rubella, the derived selfer). In C. rubella, petal size has been decreased by shortening the period of proliferative growth. Using interspecific recombinant inbred lines, we show that differences in petal size and flower opening between the two species each have a complex genetic basis involving allelic differences at multiple loci. An intraspecific cross within C. rubella suggests that flower size and opening have been decreased in the C. rubella lineage before its extensive geographical spread. Lastly, by generating plants that likely resemble the earliest ancestors of the C. rubella lineage, we provide evidence that evolution of the selfing syndrome was at least partly driven by selection for efficient self-pollination. Thus, our studies pave the way for a molecular dissection of selfing-syndrome evolution.},
  language  = {en}
}
@article{DongJantzenStaceyetal.2019,
  author    = {Dong, Yang and Jantzen, Friederike and Stacey, Nicola and Langowski, Lukasz and Moubayidin, Laila and Simura, Jan and Ljung, Karin and Ostergaard, Lars},
  title     = {Regulatory Diversification of INDEHISCENT in the Capsella Genus Directs Variation in Fruit Morphology},
  series = {Current biology},
  volume    = {29},
  journal   = {Current biology},
  number    = {6},
  publisher = {Cell Press},
  address   = {Cambridge},
  issn      = {0960-9822},
  doi       = {10.1016/j.cub.2019.01.057},
  pages     = {1038 -- 1046},
  year      = {2019},
  abstract  = {Evolution of gene-regulatory sequences is considered the primary driver of morphological variation [1-3]. In animals, the diversity of body plans between distantly related phyla is due to the differential expression patterns of conserved "toolkit' genes [4]. In plants, variation in expression domains similarly underlie most of the reported diversity of organ shape both in natural evolution and in the domestication of crops [5-9]. The heart-shaped fruit from members of the Capsella genus is a morphological novelty that has evolved after Capsella diverged from Arabidopsis similar to 8 mya [10]. Comparative studies of fruit growth in Capsella and Arabidopsis revealed that the difference in shape is caused by local control of anisotropic growth [11]. Here, we show that sequence variation in regulatory domains of the fruit-tissue identity gene, INDEHISCENT (IND), is responsible for expansion of its expression domain in the heart-shaped fruits from Capsella rubella. We demonstrate that expression of this CrIND gene in the apical part of the valves in Capsella contributes to the heart-shaped appearance. While studies on morphological diversity have revealed the importance of cis-regulatory sequence evolution, few examples exist where the downstream effects of such variation have been characterized in detail. We describe here how CrIND exerts its function on Capsella fruit shape by binding sequence elements of auxin biosynthesis genes to activate their expression and ensure auxin accumulation into highly localized maxima in the fruit valves. Thus, our data provide a direct link between changes in expression pattern and altered hormone homeostasis in the evolution of morphological novelty.},
  language  = {en}
}
@article{LohmannStaceyBreuningeretal.2010,
  author    = {Lohmann, Daniel and Stacey, Nicola and Breuninger, Holger and Jikumaru, Yusuke and M{\"u}ller, D{\"o}rte and Sicard, Adrien and Leyser, Ottoline and Yamaguchi, Shinjiro and Lenhard, Michael},
  title     = {SLOW MOTION is required for within-plant auxin homeostasis and normal timing of lateral organ initiation at the shoot meristem in Arabidopsis},
  issn      = {1040-4651},
  year      = {2010},
  language  = {en}
}