By Jean-Claude Kader, Michel Delseny
Edited through Jean-Claude Kader and Michel Delseny and supported by means of a global Editorial Board, Advances in Botanical examine publishes in-depth and up to date stories on quite a lot of subject matters in plant sciences. presently in its fiftieth quantity, the sequence encompasses a wide variety of studies by means of famous specialists on all elements of plant genetics, biochemistry, telephone biology, molecular biology, body structure and ecology. This eclectic quantity beneficial properties six reports on state-of-the-art subject matters of curiosity to postgraduates and researchers alike. * Multidisciplinary studies written from a extensive diversity of clinical views * For over 30 years, sequence has loved a name for excellence * members across the world famous experts of their respective fields
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Additional info for Advances in Botanical Research, Vol. 55
2010). , 2010). The process of leaf serration shows many similarities to that of leaflet formation in dissected leaves. For example, leaf dissection in Cardamine hirsuta also relies on the activity of CUC boundary-specifying genes in the area delimiting leaflet primordia and on the activity of KNOX genes at the leaflet initiation position, which cause a delay in cell differentiation relative to cell proliferation. , 2006). Interestingly, these modulations of leaf margins clearly provide evidence that processes related to meristem function are also used during lateral organ development.
7). In accordance with this model, the regulators Auxin gradient Gynoecium primordia Mature Gynoecium Fruit Fertilisation ind. dev. switch Fig. 7. Apical–basal patterning in the Arabidopsis gynoecium. An apical–basal auxin gradient has been suggested to participate in the apical–basal patterning of the gyneocium by positioning the borders between the apical style and stigma, the centrally placed ovary, and the short stem or gynophores at the base. After fertilisation, the ovary continues to elongate.
Based on genetic analyses, Dinneny et al. (2005) proposed a model in which the cooperative activity of FIL, YAB3 and JAG would activate the transcription of FUL and SHP genes in the valves and valve margins, respectively. According to this model, a high level of FIL/YAB/JAG activity would turn on FUL expression in the valves, while the activation of SHP in the valve margins would require a weaker activity of this same module. This model fits nicely with the observed phenotypes, but whether the activation of FUL and SHP lies in differences in YAB/JAG levels in different domains or in some other type of molecular interaction remains to be seen.
Advances in Botanical Research, Vol. 55 by Jean-Claude Kader, Michel Delseny