By Jean-Claude Kader, Michel Delseny
Edited through Jean-Claude Kader and Michel Delseny and supported through a world Editorial Board, Advances in Botanical learn publishes in-depth and updated studies on a variety of issues in plant sciences. at present in its fiftieth quantity, the sequence contains a wide variety of experiences by way of well-known specialists on all features of plant genetics, biochemistry, mobile biology, molecular biology, body structure and ecology. This eclectic quantity positive aspects six studies on state-of-the-art themes of curiosity to postgraduates and researchers alike. * Multidisciplinary reports written from a large diversity of clinical views * For over 30 years, sequence has loved a name for excellence * individuals the world over well-known experts of their respective fields
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Extra info for Advances in Botanical Research, Vol. 55
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.
2009) suggest that a gradient of these small RNAs is formed, which could define the expression boundary of their targets ARF3 and ARF4. A signalling molecule often used for positional information is auxin, and Pekker et al. (2005) have suggested that auxin could act as an abaxially polarising signal, activating ARF3 and ARF4. , 2003). E. LEAF DEVELOPMENT Leaf development proceeds through various different steps during which cell proliferation, cell expansion and cell differentiation occur. One major question is: how is this process coordinated?
C. FERRA strobilus, resulting in the production of female structures at the apex (Fig. 1B). , 2002), postulates a sex-determining role for B-sister MADS box genes, whose expression is proposed to have moved acropetally in a female strobilus to leave male structures in basal positions (Fig. 1C). In general, therefore, the OOM and OOF hypotheses focus below the level of LFY and NLY in the hierarchical control of gene expression, and postulate a spatial change in MADS box gene expression to form a boundary of B- or B-sister expression in a previously unisexual strobilus, thereby making this bisexual.
Advances in Botanical Research, Vol. 55 by Jean-Claude Kader, Michel Delseny
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