By Jean-Claude Kader, Michel Delseny
Edited via Jean-Claude Kader and Michel Delseny and supported via a world Editorial Board, Advances in Botanical examine publishes in-depth and up to date stories on quite a lot of themes in plant sciences. at present in its fiftieth quantity, the sequence contains a wide selection of reports via well-known specialists on all points of plant genetics, biochemistry, mobile biology, molecular biology, body structure and ecology. This eclectic quantity gains six studies on state of the art themes of curiosity to postgraduates and researchers alike. * Multidisciplinary studies written from a large diversity of clinical views * For over 30 years, sequence has loved a name for excellence * participants the world over famous professionals of their respective fields
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Extra resources for Advances in Botanical Research, Vol. 55
This disruption of stem cell maintenance makes the flower determinate and assures its future fertility by blocking the development of floral organs, in the place of ovules, within the gynoecium. A. AGAMOUS (AG), THE MAIN GENE RESPONSIBLE FOR CARPEL DEVELOPMENT, ALSO PLAYS A CENTRAL ROLE IN FLORAL MERISTEM TERMINATION AG function is not restricted to the control of stamen and carpel identity. It also promotes floral meristem termination (Fig. , 1990). Stem cells are thus indefinitely maintained within the FM and allow for the endless production of floral organs.
FERRA specific origin by duplication in the angiosperms, also casting some doubt on the idea that the genes responsible for the E-function arose specifically with the angiosperms. , 2010). III. THE BASIC DEVELOPMENTAL PLAN OF LATERAL ORGANS A. LEAVES AND CARPELS SHARE BASIC REGULATORY PATHWAYS As mentioned in the previous section, leaves and floral organs most likely have a common evolutionary origin, or as Goethe memorably put it: Alles ist Blatt (All is Leaf; von Goethe, 1790). An increasing amount of evidence suggests that the pathways regulating the basic morphological outline of ancestral leaf-like organs have been recruited to the developmental programmes of both leaves and floral organs, including the carpels, of presentday plants, although in the latter case, these have been slightly modified and positioned downstream of genes determining floral organ identity.
2000; Theissen and Saedler, 2001). Theissen and Melzer (2007) discuss the possibility that, before the flower, dimers of C-function genes may have specified the development of female reproductive organs, and that the evolution of quaternary MADS box complexes, incorporating both C- and E-function proteins, may have built on this mechanism to generate the carpel. More precisely, the evolution of MADS box quaternary complexes is hypothesised to have caused transcription factor binding to two distinct MADS box binding motifs, termed CArG boxes, in the cis-acting control regions of their target genes.