SlGT11 controls floral organ patterning and floral determinacy in tomato [PDF]
Background Flower development directly affects fruit production in tomato. Despite the framework mediated by ABC genes have been established in Arabidopsis, the spatiotemporal precision of floral development in tomato has not been well examined.
Liling Yang +6 more
doaj +2 more sources
Genetic and Molecular Control of Floral Organ Identity in Cereals [PDF]
Grasses represent a major family of monocots comprising mostly cereals. When compared to their eudicot counterparts, cereals show a remarkable morphological diversity.
Gyuhwa Chung +2 more
exaly +3 more sources
A Developmental Basis for Stochasticity in Floral Organ Numbers [PDF]
Stochasticity ubiquitously inevitably appears at all levels from molecular traits to multicellular, morphological traits. Intrinsic stochasticity in biochemical reactions underlies the typical intercellular distributions of chemical concentrations, e.g.,
Miho S Kitazawa, Koichi eFujimoto
doaj +2 more sources
Floral organ development goes live [PDF]
Lea Rambaud-Lavigne +2 more
exaly +2 more sources
AGAMOUS mediates timing of guard cell formation during gynoecium development.
In Arabidopsis thaliana, stomata are composed of two guard cells that control the aperture of a central pore to facilitate gas exchange between the plant and its environment, which is particularly important during photosynthesis.
Ailbhe J Brazel +6 more
doaj +1 more source
The effect of molecular, morphological and spectral reflectance evolution on nicotiana polyploids of different ages [PDF]
PhDInterspecific hybridisation accompanied by multiplication of chromosome number, or allopolyploidy, results in rapid genetic, epigenetic, chromosomal and morphological changes.
McCarthy, Elizabeth Wetzel
core +4 more sources
Linking Hsp90 function to micro-environmental and stochastic variation in floralorgans of Iris pumila L. [PDF]
Hsp90 is an environmentally responsive molecular chaperone that was found to play a key role in buffering against genetic and non-genetic perturbations in the model organisms Arabidopsis and Drosophila.
Tucić Branka +3 more
doaj +1 more source
Histone acetylation accompanied with promoter sequences displaying differential expression profiles of B-class MADS-box genes for phalaenopsis floral morphogenesis. [PDF]
Five B-class MADS-box genes, including four APETALA3 (AP3)-like PeMADS2∼5 and one PISTILLATA (PI)-like PeMADS6, specify the spectacular flower morphology in orchids. The PI-like PeMADS6 ubiquitously expresses in all floral organs. The four AP3-like genes,
Chia-Chi Hsu +8 more
doaj +1 more source
Quantitative Live Confocal Imaging in Aquilegia Floral Meristems
In this study, we present a detailed protocol for live imaging and quantitative analysis of floral meristem development in Aquilegia coerulea, a member of the buttercup family (Ranunculaceae).
Ya Min, Stephanie Conway, Elena Kramer
doaj +1 more source
In planta localisation patterns of MADS domain proteins during floral development in Arabidopsis thaliana [PDF]
Background: MADS domain transcription factors play important roles in various developmental processes in flowering plants. Members of this family play a prominent role in the transition to flowering and the specification of floral organ identity. Several
Angenent, G.C. +6 more
core +1 more source

