scholarly journals The gene FLORAL ORGAN NUMBER1 regulates floral meristem size in rice and encodes a leucine-rich repeat receptor kinase orthologous to Arabidopsis CLAVATA1

Development ◽  
2004 ◽  
Vol 131 (22) ◽  
pp. 5649-5657 ◽  
Author(s):  
T. Suzaki
Keyword(s):  
Floral Organ ◽  
Floral Meristem ◽  
Receptor Kinase ◽  
Leucine Rich Repeat ◽  
Meristem Size

scholarly journals The ERECTA receptor kinase regulates Arabidopsis shoot apical meristem size, phyllotaxy and floral meristem identity

Development ◽  
2014 ◽  
Vol 141 (4) ◽  
pp. 830-841 ◽  
Author(s):  
T. Mandel ◽  
F. Moreau ◽  
Y. Kutsher ◽  
J. C. Fletcher ◽  
C. C. Carles ◽  
...  
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Floral Meristem ◽  
Receptor Kinase ◽  
Floral Meristem Identity ◽  
Meristem Size ◽  
Meristem Identity

scholarly journals The CLAVATA1Gene Encodes a Putative Receptor Kinase That Controls Shoot and Floral Meristem Size in Arabidopsis

Cell ◽  
1997 ◽  
Vol 89 (4) ◽  
pp. 575-585 ◽  
Author(s):  
Steven E Clark ◽  
Robert W Williams ◽  
Elliot M Meyerowitz
Keyword(s):  
Floral Meristem ◽  
Receptor Kinase ◽  
Meristem Size ◽  
Putative Receptor

scholarly journals Identification and characterization of regulatory pathways involved in early flowering in the new leaves of alfalfa (Medicago sativa L.) by transcriptome analysis

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Dongmei Ma ◽  
Bei Liu ◽  
Lingqiao Ge ◽  
Yinyin Weng ◽  
Xiaohui Cao ◽  
...  
Keyword(s):  
Medicago Sativa ◽  
Secondary Metabolism ◽  
Flowering Time ◽  
Degradation Pathway ◽  
Early Flowering ◽  
Receptor Kinase ◽  
Leucine Rich Repeat ◽  
Kinase Family ◽  
Pathogenesis Related ◽  
Early Flowering Phenotype

Abstract Background Alfalfa (Medicago sativa L.) is a perennial legume extensively planted throughout the world as a high nutritive value livestock forage. Flowering time is an important agronomic trait that contributes to the production of alfalfa hay and seeds. However, the underlying molecular mechanisms of flowering time regulation in alfalfa are not well understood. Results In this study, an early-flowering alfalfa genotype 80 and a late-flowering alfalfa genotype 195 were characterized for the flowering phenotype. Our analysis revealed that the lower jasmonate (JA) content in new leaves and the downregulation of JA biosynthetic genes (i.e. lipoxygenase, the 12-oxophytodienoate reductase-like protein, and salicylic acid carboxyl methyltransferase) may play essential roles in the early-flowering phenotype of genotype 80. Further research indicated that genes encode pathogenesis-related proteins [e.g. leucine rich repeat (LRR) family proteins, receptor-like proteins, and toll-interleukin-like receptor (TIR)-nucleotide-binding site (NBS)-LRR class proteins] and members of the signaling receptor kinase family [LRR proteins, kinases domain of unknown function 26 (DUF26) and wheat leucine-rich repeat receptor-like kinase10 (LRK10)-like kinases] are related to early flowering in alfalfa. Additionally, those involved in secondary metabolism (2-oxoglutarate/Fe (II)-dependent dioxygenases and UDP-glycosyltransferase) and the proteasome degradation pathway [really interesting new gene (RING)/U-box superfamily proteins and F-box family proteins] are also related to early flowering in alfalfa. Conclusions Integrated phenotypical, physiological, and transcriptomic analyses demonstrate that hormone biosynthesis and signaling pathways, pathogenesis-related genes, signaling receptor kinase family genes, secondary metabolism genes, and proteasome degradation pathway genes are responsible for the early flowering phenotype in alfalfa. This will provide new insights into future studies of flowering time in alfalfa and inform genetic improvement strategies for optimizing this important trait.

scholarly journals SlGT11 Controls Floral Organ Patterning and Floral Determinacy in Tomato

2020 ◽  
Author(s):  
Liling Yang ◽  
Shilian Qi ◽  
Arfa touqeer ◽  
Haiyang Li ◽  
Xiaolan Zhang ◽  
...  
Keyword(s):  
Floral Development ◽  
Bulked Segregant Analysis ◽  
Floral Organ ◽  
Fruit Production ◽  
Floral Meristem ◽  
Rnai Silencing ◽  
The Third ◽  
Spatiotemporal Expression ◽  
Higher Temperature ◽  
Floral Determinacy

Abstract 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.Results: Here, we analyzed a novel tomato stamenless like flower (slf) mutant in which the development of stamens and carpels is disturbed, with carpelloid structure formed in the third whorl and ectopic formation of floral and shoot apical meristem in the fourth whorl. Using bulked segregant analysis (BSA), we assigned the causal mutation to the gene Solanum lycopersicum GT11 (SlGT11) that encodes a transcription factor belonging to Trihelix gene family. SlGT11 is expressed in the early stages of the flower and the expression becomes more specific to the primordium position corresponding to stamens and carpels in later stages of the floral development. Further RNAi silencing of SlGT11 verifies the defective phenotypes of the slf mutant. The carpelloid stamen in slf mutant indicates that SlGT11 is required for B-function activity in the third whorl. The failed termination of floral meristem and the occurrence of floral reversion in slf indicate that part of the C-function requires SlGT11 activity in the fourth whorl. Furthermore, we find that at higher temperature, the defects of slf mutant are substantially enhanced, with petals transformed into sepals, all stamens disappeared, and the frequency of ectopic shoot/floral meristem in fourth whorl increased, indicating that SlGT11 functions in the development of the three inner floral whorls. Consistent with the observed phenotypes, it was found that B, C and an E-type MADS-box genes were in part down regulated in slf mutants.Conclusions: Together with the spatiotemporal expression pattern, we suggest that SlGT11 functions in floral organ patterning and maintenance of floral determinacy in tomato.

The ULTRAPETALA gene controls shoot and floral meristem size in Arabidopsis

Development ◽  
2001 ◽  
Vol 128 (8) ◽  
pp. 1323-1333 ◽  
Author(s):  
J.C. Fletcher
Keyword(s):  
Signal Transduction Pathway ◽  
Floral Meristem ◽  
Transduction Pathway ◽  
Wild Type ◽  
Inflorescence Meristem ◽  
Genetic Studies ◽  
Meristem Cell ◽  
Meristem Size ◽  
Cell Accumulation ◽  
Floral Meristems

The regulation of proper shoot and floral meristem size during plant development is mediated by a complex interaction of stem cell promoting and restricting factors. The phenotypic effects of mutations in the ULTRAPETALA gene, which is required to control shoot and floral meristem cell accumulation in Arabidopsis thaliana, are described. ultrapetala flowers contain more floral organs and whorls than wild-type plants, phenotypes that correlate with an increase in floral meristem size preceding organ initiation. ultrapetala plants also produce more floral meristems than wild-type plants, correlating with an increase in inflorescence meristem size without visible fasciation. Expression analysis indicates that ULTRAPETALA controls meristem cell accumulation partly by limiting the domain of CLAVATA1 expression. Genetic studies show that ULTRAPETALA acts independently of ERA1, but has overlapping functions with PERIANTHIA and the CLAVATA signal transduction pathway in controlling shoot and floral meristem size and meristem determinacy. Thus ULTRAPETALA defines a novel locus that restricts meristem cell accumulation in Arabidopsis shoot and floral meristems.

scholarly journals Genetic architecture underlying variation in floral meristem termination in Aquilegia

2021 ◽  
Author(s):  
Ya Min ◽  
Evangeline S. Ballerini ◽  
Molly B. Edwards ◽  
Scott A. Hodges ◽  
Elena M. Kramer
Keyword(s):  
Candidate Genes ◽  
Genetic Architecture ◽  
Expression Patterns ◽  
Cell Activity ◽  
Morphological Diversity ◽  
Floral Organ ◽  
Floral Meristem ◽  
Potential Candidate ◽  
Evolutionary Level ◽  
Trait Locus

Floral organs are produced by floral meristems (FMs), which harbor stem cells in their centers. Since each flower only has a finite number of organs, the stem cell activity of a FM will always terminate at a specific time point, a process termed floral meristem termination (FMT). Variation in the timing of FMT can give rise to floral morphological diversity, but how this process is fine-tuned at a developmental and evolutionary level is poorly understood. Flowers from the genus Aquilegia share identical floral organ arrangement except for stamen whorl numbers (SWN), making Aquilegia a well-suited system for investigation of this process: differences in SWN between species represent differences in the timing of FMT. By crossing A. canadensis and A. brevistyla, quantitative trait locus (QTL) mapping has revealed a complex genetic architecture with seven QTL. We identified potential candidate genes under each QTL and characterized novel expression patterns of select candidate genes using in situ hybridization. To our knowledge, this is the first attempt to dissect the genetic basis of how natural variation in the timing of FMT is regulated and our results provide insight into how floral morphological diversity can be generated at the meristematic level.

scholarly journals Mechanistic analysis of the SERK3 elongated allele defines a role for BIR ectodomains in brassinosteroid signaling

2018 ◽  
Author(s):  
Ulrich Hohmann ◽  
Joël Nicolet ◽  
Andrea Moretti ◽  
Ludwig A. Hothorn ◽  
Michael Hothorn
Keyword(s):  
Receptor Activation ◽  
Surface Patch ◽  
Receptor Kinase ◽  
Leucine Rich Repeat ◽  
Negative Regulators ◽  
Signaling Complex ◽  
The Core ◽  
Mechanistic Analysis ◽  
Brassinosteroid Signaling

AbstractThe leucine-rich repeat receptor kinase (LRR-RK) BRI1 requires a shape-complementary SERK co-receptor for brassinosteroid sensing and receptor activation. Interface mutations that weaken the interaction between receptor and co-receptor in vitro reduce brassinosteroid signaling responses. The SERK3 elongated (elg) allele maps to the complex interface and shows enhanced brassinosteroid signaling, but surprisingly no tighter binding to the BRI1 ectodomain in vitro. Here, we report that rather than promoting the interaction with BRI1, the elg mutation disrupts the ability of the co-receptor to interact with the ectodomains of BIR receptor pseudokinases, negative regulators of LRR-RK signaling. A conserved lateral surface patch in BIR LRR domains is required for targeting SERK co-receptors and the elg allele maps to the core of the complex interface in a 1.25 Å BIR3 - SERK1 structure. Collectively, our structural, quantitative biochemical and genetic analyses suggest that brassinosteroid signaling complex formation is negatively regulated by BIR receptor ectodomains.

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