The induction and maintenance of flowering in Impatiens

Development ◽  
1997 ◽  
Vol 124 (17) ◽  
pp. 3343-3351 ◽  
Author(s):  
S. Pouteau ◽  
D. Nicholls ◽  
F. Tooke ◽  
E. Coen ◽  
N. Battey

The mechanisms that establish the floral meristem are now becoming clearer, but the way in which flowering is maintained is less well understood. Impatiens balsamina provides a unique opportunity to address this question because reversion to vegetative growth can be obtained in a predictable way by transferring plants from inductive to non-inductive conditions. Following increasing amounts of induction, reversion takes place at progressively later stages of flower development. Partial flower induction and defoliation experiments show that a floral signal is produced in the cotyledon in response to inductive conditions and that this signal progressively diminishes after transfer to non-inductive conditions, during reversion. Therefore reversion in Impatiens is most likely due to the failure of leaves to become permanent sources of inductive signal in addition to the lack of meristem commitment to flowering. Analysis of the expression of the Impatiens homologues of the meristem identity genes floricaula and squamosa indicates that a change in floricaula transcription is not associated with the establishment or maintenance of the floral meristem in this species. Squamosa transcription is associated with floral development and petal initiation, and is maintained in existing petal or petaloid primordia even after the meristem has reverted. However, it is not expressed in the reverted meristem, in which leaves are initiated in whorled phyllotaxis and without axillary meristems, both characteristics usually associated with the floral meristem. These observations show that squamosa expression is not needed for the maintenance of these floral characters. The requirement for the production of the floral signal in the leaf during the process of flower development may reflect an additional function separate to that of squamosa activation; alternatively the signal may be required to ensure continued transcriptional activation in the meristem.


1991 ◽  
Vol 69 (4) ◽  
pp. 844-857 ◽  
Author(s):  
Taylor A. Steeves ◽  
Margaret W. Steeves ◽  
A. Randall Olson

The development of the flower of Amelanchier alnifolia from initiation to the onset of anthesis is described. Sepals are formed sequentially, but interprimordial zonal growth results in the initiation of the hypanthium. Petals and stamens arise in whorls around the floral meristem as the hypanthium extends. They show neither coalescence nor adnation and do not appear to contribute to the development of the hypanthium. Gynoecial primordia arise individually, give rise to the styles and stigmas, and are joined basally by zonal growth to produce the roof of the ovary. The wall of the inferior ovary is interpreted as a gynoecial hypanthium. It is difficult to determine the extent to which the gynoecial primordia contribute to the development of the ovary. They do not give rise to most of its structure but may be responsible for the initiation of the ovules. There is evidence of postgenital fusion of the septal margins as they converge in the centre of the ovary. The timing of events in floral development is recorded for the locality of the study. The observations are discussed in relation to current theories concerning the nature of the inferior ovary. Key words: Amelanchier, flower, development, inferior ovary, hypanthium.



Author(s):  
Yun Hu ◽  
Li Wang ◽  
Ru Jia ◽  
Wanqi Liang ◽  
Xuelian Zhang ◽  
...  

Abstract Floral patterning is regulated by intricate networks of floral identity genes. The peculiar MADS32 subfamily genes, absent in eudicots but prevalent in monocots, regulate floral organ identity. However, how the MADS32 family genes interact with other floral homeotic genes during flower development is mostly unknown. We show here that the rice homeotic transcription factor OsMADS32 regulates floral patterning by interacting synergistically with E class protein OsMADS6 in a dosage-dependent manner. Furthermore, our results indicate important roles of OsMADS32 in defining stamen, pistil and ovule development through physical and genetic interactions with OsMADS1, OsMADS58 and OsMADS13, and in specifying floral meristem identity with OsMADS6, OsMADS3 and OsMADS58 respectively. Our findings suggest that OsMADS32 is an important factor for floral meristem identity maintenance and that it integrates the action of other MADS-box homeotic proteins to sustain floral organ specification and development in rice. Given that OsMADS32 is an orphan gene and absent in eudicots, our data substantially expand our understanding of flower development in plants.



Development ◽  
2002 ◽  
Vol 129 (9) ◽  
pp. 2079-2086 ◽  
Author(s):  
Rebecca S. Lamb ◽  
Theresa A. Hill ◽  
Queenie K.-G. Tan ◽  
Vivian F. Irish

The Arabidopsis APETALA3 (AP3) floral homeotic gene is required for specifying petal and stamen identities, and is expressed in a spatially limited domain of cells in the floral meristem that will give rise to these organs. Here we show that the floral meristem identity genes LEAFY (LFY) and APETALA1 (AP1) are required for the activation of AP3. The LFY transcription factor binds to a sequence, with dyad symmetry, that lies within a region of the AP3 promoter required for early expression of AP3. Mutation of this region abolishes LFY binding in vitro and in yeast one hybrid assays, but has no obvious effect on AP3 expression in planta. Experiments using a steroid-inducible form of LFY show that, in contrast to its direct transcriptional activation of other floral homeotic genes, LFY acts in both a direct and an indirect manner to regulate AP3 expression. This LFY-induced expression of AP3 depends in part on the function of the APETALA1 (AP1) floral homeotic gene, since mutations in AP1 reduce LFY-dependent induction of AP3 expression. LFY therefore appears to act through several pathways, one of which is dependent on AP1 activity, to regulate AP3 expression.



Development ◽  
1993 ◽  
Vol 119 (2) ◽  
pp. 397-418 ◽  
Author(s):  
S.E. Clark ◽  
M.P. Running ◽  
E.M. Meyerowitz

We have investigated the effects on plant development of mutations in the Arabidopsis thaliana CLAVATA1 gene. In clavata1 plants, vegetative, inflorescence and floral meristems are all enlarged relative to wild type. The apical meristem can fasciate in the more severe mutant alleles, and this fasciation can occur prior to the transition to flowering. Flowers of clavata1 plants can have increased numbers of organs in all four whorls, and can also have additional whorls not present in wild-type flowers. Double mutant combinations of clavata1 with agamous, apetala2, apetala3 and pistillata indicate that CLAVATA1 controls the underlying floral meristem structure upon which these homeotic genes act. Double mutant combinations of clavata1 with apetala1 and leafy indicate CLAVATA1 plays a role in establishing and maintaining floral meristem identity, in addition to its role in controlling meristem size. In support of this, RNA expression patterns of AGAMOUS and APETALA1 are altered in clavata1 flowers.



2021 ◽  
Vol 22 (10) ◽  
pp. 5221
Author(s):  
Danqi Zeng ◽  
Jaime A. Teixeira da Silva ◽  
Mingze Zhang ◽  
Zhenming Yu ◽  
Can Si ◽  
...  

The APETALA2 (AP2) transcription factors (TFs) play crucial roles in regulating development in plants. However, a comprehensive analysis of the AP2 family members in a valuable Chinese herbal orchid, Dendrobium officinale, or in other orchids, is limited. In this study, the 14 DoAP2 TFs that were identified from the D. officinale genome and named DoAP2-1 to DoAP2-14 were divided into three clades: euAP2, euANT, and basalANT. The promoters of all DoAP2 genes contained cis-regulatory elements related to plant development and also responsive to plant hormones and stress. qRT-PCR analysis showed the abundant expression of DoAP2-2, DoAP2-5, DoAP2-7, DoAP2-8 and DoAP2-12 genes in protocorm-like bodies (PLBs), while DoAP2-3, DoAP2-4, DoAP2-6, DoAP2-9, DoAP2-10 and DoAP2-11 expression was strong in plantlets. In addition, the expression of some DoAP2 genes was down-regulated during flower development. These results suggest that DoAP2 genes may play roles in plant regeneration and flower development in D. officinale. Four DoAP2 genes (DoAP2-1 from euAP2, DoAP2-2 from euANT, and DoAP2-6 and DoAP2-11 from basal ANT) were selected for further analyses. The transcriptional activation of DoAP2-1, DoAP2-2, DoAP2-6 and DoAP2-11 proteins, which were localized in the nucleus of Arabidopsis thaliana mesophyll protoplasts, was further analyzed by a dual-luciferase reporter gene system in Nicotiana benthamiana leaves. Our data showed that pBD-DoAP2-1, pBD-DoAP2-2, pBD-DoAP2-6 and pBD-DoAP2-11 significantly repressed the expression of the LUC reporter compared with the negative control (pBD), suggesting that these DoAP2 proteins may act as transcriptional repressors in the nucleus of plant cells. Our findings on AP2 genes in D. officinale shed light on the function of AP2 genes in this orchid and other plant species.



1973 ◽  
Vol 51 (3) ◽  
pp. 647-656 ◽  
Author(s):  
U. Posluszny ◽  
R. Sattler

The floral appendages of Potamogeton densus are initiated in an acropetal sequence. The first primordia to be seen externally are those of the lateral tepals, though sectioning young floral buds (longitudinally, parallel to the inflorescence axis) reveals initial activity in the region of the lower median (abaxial) tepal and stamen at a time when the floral meristem is not yet clearly demarcated. The lateral (transversal) stamens are initiated simultaneously and unlike the median stamens each arises as two separate primordia. The upper median (adaxial) tepal and stamen develop late in relation to the other floral appendages, and in some specimens are completely absent. Rates of growth of the primordia vary greatly. Though the lower median tepal and stamen are initiated first, they grow slowly up to gynoecial inception, while the upper median tepal appears late in the developmental sequence but grows rapidly, soon overtaking the other tepal primordia. The four gynoecial primordia arise almost simultaneously, although variation in their sequence of inception occurs. The two-layered tunica of the floral apices gives rise to all floral appendages through periclinal divisions in the second layer. The third layer (corpus) is involved as well in the initiation of the stamen primordia. Procambial strands develop acropetally, lagging behind primordial initiation. The lateral stamens though initiating as two primordia each form a single, central procambial strand, which differentiates after growth between the two primordia of the thecae has occurred. A great amount of deviation from the normal tetramerous flower is found, including completely trimerous flowers, trimerous gynoecia with tetramerous perianth and androecium, and organs differentiating partially as tepals and partially as stamens.



2020 ◽  
Author(s):  
Liling Yang ◽  
Shilian Qi ◽  
Arfa touqeer ◽  
Haiyang Li ◽  
Xiaolan Zhang ◽  
...  

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.



2007 ◽  
Vol 104 (15) ◽  
pp. 6484-6489 ◽  
Author(s):  
P. Achard ◽  
M. Baghour ◽  
A. Chapple ◽  
P. Hedden ◽  
D. Van Der Straeten ◽  
...  


Sign in / Sign up

Export Citation Format

Share Document