Role of gibberellins in the development of floral organs of the gibberellin-deficient mutant, ga1-1, of Arabidopsis thaliana

1999 ◽  
Vol 77 (7) ◽  
pp. 944-954 ◽  
Author(s):  
Nobuharu Goto ◽  
Richard P Pharis

The gibberellin-deficient mutant, ga1-1 (NG5) of Arabidopsis thaliana, when induced by 16-h-long days, will form floral buds. However, the flower stalk is very short and floral organs within the flowers remain undeveloped; petal growth is arrested, with the petals being scaly and translucent, the stamens are abortive, the filaments do not elongate, and the pollen does not mature. Sepals and pistils are also underdeveloped. All of the above defects of this mutant can be completely eliminated if certain gibberellins (GAs) are applied to the young floral buds. That is, the applied GA acts to normalize not only plant height but also development of floral organs, thereby yielding good seed set from self-pollination. There were appreciable differences in the efficacy of different GA structures in normalizing the various floral organs. For seed production, the order of efficacy was 2,2-dimethyl GA4 > GA7 > GA3 = GA4 > GA1 > GA5 = GA9. When 2,2-dimethyl GA4 was used to determine an optimal GA dose, the following pattern emerged: filament elongation and pollen development, 1-10 ng; petal and pistil growth, 1 ng; sepal growth, 0.1 ng; papilla elongation, 0.01 ng. However, one application at these doses was insufficient to normalize the flowers, which were formed one after another, and a continuing supply of GA at the optimal dose was required for normal flower development and seed set. We conclude from this work that GAs play an essential role in the development of floral organs of Arabidopsis and that petals and stamens (filaments and pollen) in particular develop normally only when GAs are present at the optimal level.Key words: Arabidopsis thaliana, floral organ development, gibberellin, gibberellin-deficient mutant, petal and pollen development, reproductive function.

2015 ◽  
Vol 90 (3) ◽  
pp. 163-174
Author(s):  
Hiroaki Kato ◽  
Yoshibumi Komeda ◽  
Tamao Saito ◽  
Hidetaka Ito ◽  
Atsushi Kato

Development ◽  
1997 ◽  
Vol 124 (13) ◽  
pp. 2645-2657 ◽  
Author(s):  
M. Spielman ◽  
D. Preuss ◽  
F.L. Li ◽  
W.E. Browne ◽  
R.J. Scott ◽  
...  

In flowering plants, male meiosis occurs in the microsporocyte to produce four microspores, each of which develops into a pollen grain. Here we describe four mutant alleles of TETRASPORE (TES), a gene essential for microsporocyte cytokinesis in Arabidopsis thaliana. Following failure of male meiotic cytokinesis in tes mutants, all four microspore nuclei remain within the same cytoplasm, with some completing their developmental programmes to form functional pollen nuclei. Both of the mitotic divisions seen in normal pollen development take place in tes mutants, including the asymmetric division required for the differentiation of gametes; some tes grains perform multiple asymmetric divisions in the same cytoplasm. tes pollen shows a variety of abnormalities subsequent to the cytokinetic defect, including fusion of nuclei, formation of ectopic internal walls, and disruptions to external wall patterning. In addition, ovules fertilized by tes pollen often abort, possibly because of excess paternal genomes in the endosperm. Thus tes mutants not only reveal a gene specific to male meiosis, but aid investigation of a wide range of processes in pollen development and function.


PLoS ONE ◽  
2009 ◽  
Vol 4 (3) ◽  
pp. e4780 ◽  
Author(s):  
Andi Gusti ◽  
Nicolas Baumberger ◽  
Moritz Nowack ◽  
Stefan Pusch ◽  
Herfried Eisler ◽  
...  

2020 ◽  
Author(s):  
Chunling Zhang ◽  
Yalin Sun ◽  
Ludan Wei ◽  
Wenjing Wang ◽  
Hang Li ◽  
...  

Abstract Background: Members of AP1/FUL subfamily genes play an essential role in the regulation of floral meristem transition, floral organ identity, and fruit ripping. At present, there have been insufficient studies to explain the function of the AP1/FUL-like subfamily genes in Asteraceae. Results: Here, we cloned two euAP1 clade genes TeAP1-1 and TeAP1-2, and three euFUL clade genes TeFUL1, TeFUL2, and TeFUL3 from marigold (Tagetes erecta). Expression profile analysis demonstrated that TeAP1-1 and TeAP1-2 were mainly expressed in receptacles, sepals, petals, and ovules. TeFUL1 and TeFUL3 were expressed in floral buds, stems and leaves as well as in productive tissues, while TeFUL2 was mainly expressed in floral buds and vegetative tissues. Transgenic Arabidopsis lines showed that overexpression TeAP1-2 or TeFUL2 resulted in early flowering, implying that these two genes might regulate the floral transition. Yeast two-hybrid analysis indicated that TeAP1/FUL proteins only interacted with TeSEP proteins to form heterodimers, and that TeFUL2 could also form a homodimer.Conclusion: In general, TeAP1-1 and TeAP1-2 might play a conserved role in regulating sepal and petal identity, just like the role of MADS-box class A genes, while TeFUL genes might display divergent functions. This study provides an insight into molecular mechanism of AP1/FUL-like genes in Asteraceae species.


Plants ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1767
Author(s):  
Annemarie Heiduk ◽  
Dewi Pramanik ◽  
Marlies Spaans ◽  
Loes Gast ◽  
Nemi Dorst ◽  
...  

Deceptive Ceropegia pitfall flowers are an outstanding example of synorganized morphological complexity. Floral organs functionally synergise to trap fly-pollinators inside the fused corolla. Successful pollination requires precise positioning of flies headfirst into cavities at the gynostegium. These cavities are formed by the corona, a specialized organ of corolline and/or staminal origin. The interplay of floral organs to achieve pollination is well studied but their evolutionary origin is still unclear. We aimed to obtain more insight in the homology of the corona and therefore investigated floral anatomy, ontogeny, vascularization, and differential MADS-box gene expression in Ceropegia sandersonii using X-ray microtomography, Light and Scanning Electronic Microscopy, and RT-PCR. During 10 defined developmental phases, the corona appears in phase 7 at the base of the stamens and was not found to be vascularized. A floral reference transcriptome was generated and 14 MADS-box gene homologs, representing all major MADS-box gene classes, were identified. B- and C-class gene expression was found in mature coronas. Our results indicate staminal origin of the corona, and we propose a first ABCDE-model for floral organ identity in Ceropegia to lay the foundation for a better understanding of the molecular background of pitfall flower evolution in Apocynaceae.


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