scholarly journals A soybean MADS-box protein modulates floral organ numbers, petal identity and sterility

2014 ◽  
Vol 14 (1) ◽  
pp. 89 ◽  
Author(s):  
Fang Huang ◽  
Guangli Xu ◽  
Yingjun Chi ◽  
Haicui Liu ◽  
Qian Xue ◽  
...  
Keyword(s):  
Floral Organ ◽  
Mads Box ◽  
Petal Identity

scholarly journals Functional conservation and divergence of five AP1/FUL-like genes in Marigold (Tagetes erecta)

2020 ◽  
Author(s):  
Chunling Zhang ◽  
Yalin Sun ◽  
Ludan Wei ◽  
Wenjing Wang ◽  
Hang Li ◽  
...  
Keyword(s):  
Profile Analysis ◽  
Floral Organ ◽  
Tagetes Erecta ◽  
Functional Conservation ◽  
Floral Buds ◽  
Expression Profile Analysis ◽  
Petal Identity ◽  
Organ Identity ◽  
Insight Into

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.

scholarly journals The Orchid MADS-Box Genes Controlling Floral Morphogenesis

2006 ◽  
Vol 6 ◽  
pp. 1933-1944 ◽  
Author(s):  
Wen-Chieh Tsai ◽  
Hong-Hwa Chen
Keyword(s):  
Floral Organ ◽  
Mads Box ◽  
Mads Box Genes ◽  
Floral Diversity ◽  
Physiological Properties ◽  
Abcde Model ◽  
New Variant ◽  
Organ Identity ◽  
Genes Encoding ◽  
Highly Evolved

Orchids are known for both their floral diversity and ecological strategies. The versatility and specialization in orchid floral morphology, structure, and physiological properties have fascinated botanists for centuries. In floral studies, MADS-box genes contributing to the now famous ABCDE model of floral organ identity control have dominated conceptual thinking. The sophisticated orchid floral organization offers an opportunity to discover new variant genes and different levels of complexity to the ABCDE model. Recently, several remarkable research studies done on orchid MADS-box genes have revealed the important roles on orchid floral development. Knowledge about MADS-box genes’' encoding ABCDE functions in orchids will give insights into the highly evolved floral morphogenetic networks of orchids.

scholarly journals Pitfall Flower Development and Organ Identity of Ceropegia sandersonii (Apocynaceae-Asclepiadoideae)

Plants ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1767
Author(s):  
Annemarie Heiduk ◽  
Dewi Pramanik ◽  
Marlies Spaans ◽  
Loes Gast ◽  
Nemi Dorst ◽  
...  
Keyword(s):  
Gene Expression ◽  
Floral Anatomy ◽  
Floral Organ ◽  
Mads Box ◽  
Floral Organs ◽  
Abcde Model ◽  
Organ Identity ◽  
Mads Box Gene ◽  
Flower Evolution ◽  
Developmental Phases

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.

Alteration of tobacco floral organ identity by expression of combinations of Antirrhinum MADS-box genes

1996 ◽  
Vol 10 (4) ◽  
pp. 663-677 ◽  
Author(s):  
Brendan Davies ◽  
Alexandra Rosa ◽  
Tinka Eneva ◽  
Heinz Saedler ◽  
Hans Sommer
Keyword(s):  
Floral Organ ◽  
Mads Box ◽  
Mads Box Genes ◽  
Floral Organ Identity ◽  
Organ Identity

scholarly journals CHIMERIC FLORAL ORGANS1, Encoding a Monocot-Specific MADS Box Protein, Regulates Floral Organ Identity in Rice

2012 ◽  
Vol 160 (2) ◽  
pp. 788-807 ◽  
Author(s):  
Xianchun Sang ◽  
Yunfeng Li ◽  
Zengke Luo ◽  
Deyong Ren ◽  
Likui Fang ◽  
...  
Keyword(s):  
Floral Organ ◽  
Mads Box ◽  
Floral Organ Identity ◽  
Organ Identity

scholarly journals GmAGL1, a MADS-Box Gene from Soybean, Is Involved in Floral Organ Identity and Fruit Dehiscence

2017 ◽  
Vol 8 ◽  
Author(s):  
Yingjun Chi ◽  
Tingting Wang ◽  
Guangli Xu ◽  
Hui Yang ◽  
Xuanrui Zeng ◽  
...  
Keyword(s):  
Floral Organ ◽  
Mads Box ◽  
Floral Organ Identity ◽  
Organ Identity ◽  
Mads Box Gene ◽  
Fruit Dehiscence

scholarly journals MADS-box genes are involved in floral development and evolution.

2001 ◽  
Vol 48 (2) ◽  
pp. 351-358 ◽  
Author(s):  
H Saedler ◽  
A Becker ◽  
K U Winter ◽  
C Kirchner ◽  
G Theissen
Keyword(s):  
Floral Development ◽  
Higher Plants ◽  
Control Cell ◽  
Floral Organ ◽  
Reproductive Organs ◽  
Mads Box ◽  
Mads Box Genes ◽  
Flower Bud ◽  
Organ Identity ◽  
Eukaryotic Organisms

MADS-box genes encode transcription factors in all eukaryotic organisms thus far studied. Plant MADS-box proteins contain a DNA-binding (M), an intervening (I), a Keratin-like (K) and a C-terminal C-domain, thus plant MADS-box proteins are of the MIKC type. In higher plants most of the well-characterized genes are involved in floral development. They control the transition from vegetative to generative growth and determine inflorescence meristem identity. They specify floral organ identity as outlined in the ABC model of floral development. Moreover, in Antirrhinum majus the MADS-box gene products DEF/GLO and PLE control cell proliferation in the developing flower bud. In this species the DEF/GLO and the SQUA proteins form a ternary complex which determines the overall "Bauplan" of the flower. Phylogenetic reconstructions of MADS-box sequences obtained from ferns, gymnosperms and higher eudicots reveal that, although ferns possess already MIKC type genes, these are not orthologous to the well characterized MADS-box genes from gymnosperms or angiosperms. Putative orthologs of floral homeotic B- and C-function genes have been identified in different gymnosperms suggesting that these genes evolved some 300-400 million years ago. Both gymnosperms and angiosperms also contain a hitherto unknown sister clade of the B-genes, which we termed Bsister. A novel hypothesis will be described suggesting that B and Bsister might be involved in sex determination of male and female reproductive organs, respectively.

Sign in / Sign up

Export Citation Format

Share Document