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

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.

2006 ◽  
Vol 6 ◽  
pp. 1933-1944 ◽  
Author(s):  
Wen-Chieh Tsai ◽  
Hong-Hwa Chen

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.


1996 ◽  
Vol 10 (4) ◽  
pp. 663-677 ◽  
Author(s):  
Brendan Davies ◽  
Alexandra Rosa ◽  
Tinka Eneva ◽  
Heinz Saedler ◽  
Hans Sommer

2017 ◽  
Vol 63 (4) ◽  
Author(s):  
Aleksandra Smoczynska ◽  
Zofia Szweykowska-Kulinska

Flower structure in grasses is very unique. There are no petals or sepals like in eudicots but instead flowers develop bract-like structures –palea and lemma. Reproductive organs are enclosed by round lodicule that not only protects reproductive organs but also play important role during flower opening. First genetic model for floral organ development was proposed 25 years ago and it was based on the research on model eudicots. Since then studies have been made to answer the question whether this model could be applicable in case of monocots. Genes from all found in eudicots classes have been also indentified in genomes of such monocots like rice, maize or barley. What’s more it seems that miRNA-mediated regulation of floral organ genes that was observed in case of Arabidopsis thaliana also has a place in monocots. MiRNA172, miRNA159, miRNA171 and miRNA396 regulate expression of floral organ identity genes in barley, rice and maize affecting various features of flower structure from formation of lemma and palea to development of reproductive organs. Model of floral development in grasses and its genetic regulation in not yet fully characterized. Further studies on both model eudicots and grasses are needed to unravel this topic. This review provides general overview of genetic model of flower organ identity specification in monocots and it’s miRNA-mediated regulation.


2011 ◽  
Vol 52 (9) ◽  
pp. 1515-1531 ◽  
Author(s):  
Zhao-Jun Pan ◽  
Chih-Chin Cheng ◽  
Wen-Chieh Tsai ◽  
Mei-Chu Chung ◽  
Wen-Huei Chen ◽  
...  

Nature ◽  
2000 ◽  
Vol 405 (6783) ◽  
pp. 200-203 ◽  
Author(s):  
Soraya Pelaz ◽  
Gary S. Ditta ◽  
Elvira Baumann ◽  
Ellen Wisman ◽  
Martin F. Yanofsky

2006 ◽  
Vol 6 ◽  
pp. 1923-1932 ◽  
Author(s):  
Takahiro Yamaguchi ◽  
Hiro-Yuki Hirano

MADS-box genes play critical roles in a number of developmental processes in flowering plants, such as specification of floral organ identity, control of flowering time, and regulation of fruit development. Because of their crucial functions in flower development, diversification of the MADS-box gene family has been suggested to be a major factor responsible for floral diversity during radiation of the flowering plants. Inflorescences and flowers in the grass species have unique structures that are distinct from those in eudicots. Thus, it is plausible that the diversification of the function of MADS-box genes may have been a key driving force in the morphological divergence of the flowers and inflorescences in the grasses. Indeed, recent progress in genetic studies has shown that MADS-box genes function in flower development inOryza sativa(rice), in support of the idea that functional diversification of the MADS-box genes was involved in evolution of the angiosperms. In this review, we summarize the functions of the major subfamilies of the MADS-box genes in rice and discuss their role in the development and evolution of rice flowers and inflorescences.


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