scholarly journals Functional divergence within class B MADS-box genes TfGLO and TfDEF in Torenia fournieri Lind

2010 ◽  
Vol 284 (5) ◽  
pp. 399-414 ◽  
Author(s):  
Katsutomo Sasaki ◽  
Ryutaro Aida ◽  
Hiroyasu Yamaguchi ◽  
Masahito Shikata ◽  
Tomoya Niki ◽  
...  
2013 ◽  
Vol 170 (4) ◽  
pp. 424-431 ◽  
Author(s):  
Bo Wei ◽  
Danmei Liu ◽  
Juanjuan Guo ◽  
Charles H. Leseberg ◽  
Xiangqi Zhang ◽  
...  

Plant Science ◽  
2001 ◽  
Vol 161 (3) ◽  
pp. 549-557 ◽  
Author(s):  
Kentaro Kitahara ◽  
Sayaka Hirai ◽  
Hirokazu Fukui ◽  
Shogo Matsumoto
Keyword(s):  
Mads Box ◽  

2004 ◽  
Vol 73 (3) ◽  
pp. 208-215 ◽  
Author(s):  
Kentaro Kitahara ◽  
Tomomi Ohtsubo ◽  
Junichi Soejima ◽  
Shogo Matsumoto
Keyword(s):  
Mads Box ◽  

2021 ◽  
Vol 28 (1) ◽  
Author(s):  
Gangxu Shen ◽  
Yong Jia ◽  
Wei-Lung Wang

Abstract Background MADS-box transcription factors function as homo- or heterodimers and regulate many aspects of plant development; moreover, MADS-box genes have undergone extensive duplication and divergence. For example, the morphological diversity of floral organs is closely related to the functional divergence of the MADS-box gene family. B-class genes (such as Arabidopsis thaliana APETALA3 [AP3] and PISTILLATA [PI]) belong to a subgroup of MADS-box genes. Here, we collected 97 MADS-box B protein sequences from 21 seed plant species and examined their motifs to better understand the functional evolution of B proteins. Results We used the MEME tool to identify conserved sequence motifs in these B proteins; unique motif arrangements and sequences were identified in these B proteins. The keratin-like domains of Malus domestica and Populus trichocarpa B proteins differed from those in other angiosperms, suggesting that a novel regulatory network might have evolved in these species. The MADS domains of Nelumbo nucifera, Glycine max, and Amborella trichopoda B-proteins contained motif 9; in contrast, those of other plants contained motif 1. Protein modelling analyses revealed that MADS domains with motif 9 may lack amino acid sites required for DNA-binding. These results suggested that the three species might share an alternative mechanism controlling floral development. Conclusions Amborella trichopoda has B proteins with either motif 1 or motif 9 MADS domains, suggesting that these two types of MADS domains evolved from the ancestral domain into two groups, those with motif 9 (N. nucifera and G. max), and those with motif 1. Moreover, our results suggest that the homodimer/heterodimer intermediate transition structure first appeared in A. trichopoda. Therefore, our systematic analysis of the motifs in B proteins sheds light on the evolution of these important transcription factors.


2021 ◽  
Vol 22 (13) ◽  
pp. 7025
Author(s):  
Francesca Lucibelli ◽  
Maria Carmen Valoroso ◽  
Günter Theißen ◽  
Susanne Nolden ◽  
Mariana Mondragon-Palomino ◽  
...  

The molecular basis of orchid flower development is accomplished through a specific regulatory program in which the class B MADS-box AP3/DEF genes play a central role. In particular, the differential expression of four class B AP3/DEF genes is responsible for specification of organ identities in the orchid perianth. Other MADS-box genes (AGL6 and SEP-like) enrich the molecular program underpinning the orchid perianth development, resulting in the expansion of the original “orchid code” in an even more complex gene regulatory network. To identify candidates that could interact with the AP3/DEF genes in orchids, we conducted an in silico differential expression analysis in wild-type and peloric Phalaenopsis. The results suggest that a YABBY DL-like gene could be involved in the molecular program leading to the development of the orchid perianth, particularly the labellum. Two YABBY DL/CRC homologs are present in the genome of Phalaenopsis equestris, PeDL1 and PeDL2, and both express two alternative isoforms. Quantitative real-time PCR analyses revealed that both genes are expressed in column and ovary. In addition, PeDL2 is more strongly expressed the labellum than in the other tepals of wild-type flowers. This pattern is similar to that of the AP3/DEF genes PeMADS3/4 and opposite to that of PeMADS2/5. In peloric mutant Phalaenopsis, where labellum-like structures substitute the lateral inner tepals, PeDL2 is expressed at similar levels of the PeMADS2-5 genes, suggesting the involvement of PeDL2 in the development of the labellum, together with the PeMADS2-PeMADS5 genes. Although the yeast two-hybrid analysis did not reveal the ability of PeDL2 to bind the PeMADS2-PeMADS5 proteins directly, the existence of regulatory interactions is suggested by the presence of CArG-boxes and other MADS-box transcription factor binding sites within the putative promoter of the orchid DL2 gene.


2014 ◽  
pp. 93-98
Author(s):  
N. Okuzumi ◽  
M. Otani ◽  
H. Otsubo ◽  
S. Meguro ◽  
Y. Hara ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Dandan Meng ◽  
Yunpeng Cao ◽  
Tianzhe Chen ◽  
Muhammad Abdullah ◽  
Qing Jin ◽  
...  

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