Genomic characterization of miR156 and SQUAMOSA promoter binding protein-like genes in sweet orange (Citrus sinensis)

2017 ◽  
Vol 130 (1) ◽  
pp. 103-116 ◽  
Author(s):  
Mei-Ya Liu ◽  
Xiao-Meng Wu ◽  
Jian-Mei Long ◽  
Wen-Wu Guo
2005 ◽  
Vol 47 (12) ◽  
pp. 1507-1515 ◽  
Author(s):  
Neng-Guo TAO ◽  
Juan XU ◽  
Yun-Jiang CHENG ◽  
Liu HONG ◽  
Wen-Wu GUO ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e104182 ◽  
Author(s):  
Manosh Kumar Biswas ◽  
Qiang Xu ◽  
Christoph Mayer ◽  
Xiuxin Deng

Genome ◽  
2010 ◽  
Vol 53 (10) ◽  
pp. 816-823 ◽  
Author(s):  
Jing Fan ◽  
Chunxian Chen ◽  
Qibin Yu ◽  
Zheng-Guo Li ◽  
Frederick G. Gmitter

Three putative terpenoid UDP-glycosyltransferase (UGT) genes, designated CsUGT1, CsUGT2, and CsUGT3, were isolated and characterized in ‘Valencia’ sweet orange ( Citrus sinensis L. Osbeck). CsUGT1 consisted of 1493 nucleotides with an open reading frame encoding 492 amino acids, CsUGT2 consisted of 1727 nucleotides encoding 504 amino acids, and CsUGT3 consisted of 1705 nucleotides encoding 468 amino acids. CsUGT3 had a 145 bp intron at 730–874, whereas CsUGT1 and CsUGT2 had none. The three deduced glycosyltransferase proteins had a highly conserved plant secondary product glycosyltransferase motif in the C terminus. Phylogenetic analysis showed that CsUGT1 and CsUGT3 were classified into group L of glycosyltransferase family 1, and CsUGT2 was classified into group D. Through Southern blotting analysis, CsUGT1 was found to have two copies in the sweet orange genome, whereas CsUGT2 and CsUGT3 had at least seven and nine copies, respectively. CsUGT1, CsUGT2, and CsUGT3 were constitutively expressed in leaf, flower, and fruit tissues. The results facilitate further investigation of the function of terpenoid glycosyltransferases in citrus and the biosynthesis of terpenoid glycosides in vitro.


2010 ◽  
Vol 20 (2) ◽  
pp. 89-96 ◽  
Author(s):  
Ruth C. Martin ◽  
Masashi Asahina ◽  
Po-Pu Liu ◽  
Jessica R. Kristof ◽  
Jennifer L. Coppersmith ◽  
...  

AbstractGermination and early seedling development are critical for successful stand establishment of plants. Following germination, the cotyledons, which are derived from embryonic tissue, emerge from the seed. Arabidopsis seedlings at post-germinative stages are supported mainly by the supply of nutrition from the cotyledons until vegetative leaves emerge and initiate photosynthesis. The switch to autotrophic growth is a significant transition at the post-germinative stage. Here, we provide evidence that down-regulation of SQUAMOSA PROMOTER-BINDING PROTEIN LIKE13 (SPL13) by microRNA156 (miR156) plays an important role in the regulation of the post-germinative switch from the cotyledon stage to the vegetative-leaf stage. Silent mutations created in the SPL13 sequence in the region that is complementary to the miR156 sequence caused the deregulation of the mutant form of SPL13 (mSPL13) mRNA from miR156. Mutant seedlings over-accumulated miRNA-resistant messages and exhibited a delay in the emergence of vegetative leaves compared to wild-type seedlings. The delay was not observed in control transgenic plants expressing non-mutated SPL13, indicating that the phenotype was caused specifically by the silent mutations and deregulation of SPL13 from miR156. Characterization of the SPL13 promoter indicated that this gene is expressed mainly in the hypocotyl and affects leaf primordium development. These results suggest that the repression of SPL13 by miR156 is essential for normal post-germinative growth in Arabidopsis.


Author(s):  
K. Dhanasekaran ◽  
M. Mohamed Musthafa ◽  
M. Dharmendirakumar

2009 ◽  
Vol 120 (1) ◽  
pp. 70-76 ◽  
Author(s):  
Ehsan Ullah Khan ◽  
Xing-Zheng Fu ◽  
Jing Wang ◽  
Qi-Jun Fan ◽  
Xiao-San Huang ◽  
...  

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