scholarly journals Recent advances in flower color variation and patterning of Japanese morning glory and petunia

2018 ◽  
Vol 68 (1) ◽  
pp. 128-138 ◽  
Author(s):  
Yasumasa Morita ◽  
Atsushi Hoshino

This chapter revisits the author's doctoral work on the maintenance of flower color variation in morning glories to explore how a feminist analysis can help explain the shape and scope of this research. It traces the idea of variation and the shifting understanding of its significance in the field of evolutionary biology and moreover posits that an interdisciplinary education would have fundamentally reshaped the author's work on the evolutionary biology of morning glory flower color variation. Thus, inspired by the touch-sensitive thigmatropic tendrils of morning glories, which allow the plants to scale large objects and burrow into narrow crevices, this chapter narrates tales of the morning glories through the curious and adventurous tendrils of naturecultural storytelling.


2019 ◽  
Vol 60 (8) ◽  
pp. 1871-1879 ◽  
Author(s):  
Atsushi Hoshino ◽  
Takayuki Mizuno ◽  
Keiichi Shimizu ◽  
Shoko Mori ◽  
Sachiko Fukada-Tanaka ◽  
...  

Abstract Wild-type plants of the Japanese morning glory (Ipomoea nil) produce blue flowers that accumulate anthocyanin pigments, whereas its mutant cultivars show wide range flower color such as red, magenta and white. However, I. nil lacks yellow color varieties even though yellow flowers were curiously described in words and woodblocks printed in the 19th century. Such yellow flowers have been regarded as ‘phantom morning glories’, and their production has not been achieved despite efforts by breeders of I. nil. The chalcone isomerase (CHI) mutants (including line 54Y) bloom very pale yellow or cream-colored flowers conferred by the accumulation of 2′, 4′, 6′, 4-tetrahydoroxychalcone (THC) 2′-O-glucoside. To produce yellow phantom morning glories, we introduced two snapdragon (Antirrhinum majus) genes to the 54Y line by encoding aureusidin synthase (AmAS1) and chalcone 4′-O-glucosyltransferase (Am4′CGT), which are necessary for the accumulation of aureusidin 6-O-glucoside and yellow coloration in A. majus. The transgenic plants expressing both genes exhibit yellow flowers, a character sought for many years. The flower petals of the transgenic plants contained aureusidin 6-O-glucoside, as well as a reduced amount of THC 2′-O-glucoside. In addition, we identified a novel aurone compound, aureusidin 6-O-(6″-O-malonyl)-glucoside, in the yellow petals. A combination of the coexpression of AmAS1 and Am4′CGT and suppression of CHI is an effective strategy for generating yellow varieties in horticultural plants.


2013 ◽  
Vol 47 (5) ◽  
pp. 437-453
Author(s):  
Zhu Manlan ◽  
Wang Liangsheng ◽  
Zhang Huijin ◽  
Xu Yanjun ◽  
Zheng Xuchen ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Yu Qiao ◽  
Qiming Cheng ◽  
Yutong Zhang ◽  
Wei Yan ◽  
Fengyan Yi ◽  
...  

Abstract Background Sainfoin (Onobrychis viciifolia Scop) is not only a high-quality legume forage, but also a nectar-producing plant. Therefore, the flower color of sainfoin is an important agronomic trait, but the factors affecting its flower phenotype are still unclear. To gain insights into the regulatory networks associated with metabolic pathways of coloration compounds (flavonoids or anthocyanins) and identify the key genes, we conducted a comprehensive analysis of the phenotype, metabolome and transcriptome of WF and AF of sainfoin. Results Delphinidin, petunidin and malvidin derivatives were the main anthocyanin compounds in the AF of sainfoin. These substances were not detected in the WF of sainfoin. The transcriptomes of WF and AF in sainfoin at the S1 and S3 stages were obtained using the Illumina HiSeq4000 platform. Overall, 10,166 (4273 upregulated and 5893 downregulated) and 15,334 (8174 upregulated and 7160 downregulated) DEGs were identified in flowers at S1 and S3 stages, respectively (WF-VS-AF). KEGG pathway annotations showed that 6396 unigenes were annotated to 120 pathways and contained 866 DEGs at S1 stages, and 6396 unigenes were annotated to 131 pathways and included 1546 DEGs at the S3 stage. Nine DEGs belonging to the “flavonoid biosynthesis”and “phenylpropanoid biosynthesis” pathways involved in flower color formation were identified and verified by RT-qPCR analyses. Among these DEGs, 4CL3, FLS, ANS, CHS, DFR and CHI2 exhibited downregulated expression, and F3H exhibited upregulated expression in the WF compared to the AF, resulting in a decrease in anthocyanin synthesis and the formation of WF in sainfoin. Conclusions This study is the first to use transcriptome technology to study the mechanism of white flower formation in sainfoin. Our transcriptome data will be a great enrichment of the genetic information for sainfoin. In addition, the data presented herein will provide valuable molecular information for genetic breeding and provide insight into the future study of flower color polymorphisms in sainfoin.


ChemInform ◽  
2010 ◽  
Vol 32 (48) ◽  
pp. no-no
Author(s):  
Kenjiro Toki ◽  
Norio Saito ◽  
Shigeru Iida ◽  
Atsushi Hoshino ◽  
Atsushi Shigihara ◽  
...  

2009 ◽  
Vol 122 (2) ◽  
pp. 223-223
Author(s):  
Atsushi Hoshino ◽  
Kyeung-Il Park ◽  
Shigeru Iida

2018 ◽  
Vol 40 (3) ◽  
Author(s):  
Lixia Sheng ◽  
Wei Xia ◽  
Shu Zang ◽  
Yuqian Zeng ◽  
Xiaoyu Yuan ◽  
...  

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