scholarly journals INHERITANCE IN THE CARNATION, DIANTHUS CARYOPHYLLUS. V. THE CHEMISTRY OF FLOWER COLOR VARIATION, II

Genetics ◽  
1956 ◽  
Vol 41 (1) ◽  
pp. 93-97
Author(s):  
T A Geissman ◽  
E H Hinreiner ◽  
E C Jorgensen
2019 ◽  
Vol 88 (1) ◽  
pp. 116-128 ◽  
Author(s):  
Hayato Morimoto ◽  
Takako Narumi-Kawasaki ◽  
Takejiro Takamura ◽  
Seiichi Fukai

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.


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

Plant Science ◽  
2020 ◽  
Vol 299 ◽  
pp. 110598
Author(s):  
Hayato Morimoto ◽  
Takako Narumi-Kawasaki ◽  
Takejiro Takamura ◽  
Seiichi Fukai

2019 ◽  
Vol 20 (19) ◽  
pp. 4743 ◽  
Author(s):  
Hongli Liu ◽  
Qian Lou ◽  
Junren Ma ◽  
Beibei Su ◽  
Zhuangzhuang Gao ◽  
...  

Grape hyacinth (Muscari spp.) is a popular ornamental plant with bulbous flowers noted for their rich blue color. Muscari species have been thought to accumulate delphinidin and cyanidin rather than pelargonidin-type anthocyanins because their dihydroflavonol 4-reductase (DFR) does not efficiently reduce dihydrokaempferol. In our study, we clone a novel DFR gene from blue flowers of Muscari. aucheri. Quantitative real-time PCR (qRT-PCR) and anthocyanin analysis showed that the expression pattern of MaDFR had strong correlations with the accumulation of delphinidin, relatively weak correlations with cyanidin, and no correations with pelargonidin. However, in vitro enzymatic analysis revealed that the MaDFR enzyme can reduce all the three types of dihydroflavonols (dihydrokaempferol, dihydroquercetin, and dihydromyricetin), although it most preferred dihydromyricetin as a substrate to produce leucodelphinidin, the precursor of blue-hued delphinidin. This indicated that there may be other functional genes responsible for the loss of red pelargonidin-based pigments in Muscari. To further verify the substrate-specific selection domains of MaDFR, an assay of amino acid substitutions was conducted. The activity of MaDFR was not affected whenever the N135 or E146 site was mutated. However, when both of them were mutated, the catalytic activity of MaDFR was lost completely. The results suggest that both the N135 and E146 sites are essential for the activity of MaDFR. Additionally, the heterologous expression of MaDFR in tobacco (Nicotiana tabacum) resulted in increasing anthocyanin accumulation, leading to a darker flower color, which suggested that MaDFR was involved in color development in flowers. In summary, MaDFR has a high preference for dihydromyricetin, and it could be a powerful candidate gene for genetic engineering for blue flower colour modification. Our results also make a valuable contribution to understanding the basis of color variation in the genus Muscari.


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.


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