scholarly journals Changes at a Critical Branchpoint in the Anthocyanin Biosynthetic Pathway Underlie the Blue to Orange Flower Color Transition in Lysimachia arvensis

2021 ◽  
Vol 12 ◽  
Author(s):  
Mercedes Sánchez-Cabrera ◽  
Francisco Javier Jiménez-López ◽  
Eduardo Narbona ◽  
Montserrat Arista ◽  
Pedro L. Ortiz ◽  
...  

Anthocyanins are the primary pigments contributing to the variety of flower colors among angiosperms and are considered essential for survival and reproduction. Anthocyanins are members of the flavonoids, a broader class of secondary metabolites, of which there are numerous structural genes and regulators thereof. In western European populations of Lysimachia arvensis, there are blue- and orange-petaled individuals. The proportion of blue-flowered plants increases with temperature and daylength yet decreases with precipitation. Here, we performed a transcriptome analysis to characterize the coding sequences of a large group of flavonoid biosynthetic genes, examine their expression and compare our results to flavonoid biochemical analysis for blue and orange petals. Among a set of 140 structural and regulatory genes broadly representing the flavonoid biosynthetic pathway, we found 39 genes with significant differential expression including some that have previously been reported to be involved in similar flower color transitions. In particular, F3′5′H and DFR, two genes at a critical branchpoint in the ABP for determining flower color, showed differential expression. The expression results were complemented by careful examination of the SNPs that differentiate the two color types for these two critical genes. The decreased expression of F3′5′H in orange petals and differential expression of two distinct copies of DFR, which also exhibit amino acid changes in the color-determining substrate specificity region, strongly correlate with the blue to orange transition. Our biochemical analysis was consistent with the transcriptome data indicating that the shift from blue to orange petals is caused by a change from primarily malvidin to largely pelargonidin forms of anthocyanins. Overall, we have identified several flavonoid biosynthetic pathway loci likely involved in the shift in flower color in L. arvensis and even more loci that may represent the complex network of genetic and physiological consequences of this flower color polymorphism.

Genetika ◽  
2019 ◽  
Vol 51 (1) ◽  
pp. 93-102
Author(s):  
Klára Stiasna ◽  
Mária Presinszká ◽  
Tomás Vyhnánek ◽  
Václav Trojan ◽  
Pavel Hanácek ◽  
...  

The DNA sequences of chosen structural genes, flavanone 3-hydroxylase (F3H) and dihydroflavonol 4-reductase (DFR), encoding key enzymes from the flavonoid biosynthetic pathway, were studied in this paper. Sequences were gained using different approaches, i.e. direct sequencing from the PCR product for F3H and a cloning strategy for DFR. Five bread wheat (Triticum aestivum L.) genotypes with nonstandard coloured caryopses, purple, blue, and white, were used as plant material. The sequence variability was observed among tested genotypes.


Genes ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 31
Author(s):  
Jingying Zhang ◽  
Changhai Sui ◽  
Yanli Wang ◽  
Shuying Liu ◽  
Huimin Liu ◽  
...  

Background: Hosta plantaginea (Lam.) Aschers (HPA), a species in the family Liliaceae, is an important landscaping plant and herbaceous ornamental flower. However, because the flower has only two colors, white and purple, color matching applications are extremely limited. To date, the mechanism underlying flower color regulation remains unclear. Methods: In this study, the transcriptomes of three cultivars—H. plantaginea (HP, white flower), H. Cathayana (HC, purple flower), and H. plantaginea ‘Summer Fragrance’ (HS, purple flower)—at three flowering stages (bud stage, initial stage, and late flowering stage) were sequenced with the Illumina HiSeq 2000 (San Diego, CA, USA). The RNA-Seq results were validated by qRT-PCR of eight differentially expressed genes (DEGs). Then, we further analyzed the relationship between anthocyanidin synthase (ANS), chalcone synthase (CHS), and P450 and the flower color regulation by Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Eukaryotic Orthologous Groups (KOG) network and pathway enrichment analyses. The overexpression of CHS and ANS in transgenic tobacco petals was verified using qRT-PCR, and the petal colors associated with the overexpression lines were confirmed using absorbance values. Results: Over 434,349 transcripts were isolated, and 302,832 unigenes were identified. Additionally, through transcriptome comparisons, 2098, 722, and 606 DEGs between the different stages were found for HP, HC, and HS, respectively. Furthermore, GO and KEGG pathway analyses showed that 84 color-related DEGs were enriched in 22 pathways. In particular, the flavonoid biosynthetic pathway, regulated by CHS, ANS, and the cytochrome P450-type monooxygenase gene, was upregulated in both purple flower varieties in the late flowering stage. In contrast, this gene was hardly expressed in the white flower variety, which was verified in the CHS and ANS overexpression transgenic tobacco petals. Conclusions: The results suggest that CHS, ANS, and the cytochrome P450s-regulated flavonoid biosynthetic pathway might play key roles in the regulation of flower color in HPA. These insights into the mechanism of flower color regulation could be used to guide artificial breeding of polychrome varieties of ornamental flowers.


2010 ◽  
Vol 74 (9) ◽  
pp. 1760-1769 ◽  
Author(s):  
Yoshikazu TANAKA ◽  
Filippa BRUGLIERA ◽  
Gianna KALC ◽  
Mick SENIOR ◽  
Barry DYSON ◽  
...  

2002 ◽  
Vol 127 (6) ◽  
pp. 947-956 ◽  
Author(s):  
R.J. Griesbach

A regulatory gene, An2, controls structural genes within the flavonoid biosynthetic pathway. The inheritance of An2 expression in crosses between P. axillaris (an2) and P. exserta (An2+) was studied. Floral pigmentation was quantitatively inherited and involved the expression of a single regulatory gene (An2) and three structural genes (Hf1, An6 and Fl). White flowers were produced in an2- genotypes; while pigmented flowers were produced in An2+ genotypes. The intensity of pigmentation was determined by the interaction of An2 with An6, Hf1 and Fl, as well as substrate competition between the An6 and Fl encoded enzymes.


2016 ◽  
Vol 7 ◽  
Author(s):  
Inés Casimiro-Soriguer ◽  
Eduardo Narbona ◽  
M. L. Buide ◽  
José C. del Valle ◽  
Justen B. Whittall

PLoS ONE ◽  
2015 ◽  
Vol 10 (3) ◽  
pp. e0119054 ◽  
Author(s):  
Wei Sun ◽  
Xiangyu Meng ◽  
Lingjie Liang ◽  
Wangshu Jiang ◽  
Yafei Huang ◽  
...  

2006 ◽  
Vol 23 (1) ◽  
pp. 19-24 ◽  
Author(s):  
Yukiko Ueyama ◽  
Yukihisa Katsumoto ◽  
Yuko Fukui ◽  
Masako Fukuchi-Mizutani ◽  
Hideo Ohkawa ◽  
...  

Gene ◽  
2018 ◽  
Vol 676 ◽  
pp. 279-289 ◽  
Author(s):  
Nan Yang ◽  
Kaige Zhao ◽  
Xiang Li ◽  
Rong Zhao ◽  
Muhammad z Aslam ◽  
...  

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