» Articles » PMID: 27487946

Evolutionary and Functional Analysis of Mulberry Type III Polyketide Synthases

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2016 Aug 5
PMID 27487946
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Type III polyketide synthases are important for the biosynthesis of flavonoids and various plant polyphenols. Mulberry plants have abundant polyphenols, but very little is known about the mulberry type III polyketide synthase genes. An analysis of these genes may provide new targets for genetic improvement to increase relevant secondary metabolites and enhance the plant tolerance to biotic and abiotic stresses.

Results: Eighteen genes encoding type III polyketide synthases were identified, including six chalcone synthases (CHS), ten stilbene synthases (STS), and two polyketide synthases (PKS). Functional characterization of four genes representing most of the MnCHS and MnSTS genes by coexpression with 4-Coumaroyl-CoA ligase in Escherichia coli indicated that their products were able to catalyze p-coumaroyl-CoA and malonyl-CoA to generate naringenin and resveratrol, respectively. Microsynteny analysis within mulberry indicated that segmental and tandem duplication events contributed to the expansion of the MnCHS family, while tandem duplications were mainly responsible for the generation of the MnSTS genes. Combining the evolution and expression analysis results of the mulberry type III PKS genes indicated that MnCHS and MnSTS genes evolved mainly under purifying selection to maintain their original functions, but transcriptional subfunctionalization occurred during long-term species evolution. Moreover, mulberry leaves can rapidly accumulated oxyresveratrol after UV-C irradiation, suggesting that resveratrol was converted to oxyresveratrol.

Conclusions: Characterizing the functions and evolution of mulberry type III PKS genes is crucial for advancing our understanding of these genes and providing the basis for further studies on the biosynthesis of relevant secondary metabolites in mulberry plants.

Citing Articles

Unraveling Whole-Genome Sequence and Functional Characterization of PH3.

Zhang X, Liang J, Zhang D, Wang L, Ye S Foods. 2024; 13(22).

PMID: 39593971 PMC: 11593290. DOI: 10.3390/foods13223555.


Understanding metabolic diversification in plants: branchpoints in the evolution of specialized metabolism.

Ji W, Osbourn A, Liu Z Philos Trans R Soc Lond B Biol Sci. 2024; 379(1914):20230359.

PMID: 39343032 PMC: 11439499. DOI: 10.1098/rstb.2023.0359.


Rhizophagus Irregularis regulates flavonoids metabolism in paper mulberry roots under cadmium stress.

Deng S, Pan L, Ke T, Liang J, Zhang R, Chen H Mycorrhiza. 2024; 34(4):317-339.

PMID: 38836935 DOI: 10.1007/s00572-024-01155-7.


The Stilbene Synthase Family in : A Genome-Wide Study and Functional Characterization in Response to Stress.

Brasileiro A, Gimenes M, Pereira B, Mota A, Aguiar M, Martins A Genes (Basel). 2023; 14(12).

PMID: 38137003 PMC: 10742623. DOI: 10.3390/genes14122181.


Impact of Environmental Factors on Stilbene Biosynthesis.

Valletta A, Iozia L, Leonelli F Plants (Basel). 2021; 10(1).

PMID: 33406721 PMC: 7823792. DOI: 10.3390/plants10010090.


References
1.
Sigrist C, de Castro E, Cerutti L, Cuche B, Hulo N, Bridge A . New and continuing developments at PROSITE. Nucleic Acids Res. 2012; 41(Database issue):D344-7. PMC: 3531220. DOI: 10.1093/nar/gks1067. View

2.
Austin M, Bowman M, Ferrer J, Schroder J, Noel J . An aldol switch discovered in stilbene synthases mediates cyclization specificity of type III polyketide synthases. Chem Biol. 2004; 11(9):1179-94. DOI: 10.1016/j.chembiol.2004.05.024. View

3.
Yang Z, Swanson W . Codon-substitution models to detect adaptive evolution that account for heterogeneous selective pressures among site classes. Mol Biol Evol. 2001; 19(1):49-57. DOI: 10.1093/oxfordjournals.molbev.a003981. View

4.
Saitou N, Nei M . The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol. 1987; 4(4):406-25. DOI: 10.1093/oxfordjournals.molbev.a040454. View

5.
Morita H, Kondo S, Oguro S, Noguchi H, Sugio S, Abe I . Structural insight into chain-length control and product specificity of pentaketide chromone synthase from Aloe arborescens. Chem Biol. 2007; 14(4):359-69. DOI: 10.1016/j.chembiol.2007.02.003. View