Construction of a high-density genetic map for yardlong bean and identification of ANT1 as a regulator of anthocyanin biosynthesis

Hongmei Zhang , Wei Zhang , Shan Meng , Linchong Hui , Xiaoqing Liu , Wei Chen , Wei Yan , Xin Chen , Huatao Chen

Horticulture Research ›› 2024, Vol. 11 ›› Issue (1) : 247

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Horticulture Research ›› 2024, Vol. 11 ›› Issue (1) : 247 DOI: 10.1093/hr/uhad247
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Construction of a high-density genetic map for yardlong bean and identification of ANT1 as a regulator of anthocyanin biosynthesis

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Abstract

Because its long, tender pods supply essential proteins, vitamins, and fibers to humans, yardlong bean (Vigna unguiculata ssp. sesquipedalis) is a commonly consumed vegetable, especially in Southeast Asia. To provide insights into the genetic bases of key agricultural traits in yardlong bean, we here created a high-density bin-map with 2084 bin markers using 514 227 SNPs from a recombinant-inbred line (RIL) population. Quantitative trait loci (QTL) mapping was carried out to identify loci associated with anthocyanin content (ANT), vitamin E content (VE), total soluble protein content (TSP), pod length (PL), hundred-seed weight (HSW), seed length and width (SL and SW, respectively), and seed coat color (SCC). In total, 20 related QTLs were isolated, explaining 7.58-56.03% of the phenotypic variation. Of these, five major QTLs (qANT5, qTSP11, qVE7, qPL3, and qSCC9) were detected in 2020, 2021, and the combined environment, explaining 11.96-56.03% of the phenotypic variation. VuANT1 was identified as a causal gene for the QTL qANT5, which regulated anthocyanin content; VuANT1 was highly expressed in immature purple pods but barely detectable in white pods. VuANT1 overexpression in tobacco leaves and yardlong bean hairy roots resulted in purple coloration as a result of anthocyanin accumulation. These findings suggested that VuANT1 was a key regulator of anthocyanin accumulation in yardlong bean. Our results lay a firm foundation for target agricultural trait improvement and clarification of the genetic mechanisms underlying agricultural traits in yardlong bean.

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Hongmei Zhang, Wei Zhang, Shan Meng, Linchong Hui, Xiaoqing Liu, Wei Chen, Wei Yan, Xin Chen, Huatao Chen. Construction of a high-density genetic map for yardlong bean and identification of ANT1 as a regulator of anthocyanin biosynthesis. Horticulture Research, 2024, 11(1): 247 DOI:10.1093/hr/uhad247

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Acknowledgements

This work was supported by the open competition project of seed industry revitalization of Jiangsu Province (JBGS[2021]063), Agriculture Research System of China (CARS–08–G15) and the cooperation program of IUR for Nanjing Agricultural Science & Technology (2023RHCXY Lvhe03).

Author contributions

H.Z., W.Z., and H.C participated in the conception and design of the experiment; H.Z. and W.Z. performed the experiments; W.Z and S.M conducted the phenotypic analysis and wrote the paper; and L.H., X.L., W.C., W.Y., and X.C. revised the manuscript. All authors have read and approved the final version of the manuscript.

Data availability

The data supporting the findings of this work are available within the paper and its supplementary information files. The datasets generated and analysed during this study are available from the corresponding author upon request.

Conflict of interest statement

The authors declare no competing interests.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

Ehlers JD, Hall AE. Cowpea (Vigna unguiculata L. Walp.). Field Crop Res. 1997;53:187-204

[2]

Gondwe TM, Alamu EO, Mdziniso P. et al. Cowpea (Vigna unguicu-lata (L.) Walp) for food security: an evaluation of end-user traits of improved varieties in Swaziland. Sci Rep. 2019;9:15991

[3]

Suanum W, Somta P, Kongjaimun A. et al. Co-localization of QTLs for pod fiber content and pod shattering in F2 and back-cross populations between yardlong bean and wild cowpea. Mol Breeding. 2016;36:80

[4]

Kongjaimun A, Kaga A, Tomooka N. et al. The genetics of domes-tication of yardlong bean, Vigna unguiculata (L.) Walp. Ssp. unguic-ulata cv.-gr. Sesquipedalis. Ann Bot. 2012;109:1185-200

[5]

Xu P, Wu X, Wang B. et al. Development and polymorphism of Vigna unguiculata ssp. unguiculata microsatellite markers used for phylogenetic analysis in asparagus bean (Vigna unguiculata ssp. Mol Breeding. 2010;25:675-84

[6]

Kongjaimun A, Kaga A, Tomooka N. et al. An SSR-based link-age map of yardlong bean (Vigna unguiculata (L.) Walp. Subsp. unguiculata Sesquipedalis group) and QTL analysis of pod length. Genome. 2012;55:81-92

[7]

Matsui T, Ebuchi S, Kobayashi M. et al. Anti-hyperglycemic effect of diacylated anthocyanin derived from Ipomoea batatas culti-var Ayamurasaki can be achieved through the α-glucosidase inhibitory action. J Agric Food Chem. 2002;50:7244-8

[8]

Wang H, Nair MG, Strasburg GM. et al. Antioxidant and antiin-flammatory activities of anthocyanins and their aglycon, cyani-din, from tart cherries. J Nat Prod. 1999;62:294-6

[9]

Yoshimoto M, Okuno S, Yoshinaga M. et al. Antimutagenicity of sweetpotato (Ipomoea batatas) roots. Biosci Biotechnol Biochem. 1999;63:537-41

[10]

Song X, Yang Q, Bai Y. et al. Comprehensive analysis of SSRs and database construction using all complete gene-coding sequences in major horticultural and representative plants. Hortic Res. 2021;8:122

[11]

Kongjaimun A, Somta P, Tomooka N. et al. QTL mapping of pod tenderness and total soluble solid in yardlong bean [Vigna unguiculata (L.) Walp. Subsp. unguiculata cv.-gr. Sesquipedalis]. Euphytica. 2013;189:217-23

[12]

Nakayama M. Flower pigments responsible for cyanic, yellow, and cream-white coloration in carnation. In: Onozaki T, Yagi M, eds. The Carnation Genome. Springer Singapore: Singapore, 2020, 61-79

[13]

Santos-Buelga C, Mateus N, De Freitas V. Anthocyanins. Plant pigments and beyond. J Agric Food Chem. 2014;62:6879-84

[14]

Hu J, Chen G, Zhang Y. et al. Anthocyanin composition and expression analysis of anthocyanin biosynthetic genes in kidney bean pod. Plant Physiol Biochem. 2015;97:304-12

[15]

García-Fernández C, Campa A, Ferreira JJ. Dissecting the genetic control of seed coat color in a RIL population of common bean (Phaseolus vulgaris L.). Theor Appl Genet. 2021;134:3687-98

[16]

García-Fernández C, Campa A, Garzón AS. et al. GWAS of pod morphological and color characters in common bean. BMC Plant Biol. 2021;21:184

[17]

Herniter IA, Muñoz-Amatriaín M, Lo S. et al. Identification of candidate genes controlling black seed coat and pod tip color in cowpea (Vigna unguiculata [L.] Walp). G3 (Bethesda). 2018;8: 3347-55

[18]

Li G, Khan TA, Guo J. et al. Development of SNP-based high-density genetic map and gene mapping of pod colour trait in cowpea (Vigna unguiculata L. Walp.). J Hortic Sci Biotechnol. 2021;96: 87-94

[19]

Byun J, Kim T, Lee J. et al. Identification of CaAN3 as a fruit-specific regulator of anthocyanin biosynthesis in pepper (Cap-sicum annuum). Theor Appl Genet. 2022;135:2197-211

[20]

Erfatpour M, Pauls KP. A R2R3-MYB gene-based marker for the non-darkening seed coat trait in pinto and cranberry beans (Phaseolus vulgaris L.) derived from ‘wit-rood boontje’. Theor Appl Genet. 2020;133:1977-94

[21]

Gonzalez A, Zhao M, Leavitt JM. et al. Regulation of the antho-cyanin biosynthetic pathway by the TTG1/bHLH/Myb transcrip-tional complex in Arabidopsis seedlings. Plant J. 2008;53:814-27

[22]

Lin Y, Laosatit K, Liu J. et al. The mungbean VrP locus encod-ing MYB90, an R2R3-type MYB protein, regulates anthocyanin biosynthesis. Front Plant Sci. 2022;13:895634

[23]

Stracke R, Ishihara H, Huep G. et al. Differential regulation of closely related R2R3-MYB transcription factors controls flavonol accumulation in different parts of the Arabidopsis thaliana seedling. Plant J. 2007;50:660-77

[24]

Wang N, Qu C, Jiang S. et al. The proanthocyanidin-specific transcription factor MdMYBPA1 initiates anthocyanin synthesis under low-temperature conditions in red-fleshed apples. Plant J. 2018;96:39-55

[25]

Muñoz-Amatriaín M, Mirebrahim H, Xu P. et al. Genome resources for climate-resilient cowpea, an essential crop for food security. Plant J. 2017;89:1042-54

[26]

Li Y, Chen Q, Xie X. et al. Integrated metabolomics and tran-scriptomics analyses reveal the molecular mechanisms under-lying the accumulation of anthocyanins and other flavonoids in cowpea pod (Vigna unguiculata L.). J Agric Food Chem. 2020;68: 9260-75

[27]

Pan L, Wang N, Wu Z. et al. A high density genetic map derived from rad sequencing and its application in QTL analysis of yield-related traits in Vigna unguiculata. Front Plant Sci. 2017;8:1544

[28]

Garcia-Oliveira AL, Zate ZZ, Olasanmi B. et al. Genetic dissection of yield associated traits in a cross between cowpea and yard-long bean (Vigna unguiculata (L.) Walp.) based on DArT markers. J Genet. 2020;99:57

[29]

Pan L, Liu M, Kang Y. et al. Comprehensive genomic analyses of Vigna unguiculata provide insights into population differentiation and the genetic basis of key agricultural traits. Plant Biotechnol J. 2023;21:1426-39

[30]

Watcharatpong P, Kaga A, Chen X. et al. Narrowing down a major QTL region conferring pod fiber contents in yardlong bean (Vigna unguiculata), a vegetable cowpea. Genes. 2020;11:363

[31]

Lo S, Muñoz-Amatriaín M, Boukar O. et al. Identification of QTL controlling domestication-related traits in cowpea (Vigna unguiculata L. Walp). Sci Rep. 2018;8:6261

[32]

Xu P, Wu X, Muñoz-Amatriaín M. et al. Genomic regions, cellular components and gene regulatory basis underlying pod length variations in cowpea (V. unguiculata L. Walp). Plant Biotechnol J. 2017;15:547-57

[33]

Iorizzo M, Cavagnaro PF, Bostan H. et al. A cluster of MYB transcription factors regulates anthocyanin biosynthesis in car-rot (Daucus carota L.) root and petiole. Front Plant Sci. 2019;9: 1927

[34]

Paterson AH, Brubaker CL, Wendel JF. A rapid method for extrac-tion of cotton (Gossypium spp.) genomic DNA suitable for RFLP or PCR analysis. Plant Mol Biol Rep. 1993;11:122-7

[35]

Li H, Durbin R. Fast and accurate short read alignment with burrows-wheeler transform. Bioinformatics. 2009;25:1754-60

[36]

Li H, Handsaker B, Wysoker A. et al. The sequence alignment/map format and SAMtools. Bioinformatics. 2009;25:2078-9

[37]

Xie W, Feng Q, Yu H. et al. Parentindependent genotyping for con-structing an ultrahigh-density linkage map based on population sequencing. Proc Natl Acad Sci U S . 2010;107:10578-83

[38]

Wang B, He J, Duan C. et al. Root restriction affects anthocyanin accumulation and composition in berry skin of ‘Kyoho’ grape (Vitis vinifera L. Vitis labrusca L.) during ripening. Sci Horti. 2012;137:20-28

[39]

Rabino I, Mancinelli AL Light, temperature, and anthocyanin production. Plant Physio. 1986;81:922-4

[40]

Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248-54

[41]

Jansen RC, Stam P. High resolution of quantitative traits into multiple loci via interval mapping. Genetics. 1994;136:1447-55

[42]

Zeng ZB. Precision mapping of quantitative trait loci. Genetics. 1994;136:1457-68

[43]

Cui S, He X, Fu S. et al. Genetic dissection of the relationship of apparent biological yield and apparent harvest index with seed yield and yield related traits in soybean. Aust J Agric Re. 2008;59: 86-93

[44]

Kereszt A, Li D, Indrasumunar A. et al. Agrobacterium rhizogenes-mediated transformation of soybean to study root biology. Nat Protoc. 2007;2:948-52

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