Construction of a high-density genetic map based on specific-locus amplified fragment sequencing and identification of loci controlling anthocyanin pigmentation in Yunnan red radish

Jing Tao , Shikai Li , Qian Wang , Yi Yuan , Jiqiong Ma , Minghui Xu , Yi Yang , Cui Zhang , Lijuan Chen , Yiding Sun

Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) : uhab031

PDF (1746KB)
Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) :uhab031 DOI: 10.1093/hr/uhab031
Article
research-article
Construction of a high-density genetic map based on specific-locus amplified fragment sequencing and identification of loci controlling anthocyanin pigmentation in Yunnan red radish
Author information +
History +
PDF (1746KB)

Abstract

Radish (Raphanus sativus L.) belongs to the family Brassicaceae. The Yunnan red radish variety contains relatively large amounts of anthocyanins, making them important raw materials for producing edible red pigment. However, the genetic mechanism underlying this pigmentation has not been fully characterized. Here, the radish inbred line YAAS-WR1 (white root skin and white root flesh) was crossed with the inbred line YAAS-RR1 (red root skin and red root flesh) to produce F1 , F>2 , BC>1 P1 , and BC1 P2 populations. Genetic analyses revealed that the pigmented/non-pigmented and purple/red traits were controlled by two genetic loci. The F2 population and the specific-locus amplified fragment sequencing (SLAF-seq) technique were used to construct a high-density genetic map (1230.16 cM), which contained 4032 markers distributed in nine linkage groups, with a mean distance between markers of 0.31 cM. Additionally, two quantitative trait loci (QAC1 and QAC2) considerably affecting radish pigmentation were detected. A bioinformatics analysis of the QAC1 region identified 58 predicted protein-coding genes. Of these, RsF3 H , which is related to anthocyanin biosynthesis, was revealed as a likely candidate gene responsible for the purple/red trait. The results were further verified by analyzing gene structure and expression. Regarding QAC2, RsMYB1.3 was determined to be a likely candidate gene important for the pigmented/non-pigmented trait, with a 4-bp insertion in the first exon that introduced a premature termination codon in the YAAS-WR1 sequence. Assays demonstrated that RsMYB1.3 interacted with RsTT8 and activated RsTT8 and RsUFGT expression . These findings may help clarify the complex regulatory mechanism underlying radish anthocyanin synthesis. Furthermore, this study’s results may be relevant for the molecular breeding of radish to improve the anthocyanin content and appearance of the taproots.

Cite this article

Download citation ▾
Jing Tao, Shikai Li, Qian Wang, Yi Yuan, Jiqiong Ma, Minghui Xu, Yi Yang, Cui Zhang, Lijuan Chen, Yiding Sun. Construction of a high-density genetic map based on specific-locus amplified fragment sequencing and identification of loci controlling anthocyanin pigmentation in Yunnan red radish. Horticulture Research, 2022, 9 (1) : uhab031 DOI:10.1093/hr/uhab031

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Landi M, Tattini M, Gould KS . Multiple functional roles of anthocyanins in plant-environment interactions. Environ Exp Bot. 2015; 119: 4-17.

[2]

Dao TTH, Linthorst HJM, Verpoorte R . Chalcone synthase and its functions in plant resistance. Phytochem Rev. 2011; 10: 397-412.

[3]

Liang J, He J . Protective role of anthocyanins in plants under low nitrogen stress. Biochem Biophys Res Commun. 2018; 498: 946-53.

[4]

He J, Giusti MM . Anthocyanins: natural colorants with health promoting properties. Annu Rev Food Sci Technol. 2010; 1: 163-87.

[5]

Nabavi SF, Habtemariam S, Daglia M et al. Anthocyanins as a potential therapy for diabetic retinopathy. Curr Med Chem. 2015; 22: 51-8.

[6]

Bendokas V, Stanys V, Mažeikien I et al. Anthocyanins: from the field to the antioxidants in the body. Antioxidants (Basel). 2020; 9: 819.

[7]

Shi MZ, Xie DY . Biosynthesis and metabolic engineering of anthocyanins in Arabidopsis thaliana . Recent Pat Biotechnol. 2014; 8: 47-60.

[8]

Holton TA, Cornish EC . Genetics and biochemistry of anthocyanin biosynthesis. Plant Cell. 1995; 7: 1071-83.

[9]

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

[10]

Dong W, Niu L, Gu J et al. Isolation of a WD40-repeat gene regulating anthocyanin biosynthesis in storage roots of purple-fleshed sweet potato. Acta Physiol Plant. 2014; 36: 1123-32.

[11]

Qi T, Song S, Ren Q et al. The jasmonate-ZIM-domain proteins interact with the WD-repeat/bHLH/MYB complexes to regulate jasmonate-mediated anthocyanin accumulation and trichome initiation in Arabidopsis thaliana . Plant Cell. 2011; 23: 1795-814.

[12]

Gou JY, Felippes FF, Liu CJ et al. Negative regulation of anthocyanin biosynthesis in Arabidopsis by a miR156-targeted SPL transcription factor . Plant Cell. 2011; 23: 1512-22.

[13]

Zhou H, Lin-Wang K, Wang HL et al. Molecular genetics of blood-fleshed peach reveals activation of anthocyanin biosynthesis by NAC transcription factors. Plant J. 2015; 82: 105-21.

[14]

Zhou LM, Zheng KJ, Wang XY et al. Control of trichome formation in Arabidopsis by poplar single-repeat R3 MYB transcription factors. Front Plant Sci. 2014; 5: 262.

[15]

Nemie-Feyissa D, Olafsdottir SM, Heidari B et al. Nitrogen depletion and small R3-MYB transcription factors affecting anthocyanin accumulation in Arabidopsis leaves. Phytochemistry. 2014; 98: 34-40.

[16]

Cao X, Qiu Z, Wang X et al. A putative R3 MYB repressor is the candidate gene underlying atroviolacium, a locus for anthocyanin pigmentation in tomato fruit. J Exp Bot. 2017; 68: 5745-58.

[17]

Xu XW, Lu L, Zhu BY et al. QTL mapping of cucumber fruit flesh thickness by SLAF-seq. Sci Rep. 2015; 5: 15829.

[18]

Gao J, Peng H, Chen F et al. Genome-wide analysis of transcription factors related to anthocyanin biosynthesis in carmine radish (Raphanus sativus L.) fleshy roots . PeerJ. 2019; 7: e8041.

[19]

Wang Y, Pan Y, Liu Z et al. De novo transcriptome sequencing of radish (Raphanus sativus L.) and analysis of major genes involved in glucosinolate metabolism . BMC Genomics. 2013; 14: 836.

[20]

Manivannan A, Kim JH, Kim DS et al. Deciphering the nutraceutical potential of Raphanus sativus - a comprehensive overview. Nutrients. 2019; 11: 402.

[21]

Tao J, Wang Q, Yuan Y et al. Relationship between main agronomic traits and pigment yield of Yunnan red radish. Chinese Agric Sci Bull. 2019; 35: 59-63.

[22]

Su NN, Lu YW, Wu Q et al. UV-B-induced anthocyanin accumulation in hypocotyls of radish sprouts continues in the dark after irradiation. J Sci Food Agric. 2016; 96: 886-92.

[23]

Meng ZN, He QW, Lang FQ et al. Developmental changes of distribution of chromogen in varieties of garden radish (Raphanus sativus L.) . J Shandong Univ. 2000; 35: 224-9.

[24]

Lu FS, Tan GX, Luo YT et al. Preliminary study of pigment distribution pattern on red-core radish. Southwest China J Agric Sci. 2006; 19: 276-9.

[25]

Park NI, Xu H, Li X et al. Anthocyanin accumulation and expression of anthocyanin biosynthetic genes in radish (Raphanus sativus) . J Agric Food Chem. 2011; 59: 6034-9.

[26]

Muleke EM, Fan L, Wang Y . Coordinated regulation of anthocyanin biosynthesis genes confers varied phenotypic and spatial-temporal anthocyanin accumulation in radish (Raphanus sativus L.) . Front Plant Sci. 2017; 8: 1243.

[27]

Sun YY, Wang JL, Qiu Y et al. Identification of ‘Xinlimei’ radish candidate genes associated with anthocyanin biosynthesis based on a transcriptome analysis. Gene. 2018; 657: 81-91.

[28]

Liu TJ, Wang JL, Wu CH et al. Combined QTL-Seq and traditional linkage analysis to identify candidate genes for purple skin of radish fleshy taproots. Front Genet. 2019; 10: 808.

[29]

Lim SH, Song JH, Kim DH . Activation of anthocyanin biosynthesis by expression of the radish R2R3-MYB transcription factor gene RsMYB1 . Plant Cell Rep. 2016; 35: 641-53.

[30]

Lim SH, Kim DH, Kim JK . A radish basic helix-loop-helix transcription factor, RsTT8 acts a positive regulator for anthocyanin biosynthesis. Front Plant Sci. 2017; 8: 1917.

[31]

Luo XB, Xu L, Wang Y et al. An ultrahigh density genetic map provides insights into genome synteny, recombination landscape and taproot skin color in radish (Raphanus sativus L.) . Plant Biotechnol. 2019; 18: 274-86.

[32]

Lai B, Cheng YY, Liu H et al. Differential anthocyanin accumulation in radish taproot: importance of RsMYB1 gene structure. Plant Cell Rep. 2020; 39: 217-26.

[33]

Sun XW, Liu DY, Zhang XF et al. SLAF-seq: an efficient method of large-scale de novo SNP discovery and genotyping using high-throughput sequencing. PLoS One. 2013; 8: e58700.

[34]

Xu X, Xu R, Zhu B et al. A high-density genetic map of cucumber derived from specific length amplified fragment sequencing (SLAF-seq). Front Plant Sci. 2014; 5: 768.

[35]

Zheng YT, Xu F, Li QK et al. QTL mapping combined with bulked segregant analysis identify SNP markers linked to leaf shape traits in Pisum sativum using SLAF sequencing. Front Genet. 2018; 9: 615.

[36]

Li GH, Chen HC, Liu JL et al. A high-density genetic map developed by specific-locus amplified fragment (SLAF) sequencing and identification of a locus controlling anthocyanin pigmentation in stalk of zicaitai (Brassica rapa L. ssp. chinensis var. purpurea) . BMC Genomics. 2019; 20: 343.

[37]

Yu HF, Wang JS, Zhao ZQ et al. Construction of a high-density genetic map and identification of loci related to hollow stem trait in broccoli (Brassica oleracea L. italica) . Front Plant Sci. 2019; 10: 45.

[38]

Chu H, Jeong JC, Kim WJ et al. Expression of the sweet potato R2R3-type IbMYB1a gene induces anthocyanin accumulation in Arabidopsis . Physiol Plant. 2013; 148: 189-99.

[39]

Doyle J, Doyle J . Genomic plant DNA preparation from fresh tissue. Phytochem Bull. 1987; 19: 11-5.

[40]

Untergasser A, Cutcutache I, Koressaar T et al. Primer3 - new capabilities and interfaces. Nucleic Acids Res. 2012; 40: e115.

[41]

Masukawa T, Cheon KS, Mizuta D et al. Insertion of a retrotransposon into a flavonoid 30-hydroxylase homolog confers the red root character in the radish (Raphanus sativus L. var. longipinnatus L. H. Bailey) . Hortic J. 2018; 87: 89-96.

[42]

Kitashiba H, Li F, Hirakawa H et al. Draft sequences of the radish (Raphanus sativus L.) genome . DNA Res. 2014; 21: 481-90.

[43]

Mun JH, Chung H, Chung WH et al. Construction of a reference genetic map of Raphanus sativus based on genotyping by whole-genome resequencing. Theor Appl Genet. 2015; 128: 259-72.

[44]

Xu L, Wang LJ, Gong YQ et al. Genetic linkage map construction and QTL mapping of cadmium accumulation in radish (Raphanus sativus L.) . Theor Appl Genet. 2012; 125: 659-70.

[45]

Frost HB . Heterosis and dominance of size factors in Raphanus . Genetics. 1923; 8: 116-53.

[46]

Uphof JC . On Mendelian factors in radishes. Genetics. 1924; 9: 292-304.

[47]

Hoshi T, Takemura E, Hayashi K . Genetic modification of hydroxylation pattern in radish anthocyanins. Studies on anthocyanins, XLII. Bot Mag Tokyo. 1963; 76: 431-9.

[48]

Masukawa T, Cheon KS, Mizuta D et al. Development of mutant RsF30H allele-based marker for selection of purple and red root in radish (Raphanus sativus L. var. longipinnatus L. H. Bailey) . Euphytica. 2019; 215: 119.

[49]

Yi G, Kim JS, Park JE et al. MYB1 transcription factor is a candidate responsible for red root skin in radish (Raphanus sativus L.) . PLoS One. 2018; 13: e0204241.

[50]

Allan AC, Hellens RP, Laing WA . MYB transcription factors that colour our fruit. Trends Plant Sci. 2008; 13: 99-102.

[51]

Kobayashi S, Goto-Yamamoto N, Hirochika H . Retrotransposon-induced mutations in grape skin color. Science. 2004; 304: 982.

[52]

Zhang L, Hu J, Han X et al. A high-quality apple genome assembly reveals the association of a retrotransposon and red fruit colour. Nat Commun. 2019; 10: 1494.

[53]

Takos AM, Jaffe FW, Jacob SR et al. Light-induced expression of a MYB gene regulates anthocyanin biosynthesis in red apples. Plant Physiol. 2006; 142: 1216-32.

[54]

Ban Y, Honda C, Hatsuyama Y et al. Isolation and functional analysis of a MYB transcription factor gene that is a key regulator for the development of red coloration in apple skin. Plant Cell Physiol. 2007; 48: 958-70.

[55]

Espley RV, Hellens RP, Putterill J et al. Red colouration in apple fruit is due to the activity of the MYB transcription factor, MdMYB10 . Plant J. 2007; 49: 414-27.

[56]

Zhang YJ, Hu ZL, Chu GH et al. Anthocyanin accumulation and molecular analysis of anthocyanin biosynthesis-associated genes in eggplant (Solanum melongena L.) . J Agric Food Chem. 2014; 62: 2906-12.

[57]

Chiu LW, Zhou X, Burke S et al. The purple cauliflower arises from activation of a MYB transcription factor. Plant Physiol. 2010; 154: 1470-80.

[58]

Chiu LW, Li L . Characterization of the regulatory network of BoMYB2 in controlling anthocyanin biosynthesis in purple cauliflower. Planta. 2012; 236: 1153-64.

[59]

He Q, Wu JQ, Xue YH et al. The novel gene BrMYB2, located on chromosome A07, with a short intron 1 controls the purple-head trait of Chinese cabbage (Brassica rapa L.) . Hortic Res 2020; 7: 97.

[60]

Fan LX, Wang Y, Xu L et al. A genome-wide association study uncovers a critical role of the RsPAP2 gene in red-skinned Raphanus sativus L. Hortic Res 2020; 7: 164.

[61]

Wang QB, Wang YP, Sun HH et al. Transposon-induced methylation of the RsMYB1 promoter might be associated with the production of white-fleshed mutants. J Exp Biol. 2020; 71: 2537-50.

[62]

Harborne JB, Paxman GJ . Genetics of anthocyanin product in the radish. Heredity. 2011; 19: 505-6.

PDF (1746KB)

37

Accesses

0

Citation

Detail

Sections
Recommended

/