The R2R3-type MYB transcription factor MdMYB90-like is responsible for the enhanced skin color of an apple bud sport mutant

Chao Sun , Chunming Wang , Wang Zhang , Shuai Liu , Weiyao Wang , Xinyi Yu , Tao Song , Maxwell Yu , Weichang Yu , Shenchun Qu

Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) : 156

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Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) :156 DOI: 10.1038/s41438-021-00590-3
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The R2R3-type MYB transcription factor MdMYB90-like is responsible for the enhanced skin color of an apple bud sport mutant
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Abstract

The anthocyanin content in apple skin determines its red coloration, as seen in a Fuji apple mutant. Comparative RNA-seq analysis was performed to determine differentially expressed genes at different fruit development stages between the wild-type and the skin color mutant. A novel R2R3-MYB transcription factor, MdMYB90-like, was uncovered as the key regulatory gene for enhanced coloration in the mutant. The expression of MdMYB90-like was 21.3 times higher in the mutant. MdMYB90-like regulates anthocyanin biosynthesis directly through the activation of anthocyanin biosynthesis genes and indirectly through the activation of other transcription factors that activate anthocyanin biosynthesis. MdMYB90-like bound to the promoters of both structural genes (MdCHS and MdUFGT) and other transcription factor genes (MdMYB1 and MdbHLH3) in the yeast one-hybrid system, electrophoretic mobility shift assay, and dual-luciferase assay. Transgenic analysis showed that MdMYB90-like was localized in the nucleus, and its overexpression induced the expression of other anthocyanin-related genes, including MdCHS, MdCHI, MdANS, MdUFGT, MdbHLH3, and MdMYB1. The mutant had reduced levels of DNA methylation in two regions (−1183 to −988 and −2018 to −1778) of the MdMYB90-like gene promoter, which might explain the enhanced expression of the gene and the increased anthocyanin content in the mutant apple skin.

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Chao Sun, Chunming Wang, Wang Zhang, Shuai Liu, Weiyao Wang, Xinyi Yu, Tao Song, Maxwell Yu, Weichang Yu, Shenchun Qu. The R2R3-type MYB transcription factor MdMYB90-like is responsible for the enhanced skin color of an apple bud sport mutant. Horticulture Research, 2021, 8 (1) : 156 DOI:10.1038/s41438-021-00590-3

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References

[1]

Azuma, A. et al. Color recovery in berries of grape (Vitis vinifera L.) ‘Benitaka’, a bud sport of ‘Italia’, is caused by a novel allele at the VvmybA1 locus. Plant Sci. 176, 470-478 (2009).

[2]

Li, P., Zhang, Y., Einhorn, T. C. & Cheng, L. Comparison of phenolic metabolism and primary metabolism between green ‘Anjou’ pear and its bud mutation, red ‘Anjou’. Physiologia Plant. 150, 339-354 (2014).

[3]

Lee, H. S. et al. Analysis of Fuji apple somatic variants from next-generation sequencing. Genet. Mol. Res. 15, 52- 52 (2016).

[4]

Song, C. et al. miRNA and degradome sequencing reveal miRNA and their target genes that may mediate shoot growth in spur type mutant “Yanfu 6”. Front. Plant Sci. 8, 441- 441 (2017).

[5]

El-sharkawy, I., Liang, D. & Xu, K. Transcriptome analysis of an apple (Malus × domestica) yellow fruit somatic mutation identifies a gene network module highly associated with anthocyanin and epigenetic regulation. J. Exp. Bot. 66, 7359-7376 (2015).

[6]

Wang, Z. et al. The methylation of the pcmyb10 promoter is associated with green-skinned sport in max red bartlett pear. Plant Physiol. 162, 885-896 (2013).

[7]

Guo, D. et al. Comparative RNA-Seq profiling of berry development between table grape ‘Kyoho’ and its early-ripening mutant ‘Fengzao’. BMC Genomics 17, 795- 795 (2016).

[8]

Liu, D. et al. Analysis of cuticular wax constituents and genes that contribute to the formation of ‘glossy Newhall’, a spontaneous bud mutant from the wild-type ‘Newhall’ navel orange. Plant Mol. Biol. 88, 573-590 (2015).

[9]

Reuscher, S., Isuzugawa, K., Kawachi, M., Oikawa, A. & Shiratake, K. Comprehensive elemental analysis of fruit flesh from European pear ‘La France’ and its giant fruit bud mutant indicates specific roles for B and Ca in fruit development. Sci. Horticulturae 176, 255-260 (2014).

[10]

Wunsch, A. & Hormaza, J. I. Genetic and molecular analysis in Cristobalina sweet cherry, a spontaneous self-compatible mutant. Sex. Plant Reprod. 17, 203-210 (2004).

[11]

Yang, Y., Yao, G., Yue, W., Zhang, S. & Wu, J. Transcriptome profiling reveals differential gene expression in proanthocyanidin biosynthesis associated with red/green skin color mutant of pear (Pyrus communis L.). Front. Plant Sci. 6, 795- 795 (2015).

[12]

Kang, S. Y., Seeram, N. P., Nair, M. G. & Bourquin, L. D. Tart cherry anthocyanins inhibit tumor development in Apc (Min) mice and reduce proliferation of human colon cancer cells. Cancer Lett. 194, 13-19 (2003).

[13]

Kelebek, H. & Selli, S. Evaluation of chemical constituents and antioxidant activity of sweet cherry (Prunus avium L.) cultivars. Int. J. Food Sci. Technol. 46, 2530-2537 (2011).

[14]

Knekt, P. et al. Dietary flavonoids and the risk of lung cancer and other malignant neoplasms. Am. J. Epidemiol. 146, 223-230 (1997).

[15]

Boyer, J. & Liu, R. H. Apple phytochemicals and their health benefits. Nutr. J. 3, 5 (2004).

[16]

Gerhauser, C. Cancer chemopreventive potential of apples, apple juice, and apple components. Planta Med. 74, 1608-1624 (2008).

[17]

Kondo, S., Hiraoka, K., Kobayashi, S., Honda, C. & Terahara, N. Changes in the expression of anthocyanin biosynthetic genes during apple development. J. Am. Soc. Horticultural Sci. 127, 971-976 (2002).

[18]

Lister, C. E., Lancaster, J. E. & Walker, J. R. L. Developmental changes in enzymes of flavonoid biosynthesis in the skins of red and green apple cultivars. J. Sci. Food Agriculture 71, 313-320 (2015).

[19]

Meng, R. et al. Anthocyanin accumulation and related gene family expression in the skin of dark-grown red and non-red apples (Malus domestica Borkh.) in response to sunlight. Sci. Horticulturae 189, 66-73 (2015).

[20]

Meng, R. et al. Expression profiling of several gene families involved in anthocyanin biosynthesis in apple (Malus domestica Borkh.) skin during fruit development. J. Plant Growth Regul. 35, 449-464 (2016).

[21]

Wang, H., Arakawa, O. & Motomura, Y. Influence of maturity and bagging on the relationship between anthocyanin accumulation and phenylalanine ammonia-lyase (PAL) activity in ‘Jonathan’ apples. Postharvest Biol. Technol. 19, 123-128 (2000).

[22]

Holton, T. A. & Cornish, E. C. Genetics and biochemistry of anthocyanin biosynthesis. Plant Cell 7, 1071-1083 (1995).

[23]

Xie, X., Zhao, J., Hao, Y., Fang, C. & Wang, Y. The ectopic expression of apple MYB1 and bHLH3 differentially activates anthocyanin biosynthesis in tobacco. Plant Cell Tissue Organ Cult. 131, 183-194 (2017).

[24]

Ban, 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. 48, 958-970 (2007).

[25]

Chen, M. et al. SWATH-MS-facilitated proteomic profiling of fruit skin between Fuji apple and a red skin bud sport mutant. BMC Plant Biol. 19, 1-13 (2019).

[26]

Qu, D. et al. Identification of microRNAs and their targets associated with fruit-bagging and subsequent sunlight re-exposure in the “Granny Smith” apple exocarp using high-throughput sequencing. Front. Plant Sci. 7, 27- 27 (2016).

[27]

Treutter, D. Biosynthesis of phenolic compounds and its regulation in apple. Plant Growth Regul. 34, 71-89 (2001).

[28]

Ramsay, N. A. & Glover, B. J. MYB-bHLH-WD40 protein complex and the evolution of cellular diversity. Trends plant Sci. 10, 63-70 (2005).

[29]

Takos, A. M. et al. Light-induced expression of a MYB gene regulates anthocyanin biosynthesis in red apples. Plant Physiol. 142, 1216-1232 (2006).

[30]

Jiang, C., Gu, X. & Peterson, T. Identification of conserved gene structures and carboxy-terminal motifs in the Myb gene family of Arabidopsis and Oryza sativa L. ssp. Indica [J]. Genome Biol. 5, 1-11 (2004).

[31]

Zimmermann, I., Heim, M. A., Weisshaar, B. & Uhrig, J. F. Comprehensive identification of Arabidopsis thaliana MYB transcription factors interacting with R/B‐like BHLH proteins. Plant J. 40, 22-34 (2004).

[32]

Xie, X. et al. The bHLH transcription factor MdbHLH3 promotes anthocyanin accumulation and fruit colouration in response to low temperature in apples. Plant Cell Environ. 35, 1884-1897 (2012).

[33]

Espley, R. V. et al. Multiple repeats of a promoter segment causes transcription factor autoregulation in red apples. Plant Cell 21, 168-183 (2009).

[34]

Xu, Y. et al. Comparison of MdMYB1 sequences and expression of anthocyanin biosynthetic and regulatory genes between Malus domestica Borkh. cultivar ‘Ralls’ and its blushed sport. Euphytica 185, 157-170 (2012).

[35]

Ben-Yehudah, G. et al. Colour accumulation patterns and the anthocyanin biosynthetic pathway in ‘red delicious’ apple variants. J. Horticultural Sci. Biotechnol. 80, 187-192 (2005).

[36]

Shoeva, O. Y., Glagoleva, A. Y. & Khlestkina, E. K. The factors affecting the evolution of the anthocyanin biosynthesis pathway genes in monocot and dicot plant species. BMC Plant Biol. 17, 256 (2017).

[37]

Given, N. K., Venis, M. A. & Grierson, D. Phenylalanine ammonia-lyase activity and anthocyanin synthesis in ripening strawberry fruit. J. Plant Physiol. 133, 25-30 (1988).

[38]

Lister, C. E., Lancaster, J. E. & Walker, J. R. L. Phenylalanine ammonia-lyase (PAL) activity and its relationship to anthocyanin and flavonoid levels in New Zealand-grown apple cultivars. J. Am. Soc. Horticultural Sci. 121, 281-285 (1996).

[39]

Ma, C. et al. Transcriptome profiling reveals transcriptional regulation by DNA methyltransferase inhibitor 5-aza-2′-deoxycytidine enhancing red pigmentation in bagged “Granny Smith” apples (Malus domestica). Int. J. Mol. Sci. 19, 3133 (2018).

[40]

Dare, A. P. et al. Phenotypic changes associated with RNA interference silencing of chalcone synthase in apple (Malus × domestica). Plant J. 74, 398-410 (2013).

[41]

Ban, Y. et al. UDP-sugar biosynthetic pathway: contribution to cyanidin 3-galactoside biosynthesis in apple skin. Planta 230, 871-881 (2009).

[42]

Kobayashi, S., Ishimaru, M., Ding, C. K., Yakushiji, H. & Goto, N. Comparison of UDP-glucose:flavonoid 3-O-glucosyltransferase (UFGT) gene sequences between white grapes (Vitis vinifera) and their sports with red skin. Plant Sci. 160, 543-550 (2001).

[43]

Jaakola, L. New insights into the regulation of anthocyanin biosynthesis in fruits. Trends Plant Sci. 18, 477-483 (2013).

[44]

Jin, H. & Martin, C. Multifunctionality and diversity within the plant MYB-gene family. Plant Mol. Biol. 41, 577-585 (1999).

[45]

Koes, R., Verweij, W. & Quattrocchio, F. Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. Trends Plant Sci. 10, 236-242 (2005).

[46]

Lin-Wang, K. et al. An R2R3 MYB transcription factor associated with regulation of the anthocyanin biosynthetic pathway in Rosaceae. BMC Plant Biol. 10, 50 (2010).

[47]

Espley, R. V. et al. Red colouration in apple fruit is due to the activity of the MYB transcription factor, MdMYB10. Plant J. 49, 414-427 (2007).

[48]

An, J. P. et al. MdWRKY40 promotes wounding-induced anthocyanin biosynthesis in association with MdMYB1 and undergoes MdBT2-mediated degradation. N. Phytologist 224, 380-395 (2019).

[49]

An, J. P. et al. Dynamic regulation of anthocyanin biosynthesis at different light intensities by the BT2-TCP46-MYB1 module in apple. J. Exp. Bot. 71, 3094-3109 (2020).

[50]

An, J. P. et al. EIN3-LIKE1, MYB1, and ETHYLENE RESPONSE FACTOR3 act in a regulatory loop that synergistically modulates ethylene biosynthesis and anthocyanin accumulation. Plant Physiol. 178, 808-823 (2018).

[51]

Telias, A. et al. Apple skin patterning is associated with differential expression of MYB10. BMC Plant Biol. 11, 93-107 (2011).

[52]

Pirie, A. & Mullins, M. G. Changes in anthocyanin and phenolics content of grapevine leaf and fruit tissues treated with sucrose, nitrate, and abscisic acid. Plant Physiol. 58, 468-472 (1976).

[53]

Audic, S. & Claverie, J. The significance of digital gene expression profiles. Genome Res. 7, 986-995 (1997).

[54]

Ye, J. et al. WEGO: a web tool for plotting GO annotations. Nucleic Acids Res. 34, 293-297 (2006).

[55]

Hooper, S. D. & Bork, P. Medusa: a simple tool for interaction graph analysis. Bioinformatics 21, 4432-4433 (2005).

[56]

Livak, K. J. & Schmittgen, T. D. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT Method . Methods 25, 402-408 (2001).

[57]

Li, J. et al. Modulation of BIN2 kinase activity by HY5 controls hypocotyl elongation in the light. Nat. Commun. 11, 1 (2020).

[58]

Hajdukiewicz, P. T., Svab, Z. & Maliga, P. The small, versatile pPZP family of Agrobacterium binary vectors for plant transformation. Plant Mol. Biol. 25, 989-994 (1994).

[59]

An, J. et al. The bZIP transcription factor MdHY5 regulates anthocyanin accumulation and nitrate assimilation in apple. Horticulture Res. 4, 17023 (2017).

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