Published September 30, 2021
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Genome-wide identification and characterization of genes involved in melatonin biosynthesis in Morus notabilis (wild mulberry)
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- 1. * & State Key Laboratory of Silkworm Genome Biology, Key Laboratory of Sericultural Biology and Genetic Breeding, Ministry of Agriculture, Southwest University,
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Zheng, Sha, Zhu, Yingxue, Liu, Changying, Fan, Wei, Xiang, Zhonghuai, Zhao, Aichun (2021): Genome-wide identification and characterization of genes involved in melatonin biosynthesis in Morus notabilis (wild mulberry). Phytochemistry (112819) 189: 1-12, DOI: 10.1016/j.phytochem.2021.112819, URL: http://dx.doi.org/10.1016/j.phytochem.2021.112819
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References
- Aghdam, M.S., Luo, Z., Li, L., Jannatizadeh, A., Fard, J.R., Pirzad, F., 2020. Melatonin treatment maintains nutraceutical properties of pomegranate fruits during cold storage. Food Chem. 303 https://doi.org/10.1016/j.foodchem.2019.125385, 125385.125381-125385.125387.
- Arnao, M.B., Hern´andez-Ruiz, J., 2020. Is phytomelatonin a new plant hormone? Agronomy 10, 95. https://doi.org/10.3390/agronomy10010095.
- Back, K., Tan, D.X., Reiter, R.J., 2016. Melatonin biosynthesis in plants: multiple pathways catalyze tryptophan to melatonin in the cytoplasm or chloroplasts. J. Pineal Res. 61, 426-437. https://doi.org/10.1111/jpi.12364.
- Bhattacharjee, A., 2018. Phytomelatonin: a comprehensive literature review and recent advance on medicinal meadow. International Journal of Hydrology 2. https://doi. org/10.15406/ijh.2018.02.00102.
- Bixiao, Z., Xiaodong, Z., Pingli, H., Lin, W., Qiong, L., Chao, F., Jingzhe, Z., Qingtian, L., Zhenhai, H., Jin, K., 2015. Overexpression of MzASMT improves melatonin production and enhances drought tolerance in transgenic Arabidopsis thaliana plants. J. Pineal Res. 57, 408-417. https://doi.org/10.1111/jpi.12180.
- Brainard, G.C., Hanifin, J.P., Greeson, J.M., Byrne, B., Glickman, G., Gerner, E., Rollag, M.D., 2001. Action spectrum for melatonin regulation in humans: evidence for a novel circadian photoreceptor. J. Neurosci. 6405-6412. https://doi.org/ 10.1162/08989290152541494.
- Byeon, Y., Lee, H.J., Lee, H.Y., Back, K., 2016. Cloning and functional characterization of the Arabidopsis N-acetylserotonin O-methyltransferase responsible for melatonin synthesis. J. Pineal Res. 60, 65-73. https://doi.org/10.1111/jpi.12289.
- Byeon, Y., Lee, H.Y., Choi, D.-W., Back, K., 2015. Chloroplast-encoded serotonin Nacetyltransferase in the red alga Pyropia yezoensis: gene transition to the nucleus from chloroplasts. J. Exp. Bot. 66, 709-717. https://doi.org/10.1093/jxb/eru357.
- Byeon, Y., Lee, H.Y., Lee, K., Back, K., 2014a. Caffeic acid O -methyltransferase is involved in the synthesis of melatonin by methylating N -acetylserotonin in Arabidopsis. J. Pineal Res. 57, 219-227. https://doi.org/10.1111/jpi.12160.
- Byeon, Y., Lee, K., Park, Y.-I., Park, S., Back, K., 2013. Molecular cloning and functional analysis of serotonin N-acetyltransferase from the cyanobacterium Synechocystis sp. PCC 6803. J. Pineal Res. 55, 371-376. https://doi.org/10.1111/jpi.12080.
- Byeon, Y., Park, S., Lee, H.Y., Kim, Y.-S., Back, K., 2014b. Elevated production of melatonin in transgenic rice seeds expressing rice tryptophan decarboxylase. J. Pineal Res. 56, 275-282. https://doi.org/10.1111/jpi.12120.
- Champney, T.H., Holtorf, A.P., Steger, R.W., Reiter, R.J., 1984. Concurrent determination of enzymatic activities and substrate concentrations in the melatonin synthetic pathway within the same rat pineal gland. Journal of Neuroence Research 11, 59-66. https://doi.org/10.1002/jnr.490110107.
- Chen, G., Huo, Y., Tan, D.-X., Liang, Z., Zhang, W., Zhang, Y., 2003. Melatonin in Chinese medicinal herbs. Life Sci. 73, 19-26. https://doi.org/10.1016/s0024-3205(03) 00252-2.
- Choi, G.H., Lee, H.Y., Back, K., 2017. Chloroplast overexpression of rice caffeic acid Omethyltransferase increases melatonin production in chloroplasts via the 5- methoxytryptamine pathway in transgenic rice plants. J. Pineal Res. 63, e12412 https://doi.org/10.1111/jpi.12412.
- Dollins, A.B., Zhdanova, I.V., Wurtman, R.J., Lynch, H.J., Deng, M.H., 1994. Effect of inducing nocturnal serum melatonin concentrations in daytime on sleep, mood, body temperature, and performance. Proc. Natl. Acad. Sci. U.S.A. 91, 1824-1828, 10.2307/2364029.
- Dubbels, R., Reiter, R.J., Klenke, E., Goebel, A., Schnakenberg, E., Ehlers, C., Schiwara, H.W., Schloot, W., 1995. Melatonin in edible plants identified by radioimmunoassay and by high performance liquid chromatography-mass spectrometry. J. Pineal Res. 18, 28-31. https://doi.org/10.1111/j.1600-079x.1995. tb00136.x.
- Dun-Xian, T., Manchester, L.C., Xiaoyan, L., Rosales-Corral, S.A., Dario, A.C., Reiter, R.J., 2013. Mitochondria and chloroplasts as the original sites of melatonin synthesis: a hypothesis related to melatonin' s primary function and evolution in eukaryotes. J. Pineal Res. 54, 127-138. https://doi.org/10.1111/jpi.12026.
- Facchini, P.J., Huber-Allanach, K.L., Tari, L.W., 2000. Plant aromatic L-amino acid decarboxylases: evolution, biochemistry, regulation, and metabolic engineering applications. Phytochemistry 54, 121-138. https://doi.org/10.1016/s0031-9422 (00)00050-9.
- Fan, W., Liu, C.Y., Cao, B.N., Qin, M.L., Long, D.P., Xiang, Z.H., Zhao, A.C., 2018. Genome-wide identification and characterization of four gene families putatively involved in cadmium uptake, translocation and sequestration in mulberry. Front. Plant Sci. 9, 879. https://doi.org/10.3389/fpls.2018.00879.
- Fujiwara, T., Maisonneuve, S.M., Mizutani, M., Chen, L., Wong, H.L., Kawasaki, T., Shimamoto, K., 2010. Sekiguchi lesion gene encodes a cytochrome P450 monooxygenase that catalyzes conversion of tryptamine to serotonin in rice. J. Biol. Chem. 285, 11308-11313. https://doi.org/10.1074/jbc.M109.091371.
- Ganguly, S., Mummaneni, P., Steinbach, P.J., Klein, D.C., Coon, S.L., 2001. Characterization of the Saccharomyces cerevisiae homolog of the melatonin rhythm enzyme arylalkylamine N-acetyltransferase (EC 2.3.1.87). J. Biol. Chem. 276, 47239-47247. https://doi.org/10.1074/jbc.M107222200.
- Gibson, R.A., Barrett, G., Wightman, F., 1972. Biosynthesis and metabolism of indol-3ylacetic acid: III. Partial purification and properties of a tryptamine-forming l-tryptophan dbcarboxylase from tomato shoots. J. Exp. Bot. 23, 775-786. https://doi. org/10.1093/jxb/23.3.775.
- Hanukoglu, I., 1996. Electron transfer proteins of cytochrome P450 systems. Adv. Mol. Cell. Biol. 14, 29-56. https://doi.org/10.1016/S1569-2558(08)60339-2.
- Hattori, A., Migitaka, H., Iigo, M., Itoh, M., Yamamoto, K., Ohtanikaneko, R., Hara, M., Suzuki, T., Reiter, R.J., 1995. Identification of melatonin in plants and its effects on plasma melatonin levels and binding to melatonin receptors in vertebrates. Biochem. Mol. Biol. Int. 35, 627-634. PMID: 7773197.
- Ichihara, N., Okada, M., Takeda, M., 2002. Characterization and purification of polymorphic arylalkylamine N-acetyltransferase from the American cockroach, Periplaneta americana. Insect Biochem. Mol. Biol. 32, 15-22. https://doi.org/ 10.1016/S0965-1748(01)00075-3.
- Kang, K., Kong, K., Park, S., Natsagdorj, U., Kim, Y.S., Back, K., 2011. Molecular cloning of a plant N-acetylserotonin methyltransferase and its expression characteristics in rice. J. Pineal Res. 50, 304-309. https://doi.org/10.1111/j.1600-079x.2010.00841. x.
- Kang, K., Lee, K., Park, S., Byeon, Y., Back, K., 2013. Molecular cloning of rice serotonin N-acetyltransferase, the penultimate gene in plant melatonin biosynthesis. J. Pineal Res. 55, 7-13. https://doi.org/10.1111/jpi.12011.
- Kang, K., Lee, K., Park, S., Kim, Y.S., Back, K., 2010. Enhanced production of melatonin by ectopic overexpression of human serotonin N-acetyltransferase plays a role in cold resistance in transgenic rice seedlings. J. Pineal Res. 49, 176-182. https://doi. org/10.1111/j.1600-079x.2010.00783.x.
- Kang, S., Kang, K., Lee, K., Back, K., 2007a. Characterization of rice tryptophan decarboxylases and their direct involvement in serotonin biosynthesis in transgenic rice. Planta 227, 263-272. https://doi.org/10.1007/s00425-007-0614-z.
- Kang, S., Kang, K., Lee, K., Back, K., 2007b. Characterization of tryptamine 5-hydroxylase and serotonin synthesis in rice plants. Plant Cell Rep. 26, 2009-2015. https:// doi.org/10.1007/s00299-007-0405-9.
- Ke, Q., Ye, J., Wang, B., Ren, J., Yin, L., Deng, X., Wang, S., 2018. Melatonin mitigates salt stress in wheat seedlings by modulating polyamine metabolism. Front. Plant Sci. 9, 914. https://doi.org/10.3389/fpls.2018.00914.
- Lee, H.Y., Byeon, Y., Lee, K., Lee, H.-J., Back, K., 2014. Cloning of Arabidopsis serotonin N-acetyltransferase and its role with caffeic acid O-methyltransferase in the biosynthesis of melatonin in vitro despite their different subcellular localizations. J. Pineal Res. 57, 418-426. https://doi.org/10.1111/jpi.12181.
- Lerner, A.B., Case, J.D., Takahashi, Y., Lee, T.H., Mori, W., 1958. Isolation of melatonin, a pineal factor that lightens melanocytes. J. Am. Chem. Soc. 80 https://doi.org/ 10.1021/ja01543a060.
- Lewis, D.F.V., Watson, E., Lake, B.G., 1998. Evolution of the cytochrome P450 superfamily: sequence alignments and pharmacogenetics. Mutat. Res. Rev. Mutat. Res. 410, 245-270. https://doi.org/10.1016/S1383-5742(97)00040-9.
- Lewy, A.J., Ahmed, S., Jackson, J.M., Sack, R.L., 1992. Melatonin shifts human circadian rhythms according to a phase-response curve. Chronobiol. Int. 9, 380-392. https:// doi.org/10.3109/07420529209064550.
- Li, L., 2016. Molecular cloning and characterization of two genes encoding tryptophan decarboxylase from aegilops variabilis with resistance to the cereal cyst nematode (Heterodera avenae) and root-knot nematode (Meloidogyne naasi). Plant Mol. Biol. Rep. 34, 273-282. https://doi.org/10.1007/s11105-015-0909-3.
- Lieberman, H.R., Waldhauser, F., Garfield, G., Lynch, H.J., Wurtman, R.J., 1984. Effects of melatonin on human mood and performance. Brain Res. 323, 201-207. https:// doi.org/10.1016/0006-8993(84)90290-7.
- Liu, D., Meng, S., Xiang, Z., He, N., Yang, G., 2019. Antimicrobial mechanism of reaction products of Morus notabilis (mulberry) polyphenol oxidases and chlorogenic acid. Phytochemistry 163, 1-10. https://doi.org/10.1016/j.phytochem.2019.03.026.
- Manchester, L.C., Coto-Montes, A., Boga, J.A., Andersen, L.P.H., Zhou, Z., Galano, A., Vriend, J., Tan, D.X., Reiter, R.J., 2015. Melatonin: an ancient molecule that makes oxygen metabolically tolerable. J. Pineal Res. 59, 403-419. https://doi.org/ 10.1111/jpi.12267.
- Nakatsubo, T., Kitamura, Y., Sakakibara, N., Mizutani, M., Hattori, T., Sakurai, N., Shibata, D., Suzuki, S., Umezawa, T., 2008. At5g54160 gene encodes Arabidopsis thaliana 5-hydroxyconiferaldehyde O -methyltransferase. J. Wood Sci. 54, 312-317. https://doi.org/10.1007/s10086-008-0958-4.
- Nawaz, M.A., Huang, Y., Bie, Z., Ahmed, W., Reiter, R.J., Niu, M., Hameed, S., 2016. Melatonin: current status and future perspectives in plant science. Front. Plant Sci. 6, 1230. https://doi.org/10.3389/fpls.2015.01230.
- Pan, L., Zheng, J., Liu, J., Guo, J., Liu, F., Liu, L., Wan, H., 2019. Analysis of the ASMT gene family in pepper (capsicum annuum L.): identification, phylogeny, and expression profiles. Int J Genomics 2019, 7241096. https://doi.org/10.1155/2019/ 7241096.
- Park, S., Byeon, Y., Back, K., 2013. Transcriptional suppression of tryptamine 5-hydroxylase, a terminal serotonin biosynthetic gene, induces melatonin biosynthesis in rice (Oryza sativa L.). J. Pineal Res. 55, 131-137. https://doi.org/10.1111/ jpi.12053.
- Park, S., Byeon, Y., Lee, H.Y., Kim, Y.S., Ahn, T., Back, K., 2014. Cloning and characterization of a serotonin N -acetyltransferase from a gymnosperm, loblolly pine ( Pinus taeda ). J. Pineal Res. 57, 348-355. https://doi.org/10.1111/jpi.12174.
- Pothinuch, P., Tongchitpakdee, S., 2011. Melatonin contents in mulberry (Morus spp.) leaves: effects of sample preparation, cultivar, leaf age and tea processing. Food Chem. 128, 415-419. https://doi.org/10.1016/j.foodchem.2011.03.045.
- Rudiger, H., 2016. Melatonin in plants - diversity of levels and multiplicity of functions. Frontiers in Plant ence 7, 198. https://doi.org/10.3389/fpls.2016.00198.
- Reiter, R.J., Mayo, J.C., Tan, D.X., Sainz, R.M., Alatorre-Jimenez, M., Qin, L., 2016. Melatonin as an antioxidant: under promises but over delivers. J. Pineal Res. 61, 253-278. https://doi.org/10.1111/jpi.12360.
- Reiter, R.J., Tan, D.X., Rosalescorral, S., Manchester, L.C., 2013. The universal nature, unequal distribution and antioxidant functions of melatonin and its derivatives. Mini Rev. Med. Chem. 13, 373-384. https://doi.org/10.2174/138955713804999810.
- Rodriguez, C., Mayo, J.C., Sainz, R.M., Antolin, I., Reiter, R.J., 2010. Regulation of antioxidant enzymes: a significant role for melatonin. J. Pineal Res. 36, 1-9. https:// doi.org/10.1046/j.1600-079x.2003.00092.x.
- Sangkyu, Park, Kiyoon, Kang, Shin, Woo, Lee, Mi-Jeong, Ahn, Jung-Myung, 2011. Production of serotonin by dual expression of tryptophan decarboxylase and tryptamine 5-hydroxylase in Escherichia coli. Appl. Microbiol. Biotechnol. 89, 1387-1394. https://doi.org/10.1007/s00253-010-2994-4.
- Sangkyu, P., Yeong, B., Kyoungwhan, B., 2013. Functional analyses of three ASMT gene family members in rice plants. J. Pineal Res. 55, 409-415. https://doi.org/10.1111/ jpi.12088.
- Sprenger, J., Hardeland, R., Fuhrberg, B., Han, S.Z., 1999. Melatonin and other 5- methoxylated indoles in yeast : presence in high concentrations and dependence on tryptophan availability. Cytologia 64, 209-213. https://doi.org/10.1508/ cytologia.64.209.
- Tan, D., Hardeland, R., Back, K., Manchester, L.C., Alatorre-Jimenez, M., Reiter, R.J., 2016. On the significance of an alternate pathway of melatonin synthesis via 5- methoxytryptamine: comparisons across species. J. Pineal Res. 61, 27-40. https:// doi.org/10.1111/jpi.12336.
- Tan, D.X., Reiter, R.J., 2020. An evolutionary view of melatonin synthesis and metabolism related to its biological functions in plants. J. Exp. Bot. 71235 https:// doi.org/10.1093/jxb/eraa235.
- Ud-Din, A.I.M.S., Tikhomirova, A., 2016. Molecular sciences structure and functional diversity of GCN5-related N-acetyltransferases (GNAT). International Journal of Molecular ences 17, 1018. https://doi.org/10.3390/ijms17071018.
- Wang, C., Yin, L.Y., Shi, X.Y., Xiao, H., Kang, K., Liu, X.Y., Zhan, J.C., Huang, W.D., 2016. Effect of cultivar, temperature, and environmental conditions on the dynamic change of melatonin in mulberry fruit development and wine fermentation. J. Food Sci. 81, M958-M967. https://doi.org/10.1111/1750-3841.13263.
- Weicheng, L., Dake, Z., Chunfang, Z., Chen, C., Xin, P., Yuan, C., Hongjian, W., 2017. Genomic analysis of the ASMT gene family in Solanum lycopersicum. Molecules 22, 1984. https://doi.org/10.3390/molecules22111984.
- Xin, P., Yanping, W., Yuan, C., Luzhao, P., Qingjing, Y., Rongqing, W., Meiying, R., Guozhi, Z., Zhuping, Y., Zhimiao, L., 2018. The tryptophan decarboxylase in Solanum lycopersicum. Molecules 23, 998. https://doi.org/10.3390/ molecules23050998.
- Yamazaki, Y., 2003. Camptothecin biosynthetic genes in hairy roots of Ophiorrhiza pumila: cloning, characterization and differential expression in tissues and by stress compounds. Plant Cell Physiol. 44, 395-403. https://doi.org/10.1093/pcp/pcg051.
- Yeong, B., Hyoung Yool, L., Kyungjin, L., Sangkyu, P., Kyoungwhan, B., 2013. Cellular localization and kinetics of the rice melatonin biosynthetic enzymes SNAT and ASMT. J. Pineal Res. 56, 107-114. https://doi.org/10.1111/jpi.12103.
- Yeong Byeon, G.-H.C., , Hyoung Yool Lee, Back, Kyoungwhan, 2015. Melatonin biosynthesis requires N-acetylserotonin methyltransferase activity of caffeic acid Omethyltransferase in rice. J. Exp. Bot. 66, 6917-6925. https://doi.org/10.1093/jxb/ erv396.
- Zhan, H., Nie, X., Zhang, T., Li, S., Wang, X., Du, X., Tong, W., Song, W., 2019. Melatonin: a small molecule but important for salt stress tolerance in plants. Int. J. Mol. Sci. 20, 709. https://doi.org/10.3390/ijms20030709.
- Zhang, N., Sun, Q., Zhang, H., Cao, Y., Weeda, S., Ren, S., Guo, Y.D., 2015. Roles of melatonin in abiotic stress resistance in plants. J. Exp. Bot. 66, 647-656. https://doi. org/10.1093/jxb/eru336.
- Zheng, X., Tan, D.X., Allan, A.C., Zuo, B., Zhao, Y., Reiter, R.J., Wang, L., Wang, Z., Guo, Y., Zhou, J., 2017. Chloroplastic biosynthesis of melatonin and its involvement in protection of plants from salt stress. Sci. Rep. 7, 41236. https://doi.org/10.1038/ srep41236.