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http://dx.doi.org/10.5808/GI.2020.18.3.e29

The comparative gene expression concern to the seed pigmentation in maize (Zea mays L.)  

Sa, Kyu Jin (Department of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University)
Choi, Ik-Young (Department of Agriculture and Life Industry, Kangwon National University)
Lee, Ju Kyong (Department of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University)
Abstract
Maize seed pigmentation is one of the important issue to develop maize seed breeding. The differently gene expression was characterized and compared for three inbred lines, such as the pigment accumulated seed (CM22) and non-pigmented seed (CM5 and CM19) at 10 days after pollination. We obtained a total of 63,870, 82,496, and 54,555 contigs by de novo assembly to identify gene expression in the CM22, CM5, and CM19, respectably. In differentially expressed gene analysis, it was revealed that 7,044 genes were differentially expressed by at least two-fold, with 4,067 upregulated in colored maize inbred lines and 2,977 upregulated in colorless maize inbred lines. Of them,18 genes were included to the anthocyanin biosynthesis pathways, while 15 genes were upregulated in both CM22/5 and CM22/19. Additionally, 37 genes were detected in the metabolic pathway concern to the seed pigmentation by BINs analysis using MAPMAN software. Finally, these differently expressed genes may aid in the research on seed pigmentation in maize breeding programs.
Keywords
anthocyanin; colored and colorless maize; gene expression; maize; RNA sequence;
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1 Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 2014;30:2114-2120.   DOI
2 Thimm O, Blasing O, Gibon Y, Nagel A, Meyer S, Kruger P, et al. MAPMAN: a user-driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes. Plant J 2004;37:914-939.   DOI
3 Navarro A, Torres A, Fernandez-Aulis F, Pena C. Bioactive compounds in pigmented maize. In: Corn: Production and Human Health in Changing Climate (Amanullah, Fahad S, eds.). London: IntechOpen, 2018. pp. 69-91.
4 Das PK, Geul B, Choi SB, Yoo SD, Park YI. Photosynthesis-dependent anthocyanin pigmentation in Arabidopsis. Plant Signal Behav 2011;6:23-25.   DOI
5 Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet 2009;10:57-63.   DOI
6 Chen J, Zeng B, Zhang M, Xie S, Wang G, Hauck A, et al. Dynamic transcriptome landscape of maize embryo and endosperm development. Plant Physiol 2014;166:252-264.   DOI
7 Prioul JL, Mechin V, Lessard P, Thevenot C, Grimmer M, Chateau-Joubert S, et al. A joint transcriptomic, proteomic and metabolic analysis of maize endosperm development and starch filling. Plant Biotechnol J 2008;6:855-869.   DOI
8 Fu J, Thiemann A, Schrag TA, Melchinger AE, Scholten S, Frisch M. Dissecting grain yield pathways and their interactions with grain dry matter content by a two-step correlation approach with maize seedling transcriptome. BMC Plant Biol 2010;10:63.   DOI
9 Usadel B, Nagel A, Steinhauser D, Gibon Y, Blasing OE, Redestig H, et al. PageMan: an interactive ontology tool to generate, display, and annotate overview graphs for profiling experiments. BMC Bioinformatics 2006;7:535.   DOI
10 Mol J, Grotewold E, Koes R. How genes paint flowers and seeds. Trends Plant Sci 1998;3:212-217.   DOI
11 Takacs EM, Li J, Du C, Ponnala L, Janick-Buckner D, Yu J, et al. Ontogeny of the maize shoot apical meristem. Plant Cell 2012;24:3219-3234.   DOI
12 Norberto S, Silva S, Meireles M, Faria A, Pintado M, Calhau C. Blueberry anthocyanins in health promotion: a metabolic overview. J Funct Foods 2013;5:1518-1528.   DOI
13 Iordan LH, Martura T, Alionte E, Lazar C. Protein, starch, amino and fatty acids content in corn hybrids developed at NARDI Fundulea in natural climatic conditions. Sci Pap Ser A Agron 2015;58:221-227.
14 Zilic S, Serpen A, Akillioglu G, Gokmen V, Vancetovic J. Phenolic compounds, carotenoids, anthocyanins, and antioxidant capacity of colored maize (Zea mays L.) kernels. J Agric Food Chem 2012;60:1224-1231.   DOI
15 Ford RH. Inheritance of kernel color in corn: explanations and investigations. Am Biol Teach 2000;62:181-188.   DOI
16 Jung TW, Song S, Son BY, Kim JT, Baek SB, Kim CK, et al. A black waxy hybrid corn, "Heukjinjuchal" with good eating quality. Korean J Breed Sci 2009;41:599-602.
17 Petroni K, Pilu R, Tonelli C. Anthocyanins in corn: a wealth of genes for human health. Planta 2014;240:901-911.   DOI
18 Morohashi K, Casas MI, Falcone Ferreyra ML, Falcone Ferreyra L, Mejia-Guerra MK, Pourcel L, et al. A genome-wide regulatory framework identifies maize pericarp color1 controlled genes. Plant Cell 2012;24:2745-2764.   DOI
19 Carey CC, Strahle JT, Selinger DA, Chandler VL. Mutations in the pale aleurone color1 regulatory gene of the Zea mays anthocyanin pathway have distinct phenotypes relative to the functionally similar TRANSPARENT TESTA GLABRA1 gene in Arabidopsis thaliana. Plant Cell 2004;16:450-464.   DOI
20 Park KJ, Park JY, Ryu SH, Seo YH, Choe JK, Yong WS, et al. An anthocyanin-rich grain corn hybrid cultivar, 'Sekso2'. In: Annual Symposium of Korean Society of Breeding Science, 2016 Jun 29-Jul 1, Cheongju, Korea. Suwon: The Korean Society of Breeding Science, 2016. p. 127.
21 Tong W, Kwon SJ, Lee J, Choi IY, Park YJ, Choi SH, et al. Gene set by de novo assembly of Perilla species and expression profiling between P. frutescens (L.) var. frutescens and var. crispa. Gene 2015;559:155-163.   DOI
22 Paschold A, Jia Y, Marcon C, Lund S, Larson NB, Yeh CT, et al. Complementation contributes to transcriptome complexity in maize (Zea mays L.) hybrids relative to their inbred parents. Genome Res 2012;22:2445-2454.   DOI
23 Radchuk V, Borisjuk L. Physical, metabolic and developmental functions of the seed coat. Front Plant Sci 2014;5:510.
24 Kim JS, Lee BH, Kim SH, Ok KH, Cho KY. Responses to environmental and chemical signals for anthocyanin biosynthesis in non-chlorophyllous corn (Zea mays L.) leaf. J Plant Biol 2006;49:16-25.   DOI
25 Li T, Zhang W, Yang H, Dong Q, Ren J, Fan H, et al. Comparative transcriptome analysis reveals differentially expressed genes related to the tissue-specific accumulation of anthocyanins in pericarp and aleurone layer for maize. Sci Rep 2019;9:2485.   DOI
26 Hu QP, Xu JG. Profiles of carotenoids, anthocyanins, phenolics, and antioxidant activity of selected color waxy corn grains during maturation. J Agric Food Chem 2011;59:2026-2033.   DOI
27 Procissi A, Dolfini S, Ronchi A, Tonelli C. Light-dependent spatial and temporal expression of pigment regulatory genes in developing maize seeds. Plant Cell 1997;9:1547-1557.   DOI
28 Park KJ, Ryu SH, Min HK, Seo JS, Park JY, Goh BD, et al. A new black waxy corn hybrid cultivar, 'Miheugchal' with good eating quality and high yield. Korean J Breed Sci 2007;39:106-107.
29 Park KJ, Park JY, Seo YH, Ryu SH, Choi JK, Kim HY. Anthocyanin-rich purple waxy corn single cross hybrid 'Cheongchunchal'. Korean J Breed Sci 2016;48:541-546.   DOI
30 Radicella JP, Brown D, Tolar LA, Chandler VL. Allelic diversity of the maize B regulatory gene: different leader and promoter sequences of two B alleles determine distinct tissue specificities of anthocyanin production. Genes Dev 1992;6:2152-2164.   DOI
31 Kakumanu A, Ambavaram MM, Klumas C, Krishnan A, Batlang U, Myers E, et al. Effects of drought on gene expression in maize reproductive and leaf meristem tissue revealed by RNA-Seq. Plant Physiol 2012;160:846-867.   DOI
32 Lu X, Chen D, Shu D, Zhang Z, Wang W, Klukas C, et al. The differential transcription network between embryo and endosperm in the early developing maize seed. Plant Physiol 2013;162:440-455.   DOI