鸟苷酸激酶OsGK1对水稻种子发育至关重要

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  • 1南京农业大学 作物遗传与种质创新国家重点实验室/农业部长江中下游粳稻生物学与遗传育种重点实验室/长江流域杂交水稻协同创新中心/江苏省现代作物生产中心,南京 210095
    2连云港市农业科学院 江苏 连云港 222000
*通讯联系人,E-mail: yihuawang@njau.edu.cn

收稿日期: 2018-01-15

  修回日期: 2018-03-17

  网络出版日期: 2018-09-10

基金资助

国家重点研发项目七大农作物育种专项(2016YFD0100101-08);江苏省科技支撑计划资助项目(BE2015363,BE2017368);江苏省农业科技自主创新资金资助项目[CX(16)1029]

The Guanylate Kinase OsGK1 is Essential for Seed Development in Rice

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  • 1State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University/Key Laboratory of Biology, Genetics and Breeding of japonica Rice in Mid-lower Yangtze River, Ministry of Agriculture/The Yangtze River Valley Hybrid Rice Collaboration Innovation Center/Jiangsu Collaboration Innovation Center for Modern Crop Production, Nanjing 210095, China
    2Lianyungang Academy of Agricultural Science, Lianyungang 222000, China
*Corresponding author, E-mail: yihuawang@njau.edu.cn

Received date: 2018-01-15

  Revised date: 2018-03-17

  Online published: 2018-09-10

摘要

【目的】对水稻粉质皱缩突变体fse2进行表型分析及基因克隆,为阐明水稻淀粉合成机制以及胚的发育奠定基础。【方法】fse2来自粳稻品种滇粳优1号的MNU(N-甲基-N-亚硝基脲)诱变突变体库。本研究考查了突变体fse2籽粒的理化性状,利用扫描电镜和半薄切片观察了淀粉颗粒的结构;构建了fse2与N22的F2群体,通过图位克隆及转基因互补验证确定目标基因;通过qRT-PCR以及GUS活性染色对FSE2进行组织表达分析;免疫印迹分析了突变体中淀粉合成相关基因以及线粒体基因的蛋白变化。【结果】fse2籽粒粉质皱缩,千粒重显著下降;胚乳中淀粉颗粒变小变圆,排列松散,不能形成正常的复合淀粉颗粒;突变体中总淀粉、直链淀粉含量均显著下降,脂肪含量显著上升,突变体淀粉的糊化特性发生明显改变。FSE2编码一个线粒体和质体双定位的鸟苷酸激酶(guanylate kinase),命名为OsGK1。OsGK1在各器官中组成型表达,并在花后6 d的胚乳中表达水平最高。突变体胚乳中淀粉合成相关蛋白水平显著降低,尤其是AGPS2b和PHOI。此外,突变体fse2的胚发育严重受损,导致种子纯合致死;线粒体定位的AOX积累显著增强,而野生型中几乎检测不到,表明线粒体呼吸途径受损。【结论】由于OsGK1的功能缺陷,导致水稻种子中线粒体和造粉体发育异常,进而产生了胚致死以及胚乳粉质皱缩的表型,因此OsGK1对水稻种子的发育至关重要。

本文引用格式

李景芳, 田云录, 刘喜, 刘世家, 陈亮明, 江玲, 张文伟, 徐大勇, 王益华, 万建民 . 鸟苷酸激酶OsGK1对水稻种子发育至关重要[J]. 中国水稻科学, 2018 , 32(5) : 415 -426 . DOI: 10.16819/j.1001-7216.2018.8003

Abstract

【Objective】In this study, the phenotype of the floury and shrunken endosperm mutant fse2 was analyzed. Isolation of the responsible gene will lay a foundation for elucidating the mechanism underlying starch synthesis and embryo development in rice. 【Method】fse2 was obtained from the mutant library of japonica cultivar Dianjingyou 1 induced with N-Nitroso-N-methylurea. In this study, the physiochemical properties of fse2 endosperm were investigated and the structure of starch grains was observed. An F2 population derived from fse2 and N22 was constructed, then the underlying gene was determined by map-based cloning and complementation tests. qRT-PCR and GUS staining were used to analyze the expression of FSE2. Western blotting was performed to analyze the protein levels of starch synthesis related genes and mitochondrial genes in the mutant. 【Result】Compared with the transparent endosperm of wild type, fse2 displayed a floury and shrunken endosperm, significantly declined 1000-grain weight, smaller and loosely packed irregular compound starch grains. Total starch and amylose content decreased significantly, while the lipid content increased obviously in fse2, and the gelatinization characteristics of fse2 were changed notably. FSE2 encodes a guanylate kinase named OsGK1, which is dual-targeted to both mitochondria and plastids. OsGK1 was constitutively expressed in various organs with the highest level in developing endosperm at 6th day after flowering. The protein levels of most of the starch synthesis related genes in the mutant endosperm were significantly decreased, especially AGPS2b and PHOI. In addition, the homozygous seeds of fse2 were lethal and the development of fse2 embryos was severely arrested. The accumulation of mitochondria AOX was notably elevated, while almost undetectable in the wild type, indicating the mitochondrial respiratory chain was impaired. 【Conclusion】Due to the functional defects of OsGK1, the development of mitochondria and amyloplasts are abnormal, leading to the embryo lethality and a floury and shrunken endosperm.

参考文献

[1] Khush G S.What it will take to feed 5.0 billion rice consumers in 2030.Plant Mol Biol, 2005, 59(1): 1-6.
[2] Zhou Z, Robards K, Heliwell S, Blanchard C.Composition and functional properties of rice.Int J Food Sci Technol, 2002, 37(8): 849-868.
[3] Demirkesen I, Sumnu G, Sahin S.Image analysis of gluten-free breads prepared with chestnut and rice flour and baked in different ovens.Food Bioprocess Technol, 2013, 6(7): 1749-1758.
[4] Patindol J, Wang Y J.Fine structures and physicochemical properties of starches from chalky and translucent rice kernels.J Agric Food Chem, 2003, 51(9): 2777-2784.
[5] Martin C, Smith A M.Starch biosynthesis.Plant Cell, 1995, 7(7): 971-985.
[6] Nakamura Y.Towards a better understanding of the metabolic system for amylopectin biosynthesis in plants: Rice endosperm as a model tissue.Plant & Cell Physiol, 2002, 43(7): 718-725.
[7] Hirose T, Terao T.A comprehensive expression analysis of the starch synthase gene family in rice (Oryza sativa L.). Planta, 2004, 220(1): 9-16.
[8] Ball S G, Morell M K.From bacterial glycogen to starch: Understanding the biogenesis of the plant starch granule.Annu Rev Plant Biol, 2003, 54(1): 207-233.
[9] Colleoni C, Dauvillée D, Mouille G, Morell M, Samuel M, Slomiany M C, Lienard L, Wattebled F, d’Hulst C, Ball S. Biochemical characterization of the Chlamydomonas reinhardtii α-1,4 glucanotransferase supports a direct function in amylopectin biosynthesis. Plant Physiol, 1999, 120(4): 1005-1014.
[10] Dauvillée D, Chochois V, Steup M, Haebel S, Eckermann N, Ritte G, Ral J P, Colleoni C, Hicks G, Wattebled F O, Deschamps P, d’Hulst C O, Liénard L, Cournac L O, Putaux J L O, Dupeyre D, Ball S G O. Plastidial phosphorylase is required for normal starch synthesis in Chlamydomonas reinhardtii. Plant J, 2006, 48(2): 274-285.
[11] Dong X, Zhang D, Liu J, Liu Q Q, Liu H, Tian L, Jiang L, Qu le Q. Plastidial disproportionating enzyme participates in starch synthesis in rice endosperm by transferring maltooligosyl groups from amylose and amylopectin to amylopectin.Plant Physiol, 2015, 169(4): 2496-2512.
[12] Schupp N, Ziegler P.The relation of starch phosphorylases to starch metabolism in wheat.Plant & Cell Physiol, 2004, 45(10): 1471-1484.
[13] Satoh H, Shibahara K, Tokunaga T, Nishi A, Tasaki M, Hwang S K, Okita T W, Kaneko N, Fujita N, Yoshida M, Hosaka Y, Sato A, Utsumi Y, Ohdan T, Nakamura Y.Mutation of the plastidial a-glucan phosphorylase gene in rice affects the synthesis and structure of starch in the endosperm.Plant Cell, 2008, 20(7): 1833-1849.
[14] Pfeilmeier S, Saur I M, Rathjen J P, Zipfel C, Malone J G.High levels of cyclic-di-GMP in plant-associated Pseudomonas correlate with evasion of plant immunity.Mol Plant Pathol, 2016, 17(4): 521-531.
[15] Zrenner R, Stitt M, Sonnewald U, Boldt R.Pyrimidine and purine biosynthesis and degradation in plants.Annu Rev Plant Biol, 2006, 57: 805-836.
[16] Green R, Noller H F.Ribosomes and translation.Annu Rev Biochem, 1997, 66: 679-716.
[17] Sumita K, Lo Y H, Takeuchi K, Senda M, Kofuj S, Ikeda Y, Terakawa J, Sasaki M, Yoshino H, Majd N, Zheng Y X, Kahoud E R, Yokota T, Emerling B M, Asara J M, Ishida T, Locasale J W, Daikoku T, Anastasiou D, Senda T, Sasaki A T.The lipid kinase PI5P4Kβ is an intracellular GTP sensor for metabolism and tumorigenesis.Mol Cell, 2016, 61(2): 187-198.
[18] Caro L G, Palade G E.Protein synthesis, storage, and discharge in the pancreatic exocrine cell. An autoradiographic study. J Cell Biol, 1946, 20(3): 473-495.
[19] Havel P J.Control of energy homeostasis and insulin action by adipocyte hormones: Leptin, acylation stimulating protein, and adiponectin.Curr Opin Lipidol, 2002, 13(1): 51-59.
[20] Stasolla C, Katahira R, Thorpe T A, Ashihara H.Purine and pyrimidine nucleotide metabolism in higher plants.J Plant Physiol, 2003, 160(11): 1271-1295.
[21] Gaidarov I O, Suslov O N, Abdulaev N G.Enzymes of the cyclic GMP metabolism in Bovine retina: I. Cloning and expression of the gene for guanylate kinase. FEBS Lett, 1993, 335(1): 81-84.
[22] Brady W A, Kokoris M S, Fitzgibbon M, Black M E.Cloning, characterization, and modeling of mouse and human guanylate kinases.J Biol Chem, 1996, 271(28): 16734-16740.
[23] Stolworthy T S, Krabbenhoft E, Black M E.A novel Escherichia coli strain allows functional analysis of guanylate kinase drug resistance and sensitivity.Anal Biochem, 2003, 322(1): 40-47.
[24] Beck B J, Huelsmeyer M, Paul S, Downs D M.A mutation in the essential gene gmk(encoding guanylate kinase) generates a requirement for adenine at low temperature in Salmonella enteric. J Bacteriol, 2003, 185(22): 6732-6735.
[25] Gentry D, Bengra C, Ikehara K, Cashel M.Guanylate kinase of Escherichia coli K-12. J Biol Chem, 1993, 268(19): 14316-14321.
[26] Konrad M.Cloning and expression of the essential gene for guanylate kinase from yeast.J Biol Chem, 1992, 267(36): 25652-25655.
[27] Ray B D, Jarori G K, Raghunathan V, Yan H, Rao B D N. Conformations of nucleotides bound to wild type and Y78 F mutant yeast guanylate kinase: Proton two-dimensional transferred NOESY measurements. Biochemistry, 2005, 44(42): 13762 13770.
[28] Kumar V.Cloning and sequence analysis of lily and tobacco guanylate kinases.Mol Biol Rep, 2000, 27(1): 45 49.
[29] Kumar V, Spangenberg O, Konrad M.Cloning of the guanylate kinase homologues AGK-1 and AGK-2 from Arabidopsis thaliana and characterization of AGK-1. Eur J Biochem, 2000, 267(2): 606-615
[30] Sugimoto H, Kusumi K, Tozawa Y, Yazaki H, Kishimoto N, Kikuchi S, Iba K.The virescent-2 mutation inhibits translation of plastid transcripts for the plastid genetic system at an early stage of chloroplast differentiation. Plant & Cell Physiol, 2004, 45(8): 985-996.
[31] Sugimoto H, Kusumi K, Noguchi K, Yano M, Yoshimura A, Iba K.The rice nuclear gene,VIRESCENT 2, is essential for chloroplast development and encodes a novel type of guanylate kinase targeted to plastids and mitochondria. Plant J, 2007, 52(3): 512-527.
[32] Kang H G, Park S, Matsuoka M, An G.White-core endosperm floury endosperm-4 in rice is generated by knockout mutations in the C-type pyruvate orthophosphate dikinase gene (OsPPDKB). Plant J, 2005, 42(6): 901-911.
[33] Peng C, Wang Y, Liu F, Ren Y, Zhou K, Lv J, Zheng M, Zhao M, Zhao S, Zhang L, Wang C, Jiang L, Zhang X, Guo X, Wan J M.FLOURY ENDOSPERM 6 encodes a CBM48 domain-containing protein involved in compound granule formation and starch synthesis in rice endosperm. Plant J, 2014, 77(6): 917-930.
[34] Nishi A, Nakamura Y, Tanaka N, Satoh H.Biochemical and genetic analysis of the effects of Amylose-Extender mutation in rice endosperm. Plant Physiol, 2001, 127(2): 459-472
[35] Ohdan T, Francisco P B Jr, Sawada T, Hirose T, Saltoh H, Nakamura Y. Expression profiling of genes involved in starch synthesis in sink and source organs of rice. J Exp Bot, 2005, 56(422): 3229-3244.
[36] Akihiro T, Mizuno K, Fujimura T.Gene expression of ADP-glucose pyrophosphorylase and starch contents in rice cultured cells are cooperatively regulated by sucrose and ABA.Plant & Cell Physiol, 2005, 46(6): 937-946.
[37] Finnegan P M, Soole K L, Umbach A L.Alternative mitochondrial electron transport proteins in higher plants. //Day D A, Millar A H, Whelan J. Plant Mitochondria: From Genome to Function. The Netherlands: Springer, 2004: 163-230.
[38] Selinshi J, Hartmann A, Kordes A, Deckers-Hebestreit G, Whelan J, Scheibe R.Analysis of post-translational activation of alternative oxidase isoforms.Plant Physiol, 2017, 174(4): 2113-2127.
[39] Zhang Y F, Suzuki M, Sun F, Tan B C.The mitochondrion-targeted PENTATRICOPEPTIDE REPEAT78 protein is required fornad5 mature mRNA stability and seed development in maize. Mol Plant, 2017, 10(10): 1321-1333
[40] Li X J, Zhang Y F, Hou M M, Sun F, Shen Y, Xiu Z H, Wang X, Chen Z L, Sun S S, Small I, Tan B C.Small kernel 1 encodes a pentatricopeptide repeat protein required for mitochondrial nad7 transcript editing and seed development in maize(Zea mays) and rice, 2014, 79(5): 797-809.
[41] Liu Y J, Xiu Z H, Meeley R, Tan B C.Empty Pericarp5 encodes a pentatricopeptide repeat protein that is required for mitochondrial RNA editing and seed development in maize. Plant Cell, 2013, 25(3): 868-883.
[42] Yang Y Z, Ding S, Wang H C, Sun F, Huang W L, Song S, Xu C, Tan B C.The pentatricopeptide repeat protein EMP9 is required for mitochondrial ccmB and rps4 transcript editing, mitochondrial complex biogenesis and seed development in maize. New Phytol, 2017, 214(2): 782-795.
[43] Cai M J, Li S Z, Sun F, Sun Q, Zhao H, Ren X, Zhao Y, Tan B C, Zhang Z, Qiu F.Emp10 encodes a mitochondrial PPR protein that affects the cis-splicing of nad2 intron 1 and seed development in maize. Plant J, 2017, 91(1): 132-144.
[44] Ren X M, Pan Z Y, Zhao H L, Zhao J L, Cai M J, Li J, Zhang Z X, Qiu F Z.EMPTY PERICARP11 serves as a factor for splicing of mitochondrial nad1 intron and is required to ensure proper seed development in maize. J Exp Bot, 2017, 68(16): 4571-4581.
[45] Jiang P F, Wang S L, Jiang H Y, Cheng B J, Wu K Q, Ding Y.The COMPASS-like complex promotes flowering and panicle branching in rice. Plant Physiol, 176(4): 01749.2017. DOI:10.1104/pp.17.01749.
[46] Minkenberg B, Xie K, Yang Y N.Discovery of rice essential genes by characterizing a CRISPR-edited mutation of closely related rice MAP kinase genes.Plant J, 2017, 89(3): 636-648.
[47] Huang X, Peng X, Sun M X.OsGCD1 is essential for rice fertility and required for embryo dorsal-ventral pattern formation and endosperm development.New Phytol, 2017, 215(9): 1039-1058.
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