| [1] | De Castro O, Gargiulo R, Del Guacchio E, et al. A molecular survey concerning the origin of Cyperus esculentus (Cyperaceae, Poales): two sides of the same coin (weed vs. crop) [J]. Annals of Botany, 2015, 115(5): 733−745. https://doi.org/10.1093/aob/mcv001 doi: 10.1093/aob/mcv001 |
| [2] | 肖艳华, 邹智, 赵永国, 等. 油莎豆乙酰乳酸合酶基因CeALS的克隆与分析[J]. 生物技术通报, 2022, 38(4): 184−192. https://doi.org/10.13560/j.cnki.biotech.bull.1985.2021-1198 doi: 10.13560/j.cnki.biotech.bull.1985.2021-1198 |
| [3] | 邹智, 赵永国, 张丽, 等. 基于单分子实时测序的油莎豆全长转录组分析[J]. 中国油料作物学报, 2021, 43(2): 229−235. https://doi.org/10.19802/j.issn.1007-9084.2020230 doi: 10.19802/j.issn.1007-9084.2020230 |
| [4] | 邹智, 肖艳华, 张丽, 等. 油莎豆5-烯醇式丙酮酰莽草酸-3-磷酸合酶基因CeEPSPS的克隆与分析[J]. 热带作物学报, 2023, 44(1): 26−34. https://doi.org/10.3969/j.issn.1000-2561.2023.01.004 doi: 10.3969/j.issn.1000-2561.2023.01.004 |
| [5] | Pascual B, Maroto J V, López-Galarza S, et al. Chufa (Cyperus esculentus L. var. sativus boeck. ): an unconventional crop. studies related to applications and cultivation [J]. Economic Botany, 2000, 54(4): 439−448. https://doi.org/10.1007/BF02866543 doi: 10.1007/BF02866543 |
| [6] | 张学昆. 我国油莎豆产业研发进展报告[J]. 中国农村科技, 2019(4): 67−69. https://doi.org/10.3969/j.issn.1005-9768.2019.04.022 doi: 10.3969/j.issn.1005-9768.2019.04.022 |
| [7] | Knazicka Z, Jurikova T, Kovacikova E, et al. Biological properties, mineral composition, and health-promoting potential of tiger nut tubers (Cyperus esculentus L. ) as a novel and underutilized food source [J]. Foods, 2026, 15(2): 191. https://doi.org/10.3390/FOODS15020191 doi: 10.3390/FOODS15020191 |
| [8] | Bates P D, Stymne S, Ohlrogge J. Biochemical pathways in seed oil synthesis [J]. Current Opinion in Plant Biology, 2013, 16(3): 358−364. https://doi.org/10.1016/j.pbi.2013.02.015 doi: 10.1016/j.pbi.2013.02.015 |
| [9] | 张鸿杰, 王阳昕, 于佩田, 等. 植物油脂生物合成多层级转录调控网络研究进展[J]. 中国油料作物学报, 2025, 47(6): 1317−1334. https://doi.org/10.19802/j.issn.1007-9084.2025006 doi: 10.19802/j.issn.1007-9084.2025006 |
| [10] | Focks N, Benning C. wrinkled1: a novel, low-seed-oil mutant of Arabidopsis with a deficiency in the seed-specific regulation of carbohydrate metabolism [J]. Plant Physiology, 1998, 118(1): 91−101. https://doi.org/10.1104/pp.118.1.91 doi: 10.1104/pp.118.1.91 |
| [11] | Behera J R, Rahman M M, Bhatia S, et al. Functional and predictive structural characterization of WRINKLED2, a unique oil biosynthesis regulator in avocado [J]. Frontiers in Plant Science, 2021, 12: 648494. https://doi.org/10.3389/fpls.2021.648494 doi: 10.3389/fpls.2021.648494 |
| [12] | Kilaru A, Cao X, Dabbs P B, et al. Oil biosynthesis in a basal angiosperm: transcriptome analysis of Persea Americana mesocarp [J]. BMC Plant Biology, 2015, 15: 203. https://doi.org/10.1186/s12870-015-0586-2 doi: 10.1186/s12870-015-0586-2 |
| [13] | 徐硕. 油莎豆块茎表达WRI类基因的克隆与鉴定[D]. 海口: 海南大学, 2022. https://doi.org/10.27073/d.cnki.ghadu.2022.001219 |
| [14] | Fields S, Song O K. A novel genetic system to detect protein-protein interactions [J]. Nature, 1989, 340(6230): 245−246. https://doi.org/10.1038/340245a0 doi: 10.1038/340245a0 |
| [15] | 肖艳华. 油莎豆内参照基因的挖掘及除草剂靶标基因ALS和EPSPS的克隆与功能初探[D]. 武汉: 中南民族大学, 2023. https://doi.org/10.27710/d.cnki.gznmc.2023.000885 |
| [16] | Sharif R, Raza A, Chen P, et al. HD-ZIP gene family: potential roles in improving plant growth and regulating stress-responsive mechanisms in plants [J]. Genes, 2021, 12(8): 1256. https://doi.org/10.3390/genes12081256 doi: 10.3390/genes12081256 |
| [17] | Gong S H, Ding Y F, Hu S S, et al. The role of HD-Zip class I transcription factors in plant response to abiotic stresses [J]. Physiologia Plantarum, 2019, 167(4): 516−525. https://doi.org/10.1111/ppl.12965 doi: 10.1111/ppl.12965 |
| [18] | Kumar S, Choudhary P, Gupta M, et al. VASCULAR PLANT ONE-ZINC FINGER1 (VOZ1) and VOZ2 interact with CONSTANS and promote photoperiodic flowering transition [J]. Plant Physiology, 2018, 176(4): 2917−2930. https://doi.org/10.1104/pp.17.01562 doi: 10.1104/pp.17.01562 |
| [19] | Nakai Y, Fujiwara S, Kubo Y, et al. Overexpression of VOZ2 confers biotic stress tolerance but decreases abiotic stress resistance in Arabidopsis [J]. Plant Signaling & Behavior, 2013, 8(3): e23358. https://doi.org/10.4161/psb.23358 doi: 10.4161/psb.23358 |
| [20] | Nakai Y, Nakahira Y, Sumida H, et al. Vascular plant one-zinc-finger protein 1/2 transcription factors regulate abiotic and biotic stress responses in Arabidopsis [J]. The Plant Journal, 2013, 73(5): 761−775. https://doi.org/10.1111/tpj.12069 doi: 10.1111/tpj.12069 |
| [21] | Sun T J, Nitta Y, Zhang Q, et al. Antagonistic interactions between two MAP kinase cascades in plant development and immune signaling [J]. The EMBO Reports, 2018, 19(7): e45324. https://doi.org/10.15252/embr.201745324 doi: 10.15252/embr.201745324 |
| [22] | Wang Y, Liu K, Liao H, et al. The plant WNK gene family and regulation of flowering time in Arabidopsis [J]. Plant Biology, 2008, 10(5): 548−562. https://doi.org/10.1111/j.1438-8677.2008.00072.x doi: 10.1111/j.1438-8677.2008.00072.x |
| [23] | Zhang B G, Liu K D, Zheng Y, et al. Disruption of AtWNK8 enhances tolerance of Arabidopsis to salt and osmotic stresses via modulating proline content and activities of catalase and peroxidase [J]. International Journal of Molecular Sciences, 2013, 14(4): 7032−7047. https://doi.org/10.3390/ijms14047032 doi: 10.3390/ijms14047032 |
| [24] | Zirngibl M E, Araguirang G E, Kitashova A, et al. Triose phosphate export from chloroplasts and cellular sugar content regulate anthocyanin biosynthesis during high light acclimation [J]. Plant Communications, 2023, 4(1): 100423. https://doi.org/10.1016/j.xplc.2022.100423 doi: 10.1016/j.xplc.2022.100423 |
| [25] | Gross L E, Spies N, Simm S, et al. Toc75-V/OEP80 is processed during translocation into chloroplasts, and the membrane-embedded form exposes its POTRA domain to the intermembrane space [J]. FEBS Open Bio, 2020, 10(3): 444−454. https://doi.org/10.1002/2211-5463.12791 doi: 10.1002/2211-5463.12791 |
| [26] | Zhang Y, Feng S H, Chen F F, et al. Arabidopsis DDB1-CUL4 ASSOCIATED FACTOR1 forms a nuclear E3 ubiquitin ligase with DDB1 and CUL4 that is involved in multiple plant developmental processes [J]. The Plant Cell, 2008, 20(6): 1437−1455. https://doi.org/10.1105/tpc.108.058891 doi: 10.1105/tpc.108.058891 |
| [27] | Ul Haq S, Khan A, Ali M, et al. Heat shock proteins: dynamic biomolecules to counter plant biotic and abiotic stresses [J]. International Journal of Molecular Sciences, 2019, 20(21): 5321. https://doi.org/10.3390/ijms20215321 doi: 10.3390/ijms20215321 |
| [28] | García-García C, Frieda K L, Feoktistova K, et al. Factor-dependent processivity in human eIF4A DEAD-box helicase [J]. Science, 2015, 348(6242): 1486−1488. https://doi.org/10.1126/science.aaa5089 doi: 10.1126/science.aaa5089 |
| [29] | Chen K M, Holmström M, Raksajit W, et al. Small chloroplast-targeted DnaJ proteins are involved in optimization of photosynthetic reactions in Arabidopsis thaliana [J]. BMC Plant Biology, 2010, 10: 43. https://doi.org/10.1186/1471-2229-10-43 doi: 10.1186/1471-2229-10-43 |
| [30] | Hershko A, Ciechanover A, Heller H, et al. Proposed role of ATP in protein breakdown: conjugation of protein with multiple chains of the polypeptide of ATP-dependent proteolysis [J]. Proceedings of the National Academy of Sciences of the United States of America, 1980, 77(4): 1783−1786. https://doi.org/10.1073/pnas.77.4.1783 doi: 10.1073/pnas.77.4.1783 |
| [31] | Stevens L A, Kato J, Kasamatsu A, et al. The ARH and macrodomain families of α-ADP-ribose-acceptor hydrolases catalyze α-NAD+ hydrolysis [J]. ACS Chemical Biology, 2019, 14(12): 2576−2584. https://doi.org/10.1021/acschembio.9b00429 doi: 10.1021/acschembio.9b00429 |
| [32] | Eremina M, Rozhon W, Yang S Q, et al. ENO2 activity is required for the development and reproductive success of plants, and is feedback-repressed by AtMBP-1 [J]. The Plant Journal, 2015, 81(6): 895−906. https://doi.org/10.1111/tpj.12775 doi: 10.1111/tpj.12775 |
| [33] | Chen C, Zhang Y H, Ye P, et al. ENO2 knock-out mutants in Arabidopsis modify the regulation of the gene expression response to NaCl stress [J]. Molecular Biology Reports, 2018, 45(5): 1331−1338. https://doi.org/10.1007/s11033-018-4292-7 doi: 10.1007/s11033-018-4292-7 |
| [34] | Yan C X, Yan Z Y, Wang Y Z, et al. Tudor-SN, a component of stress granules, regulates growth under salt stress by modulating GA20ox3 mRNA levels in Arabidopsis [J]. Journal of Experimental Botany, 2014, 65(20): 5933−5944. https://doi.org/10.1093/jxb/eru334 doi: 10.1093/jxb/eru334 |
| [35] | Carpenter J L, Ploense S E, Snustad D P, et al. Preferential expression of an alpha-tubulin gene of Arabidopsis in pollen [J]. The Plant Cell, 1992, 4(5): 557−571. https://doi.org/10.1105/tpc.4.5.557 doi: 10.1105/tpc.4.5.557 |
| [36] | Ni L, Wang Q W, Chen C, et al. OsDMI3-mediated OsUXS3 phosphorylation improves oxidative stress tolerance by modulating OsCATB protein abundance in rice [J]. Journal of Integrative Plant Biology, 2022, 64(5): 1087−1101. https://doi.org/10.1111/jipb.13255 doi: 10.1111/jipb.13255 |
| [37] | Ju J, Aoyama T, Yashiro Y, et al. Structure of the Caenorhabditis elegans m6A methyltransferase METT10 that regulates SAM homeostasis [J]. Nucleic Acids Research, 2023, 51(5): 2434−2446. https://doi.org/10.1093/nar/gkad081 doi: 10.1093/nar/gkad081 |
| [38] | To A, Joubès J, Barthole G, et al. WRINKLED transcription factors orchestrate tissue-specific regulation of fatty acid biosynthesis in Arabidopsis [J]. The Plant Cell, 2012, 24(12): 5007−5023. https://doi.org/10.1105/tpc.112.106120 doi: 10.1105/tpc.112.106120 |
| [39] | Mitsuda N, Hisabori T, Takeyasu K, et al. VOZ;Isolation and characterization of novel vascular plant transcription factors with a one-zinc finger from Arabidopsis thaliana [J]. Plant and Cell Physiology, 2004, 45(7): 845−854. https://doi.org/10.1093/pcp/pch101 doi: 10.1093/pcp/pch101 |
| [40] | Celesnik H, Ali G S, Robison F M, et al. Arabidopsis thaliana VOZ (Vascular plant One-Zinc finger) transcription factors are required for proper regulation of flowering time [J]. Biology Open, 2013, 2(4): 424−431. https://doi.org/10.1242/bio.20133764 doi: 10.1242/bio.20133764 |
| [41] | Nakai Y, Fujiwara S, Kubo Y, et al. Overexpression of VOZ2 confers biotic stress tolerance but decreases abiotic stress resistance in Arabidopsis [J]. Plant Signaling & Behavior, 2013, 8(3): e23358. doi:10.4161/psb.23358 (查阅网上资料,本条文献与第19条重复,请确认) |
| [42] | Lee H G, Park M E, Park B Y, et al. The Arabidopsis MYB96 transcription factor mediates ABA-dependent triacylglycerol accumulation in vegetative tissues under drought stress conditions [J]. Plants, 2019, 8(9): 296. https://doi.org/10.3390/plants8090296 doi: 10.3390/plants8090296 |
| [43] | Yang Y, Yu X C, Song L F, et al. ABI4 activates DGAT1 expression in Arabidopsis seedlings during nitrogen deficiency [J]. Plant Physiology, 2011, 156(2): 873−883. https://doi.org/10.1104/pp.111.175950 doi: 10.1104/pp.111.175950 |