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作物学报 ›› 2026, Vol. 52 ›› Issue (3): 722-734.doi: 10.3724/SP.J.1006.2026.54105

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

甘蔗CLC基因家族鉴定与表达分析

杨宗桃1,2(), 杨婷1,2, 王禹童1,2, 艾静1,2, 李燕烨1,2, 刘家勇1,2, 邓军1,2, 赵勇1,2,*(), 张跃彬1,2   

  1. 1热带作物生物育种全国重点实验室, 云南昆明 650000
    2云南省农业科学院甘蔗研究所, 云南开远 661699
  • 收稿日期:2025-09-01 接受日期:2025-11-18 出版日期:2026-03-12 网络出版日期:2025-12-03
  • 通讯作者: *赵勇, E-mail: 18087395132@163.com
  • 作者简介:E-mail: fafuyangzongtao@163.com
  • 基金资助:
    云南省科技厅科技计划农业联合专项(202301BD070001-213);财政部和农业农村部国家现代农业产业技术体系建设专项(CARS-17);云南种子种业联合实验室项目(202205AR070001-13);云南省农业科学院科研预研项目(2024KYZX-02);“兴滇英才支持计划”云岭学者专项(XDYC-YLXZ-2022-0038)

Identification and expression analysis of the CLC gene family in sugarcane

Yang Zong-Tao1,2(), Yang Ting1,2, Wang Yu-Tong1,2, Ai Jing1,2, Li Yan-Ye1,2, Liu Jia-Yong1,2, Deng Jun1,2, Zhao Yong1,2,*(), Zhang Yue-Bin1,2   

  1. 1National Key Laboratory for Biological Breeding of Tropical Crops, Kunming 650000, Yunnan, China
    2Sugarcane Research Institute, Yunnan Academy of Agricultural Sciences, Kaiyuan 661699, Yunnan, China
  • Received:2025-09-01 Accepted:2025-11-18 Published:2026-03-12 Published online:2025-12-03
  • Contact: *赵勇, E-mail: 18087395132@163.com
  • Supported by:
    Yunnan Provincial Department of Science and Technology Science and Technology Plan Agricultural Joint Special Project(202301BD070001-213);China Agriculture Research System of MOF and MARA(CARS-17);Yunnan Seed Industry Joint Laboratory Project(202205AR070001-13);Pre-research Project of Yunnan Academy of Agricultural Sciences(2024KYZX-02);Project of Supporting Talents in Xingdian-Yunling Scholars Special Project(XDYC-YLXZ-2022-0038)

摘要:

氯离子通道(chloride channel, CLC)基因家族在植物液泡硝酸盐储存过程中发挥关键作用, 但其在复杂基因组作物甘蔗中尚未被系统鉴定。本研究基于割手密(Saccharum spontaneum)基因组数据, 鉴定出29个SsCLC基因, 分布于21条染色体上, 可分为6个亚族(Group a、Group c、Group d、Group e、Group f和Group g)。基因结构和motif分析表明该家族成员较为保守。共线性分析显示, SsCLC基因家族主要通过全基因组/片段复制事件扩增, 并受到纯化选择。启动子顺式作用元件分析表明, SsCLC富含激素响应(50.00%)、生长发育(42.86%)及胁迫响应(7.14%)等相关元件。以割手密82-1及其3个杂交后代为材料, 农艺性状调查显示杂交后代在茎径、叶长、锤度、鲜重和干重上均显著优于亲本; 转录组与qRT-PCR分析发现, 75.86%的SsCLC基因(22/29)在杂交种根中表达上调。本研究首次系统鉴定了SsCLC基因家族, 揭示了其在杂交种根中普遍上调的表达模式与优良农艺性状密切相关, 为解析甘蔗“高贵化”过程中的氮素高效利用机制提供了重要基因资源。

关键词: 甘蔗, CLC基因家族, 转录组学, 表达分析, 氮素

Abstract:

The chloride channel (CLC) gene family plays a crucial role in nitrate storage within plant vacuoles. However, its characteristics remain largely unexplored in the complex genome of sugarcane. In this study, we systematically identified 29 CLC genes (SsCLCs) from the Saccharum spontaneum genome. These SsCLCs were distributed across 21 chromosomes and phylogenetically classified into six subgroups (Groups a, c, d, e, f, and g). The gene family exhibited conserved structures and motif compositions. Genomic collinearity analysis indicated that the expansion of SsCLC was mainly driven by whole-genome or segmental duplication events under strong purifying selection. Promoter analysis revealed a high abundance of cis-acting elements associated with hormone responses (50.00%), growth and development (42.86%), and stress responses (7.14%). Furthermore, in a comparison between S. spontaneum Yunnan 82-1 and its three hybrid progenies, the hybrids exhibited significant improvements in key agronomic traits, including stalk diameter, leaf length, brix, fresh weight, and dry weight. Consistently, transcriptome and qRT-PCR analyses showed that 75.86% (22 out of 29) of the SsCLC genes were upregulated in the roots of the hybrids. This study presents the first comprehensive genomic characterization of the SsCLC gene family and highlights its potential role in improving nitrogen use efficiency during sugarcane nobilization through root-specific gene upregulation, thereby offering valuable genetic resources for breeding nitrogen-efficient sugarcane cultivars.

Key words: sugarcane, CLC gene family, transcriptomics, expression analysis, nitrogen

附表1

实时荧光定量PCR引物"

基因名称
Gene name
正向引物
Forward primer (5′-3′)
反向引物
Reverse primer (5′-3′)
SsCLC-a1 AGCTTATGCACTGGGAGCTG ATGACGAGGTGATGTTGCCT
SsCLC-a2 CAACTCCGGCAACTTCAAGC AAGATGAGCAGCGAGTCGAG
SsCLC-a3 TCTTGGCTCTTGCGTCTCAT GCCAGTCGTGCTTGAACAGA
SsCLC-c1 AATGTCACTGGCAAAAGCGG ATTCTCAGTGCGTCTGGTGT
SsCLC-c2 TTGCGGTGGTATTGAAGGGG ACATGATCAATCCACCTTTCCCA
SsCLC-c3 CCATGAACACCACCTCCCAG TGCTGTGAAGTACTCGTAGTCG
SsCLC-c4 CCTCGACTACGAGTACTTCAC GCAGCAGCAGGTGCTATGTA
SsCLC-c5 CGACTACGAGTACTTCACAGC AGGTGCTATGTAAGCGCAGA
SsCLC-c6 GCCTCGACTACGAGTACTTCAC AGGTGCTATGTAAGCGCAGA
SsCLC-c7 GGTCGGTGAAGTGGGAGAAGG ATGCATACTCGTAATCGAGGCT
SsCLC-c8 GCGGGACGATGCGGATGAC TTGGCGATGAGCAGCACGAG
SsCLC-d1 CCATCGAGAGCCTCGACTAC CCAGCTCGTTCAATTTGCCA
SsCLC-d2 GCGGACGGCGAGTTCTTAT GACGTAGTAGGGCACCCAGA
SsCLC-d3 CTAAATGGCGGCGAACGCAT CAGTAGTGGCAGCACAAAGG
SsCLC-d4 CTAAATGGCGGCGAACGCAT CATGGGCTGCATTTCCTCAG
SsCLC-e1 AGAAAAGATGGCTCCCTCCG GAGGGCTCCGATCGCTCA
SsCLC-e2 GAGAAAAGACGGCTCCCTCC CCGTGAATCGTGATTTGGGC
SsCLC-f1 TCACCTCCATTTACGACTGC AGAACAGTTACCAGCAGCAGA
SsCLC-f2 TTCGTCGTTCCTCGGTTCTG GTTCGGTGCTGGTCTACTCG
SsCLC-f3 GGATACTGCTGATCCCGGTG GTTGATTCGTTGCCTCTGCC
SsCLC-f4 AAACGTGGTGCTGGCCGTAG CCACCGCTCAAGCTCTTCCC
SsCLC-f5 CTCGTCGGCTGCCTCCTTG TGCCTGCCCATGCCCATTC
SsCLC-f6 CGTCGGCTGCCTCCTTGG TGCCTGCCCATGCCCATTC
SsCLC-f7 GCCAGTCACCTCGCCATCG TCCGCCAGTCGTGCTTGAAC
SsCLC-g1 GCGGTGCCACAAGGAGTACG GGCGATGGTGTCCTGCTTCC
SsCLC-g2 ACCTGCTGGTGCTGCTCAAG AGTCCTCCGCCTGGAACCTC
SsCLC-g3 TCTCCTCCGGCTCGTCCTTC TGGTGTTGGAGTGCGTGTGG
SsCLC-g4 GGCCACATCCTGCGCTACG CCGAGGTTGGCGACGAAGC
SsCLC-g5 TCTCCTCCGGCTCGTCCTTC TGGTGTTGGAGTGCGTGTGG
25s-RNA1 ATAACCGCATCAGGTCTCCAAG CCTCAGAGCCAATCCTTTTCC

图1

水稻、小麦、拟南芥、大豆与SsCLC蛋白的系统进化分析 不同分组的颜色标识如下: 分组a (青色), 分组b (黑色), 分组c (红色), 分组d (蓝色), 分组e (紫色), 分组f (绿色), 分组g (棕色)。"

附表2

SsCLC蛋白基本信息"

基因名称
Gene name
基因 ID
Gene ID
染色体定位
Chr.
localization
氨基酸数目
Amino acid (aa)
相对分子量Molecular weight (kD) 等电点pI 不稳定系数
Instability index
脂肪指数
Aliphatic index
疏水性
Grand average of hydropathicity
亚细胞定位预测
Subcellular localization
SsCLC-a1 Sspon.08G0019260-3D Chr. 8D 801 87.85 6.38 45.48 106.99 0.282 质膜
Plasma membrane
SsCLC-a2 Sspon.08G0019260-2C Chr. 8C 754 82.90 9.16 40.23 115.86 0.475 质膜
Plasma membrane
SsCLC-a3 Sspon.08G0019260-1B Chr. 8B 778 85.07 9.16 39.23 109.58 0.368 质膜
Plasma membrane
SsCLC-c1 Sspon.04G0009220-1A Chr. 4A 716 76.98 6.83 34.86 100.54 0.335 质膜
Plasma membrane
SsCLC-c2 Sspon.04G0009220-3C Chr. 4C 750 80.76 6.98 36.64 99.11 0.288 质膜
Plasma membrane
SsCLC-c3 Sspon.04G0009220-2B Chr. 5B 723 78.29 5.91 38.76 104.83 0.360 质膜
Plasma membrane
SsCLC-c4 Sspon.04G0009220-4D Chr. 5D 730 78.53 6.20 38.99 102.90 0.360 质膜
Plasma membrane
SsCLC-c5 Sspon.04G0009220-1P Chr. 5A 689 74.38 6.65 42.03 99.70 0.276 质膜
Plasma membrane
SsCLC-c6 Sspon.04G0009220-2P Chr. 5C 600 64.57 6.09 40.55 95.98 0.241 质膜
Plasma membrane
SsCLC-c7 Sspon.03G0029010-1B Chr. 3B 1240 132.22 8.36 32.67 106.15 0.461 质膜
Plasma membrane
SsCLC-c8 Sspon.03G0029010-3D Chr. 3D 730 77.95 8.49 34.21 105.79 0.448 质膜
Plasma membrane
SsCLC-d1 Sspon.01G0025410-2B Chr. 1B 829 91.61 8.78 39.12 99.79 0.111 质膜
Plasma membrane
SsCLC-d2 Sspon.01G0025410-3C Chr. 1C 740 81.33 7.89 37.67 102.09 0.253 质膜
Plasma membrane
SsCLC-d3 Sspon.01G0025410-1A Chr. 1A 796 87.41 8.39 37.50 103.09 0.256 质膜
Plasma membrane
SsCLC-d4 Sspon.01G0025410-1P Chr. 1A 410 44.29 7.09 30.49 97.78 0.340 质膜
Plasma membrane
SsCLC-e1 Sspon.03G0004960-1A Chr. 3A 725 77.67 6.32 52.27 98.10 0.186 质膜
Plasma membrane
SsCLC-e2 Sspon.03G0004960-2B Chr. 3B 779 83.88 6.60 51.03 94.67 0.089 叶绿体, 质膜
Chloroplast, plasma membrane
SsCLC-f1 Sspon.04G0004760-4D Chr. 4D 352 36.98 7.65 48.36 89.38 0.017 线粒体, 叶绿体, 质膜
Mitochondrial, chloroplast, plasma membrane
SsCLC-f2 Sspon.04G0004760-1A Chr. 4A 803 85.43 7.57 42.60 96.14 0.049 质膜
Plasma membrane
SsCLC-f3 Sspon.04G0004760-2B Chr. 4B 771 82.09 6.98 40.19 98.37 0.129 质膜
Plasma membrane
SsCLC-f4 Sspon.06G0000980-3C Chr. 6C 630 67.82 6.35 42.54 100.48 0.181 质膜
Plasma membrane
SsCLC-f5 Sspon.06G0000980-2B Chr. 6B 752 79.97 6.07 43.51 97.71 0.116 质膜
Plasma membrane
SsCLC-f6 Sspon.06G0000980-1A Chr. 6A 720 76.41 6.06 44.55 94.89 0.063 叶绿体, 质膜
Chloroplast, plasma membrane
SsCLC-f7 Sspon.06G0000980-4D Chr. 6D 676 71.74 5.97 44.08 93.28 −0.008 线粒体, 叶绿体, 质膜
Mitochondrial, chloroplast, plasma membrane
SsCLC-g1 Sspon.04G0016160-2B Chr. 4B 796 86.56 8.89 44.05 106.04 0.340 质膜
Plasma membrane
SsCLC-g3 Sspon.05G0022270-2C Chr. 5C 815 88.48 8.51 39.87 103.36 0.314 质膜
Plasma membrane
SsCLC-g4 Sspon.05G0022270-1B Chr. 5B 815 88.50 8.58 39.86 103.13 0.313 质膜
Plasma membrane
SsCLC-g5 Sspon.05G0022270-3D Chr. 5D 814 88.42 8.58 39.66 103.13 0.306 质膜
Plasma membrane

图2

SsCLC基因的染色体定位 不同分组的颜色标识如下: 分组a (青色), 分组c (红色), 分组d (蓝色), 分组e (紫色), 分组f (绿色), 分组g (棕色)。"

图3

SsCLC基因的保守基序与基因结构 左侧为SsCLC基因家族成员进化树, 各分组由不同颜色的线条表示, 分别为分组a (青色), 分组c (红色), 分组d (蓝色), 分组e (紫色), 分组f (绿色), 分组g (棕色); CDS: 编码序列; UTR: 非编码区。"

图4

SsCLC基因启动子顺式作用元件分析 左侧为SsCLC基因家族成员进化树, 各分组由不同颜色的线条表示, 分别为分组a (青色), 分组c (红色), 分组d (蓝色), 分组e (紫色), 分组f (绿色), 分组g (棕色)。"

图5

SsCLC基因的复制类型、Ka/Ks及共线性分析 图A中, n表示各复制类型的基因数目, 百分比为其在SsCLC基因家族中的占比。图C中的红色线条指示共线性基因对, 而不同颜色的字体则代表不同的进化分组: 分组a (青色), 分组c (红色), 分组d (蓝色), 分组e (紫色), 分组f (绿色), 分组g (棕色)。"

图6

甘蔗与水稻、玉米、高粱CLC基因的共线性分析 图中染色体命名如下: Ss1A、Os1、Zm1和Sb1分别指代割手密1A染色体、水稻1号染色体、玉米1号染色体和高粱1号染色体。其他染色体缩写均依此规则生成。"

图7

割手密种云南82-1及其杂交种农艺性状比较 YN82-1表示割手密种云南82-1。N1、N2、N3分别指以YN82-1为亲本, 通过多代杂交培育出的3个独立后代品系。误差线为每组处理的标准误差(n = 3)。柱上不同小写字母表示在P < 0.05水平显著性差异。"

图8

基于转录组的SsCLC基因在根中的表达热图 左侧为SsCLC基因家族成员进化树, 不同颜色代表不同分组, 青色、红色、蓝色、紫色、绿色和棕色线条分别代表分组a、分组c、分组d、分组e、分组f和分组g; FPKM表示0、0.20、0.40、0.60、0.80、1.00, 由蓝变红, 数值越大, 颜色越红, 表明表达量越高。"

图9

qRT-PCR验证SsCLC基因在根中的相对表达量 缩写同图7。误差线为每组处理的标准误差(n = 3)。柱上不同小写字母表示在P < 0.05水平显著性差异。"

[1] Yang Y Y, Gao S W, Jiang Y, et al. The physiological and agronomic responses to nitrogen dosage in different sugarcane varieties. Front Plant Sci, 2019, 10: 406.
doi: 10.3389/fpls.2019.00406 pmid: 31024584
[2] Liu Y L, Duan X L, Zhao X D, et al. Diverse nitrogen signals activate convergent ROP2-TOR signaling in Arabidopsis Dev Cell, 2021, 56: 1283-1295.
doi: 10.1016/j.devcel.2021.03.022
[3] Hui Q L, Song T, Yang D T, et al. Identification and characterization of key genes for nitrogen utilization from Saccharum spontaneum sub-genome in modern sugarcane cultivar. Int J Mol Sci, 2025, 26: 226.
doi: 10.3390/ijms26010226
[4] Wang Y Y, Cheng Y H, Chen K E, et al. Nitrate transport, signaling, and use efficiency. Annu Rev Plant Biol, 2018, 69: 85-122.
doi: 10.1146/arplant.2018.69.issue-1
[5] Bell M J, Garside A, Halpin N V, et al. Interactions between rotation breaks, tillage and N management on sugarcane grown at Bundaberg and Ingham. In: Bruce R C, eds. 32nd Conference of the Australian Society of Sugar Cane Technologists. Bundaberg, Qld., Australia Australian Society of Sugar Cane Technologists, 2010. pp 119-139.
[6] Park E, Campbell E B, MacKinnon R. Structure of a CLC chloride ion channel by cryo-electron microscopy. Nature, 2017, 541: 500-505.
doi: 10.1038/nature20812
[7] Sun H J, Shen L L, Qin Y X, et al. CLC-Nt1 affects Potato Virus Y infection via regulation of endoplasmic reticulum luminal Ph. New Phytol, 2018, 220: 539-552.
doi: 10.1111/nph.2018.220.issue-2
[8] Wei Q J, Liu Y Z, Zhou G F, et al. Overexpression of CsCLC, a chloride channel gene from poncirus trifoliata, enhances salt tolerance in Arabidopsis. Plant Mol Biol Rep, 2013, 31: 1548-1557.
doi: 10.1007/s11105-013-0592-1
[9] Wang S, Su S Z, Wu Y, et al. Overexpression of maize chloride channel gene ZmCLC-d in Arabidopsis thaliana improved its stress resistance. Biol Plant, 2015, 59: 55-64.
doi: 10.1007/s10535-014-0468-8
[10] Liu X, Pi B Y, Pu J W, et al. Genome-wide analysis of chloride channel-encoding gene family members and identification of CLC genes that respond to Cl-/salt stress in upland cotton. Mol Biol Rep, 2020, 47: 9361-9371.
doi: 10.1007/s11033-020-06023-z
[11] Xing A Q, Ma Y C, Wu Z C, et al. Genome-wide identification and expression analysis of the CLC superfamily genes in tea plants (Camellia sinensis). Funct Integr Genomics, 2020, 20: 497-508.
doi: 10.1007/s10142-019-00725-9
[12] Lurin C, Geelen D, Barbier-Brygoo H, et al. Cloning and functional expression of a plant voltage-dependent chloride channel. Plant Cell, 1996, 8: 701-711.
doi: 10.1105/tpc.8.4.701 pmid: 8624442
[13] Hechenberger M, Schwappach B, Fischer W N, et al. A family of putative chloride channels from Arabidopsis and functional complementation of a yeast strain with a CLC gene disruption. J Biol Chem, 1996, 271: 33632-33638.
doi: 10.1074/jbc.271.52.33632 pmid: 8969232
[14] Zhou G A, Qiu L J. Identification and functional analysis on abiotic stress response of soybean Cl- channel gene GmCLCnt. Agric Sci China, 2010, 9: 199-206.
doi: 10.1016/S1671-2927(09)60084-5
[15] Mao P J, Run Y H, Wang H H, et al. Genome-wide identification and functional characterization of the chloride channel TaCLC gene family in wheat (Triticum aestivum L.). Front Genet, 2022, 13: 846795.
doi: 10.3389/fgene.2022.846795
[16] Ma J, Li S, Zaman S, et al. CLC gene family in Solanum lycopersicum: genome-wide identification, expression, and evolutionary analysis of tomato in response to salinity and Cd stress. Front Plant Sci, 2025, 16: 1547723.
doi: 10.3389/fpls.2025.1547723
[17] von der Fecht-Bartenbach J, Bogner M, Dynowski M, et al. CLC-b-mediated NO3-/H+ exchange across the tonoplast of Arabidopsis vacuoles. Plant Cell Physiol, 2010, 51: 960-968.
doi: 10.1093/pcp/pcq062 pmid: 20430762
[18] Zifarelli G, Pusch M. CLC transport proteins in plants. FEBS Lett, 2010, 584: 2122-2127.
doi: 10.1016/j.febslet.2009.12.042 pmid: 20036660
[19] Wege S, Jossier M, Filleur S, et al. The proline 160 in the selectivity filter of the Arabidopsis NO3-/H+ exchanger AtCLCa is essential for nitrate accumulation in planta. Plant J, 2010, 63: 861-869.
doi: 10.1111/tpj.2010.63.issue-5
[20] De Angeli A, Monachello D, Ephritikhine G, et al. The nitrate/proton antiporter AtCLCa mediates nitrate accumulation in plant vacuoles. Nature, 2006, 442: 939-942.
doi: 10.1038/nature05013
[21] Hodin J, Lind C, Marmagne A, et al. Proton exchange by the vacuolar nitrate transporter CLCa is required for plant growth and nitrogen use efficiency. Plant Cell, 2023, 35: 318-335.
doi: 10.1093/plcell/koac325
[22] Jossier M, Kroniewicz L, Dalmas F, et al. The Arabidopsis vacuolar anion transporter, AtCLCc, is involved in the regulation of stomatal movements and contributes to salt tolerance. Plant J, 2010, 64: 563-576.
doi: 10.1111/tpj.2010.64.issue-4
[23] Guo W, Zuo Z L, Cheng X, et al. The chloride channel family gene CLCd negatively regulates pathogen-associated molecular pattern (PAMP)-triggered immunity in Arabidopsis. J Exp Bot, 2014, 65: 1205-1215.
doi: 10.1093/jxb/ert484
[24] Marmagne A, Vinauger-Douard M, Monachello D, et al. Two members of the Arabidopsis CLC (chloride channel) family, AtCLCe and AtCLCf, are associated with thylakoid and Golgi membranes, respectively. J Exp Bot, 2007, 58: 3385-3393.
pmid: 17872921
[25] Nguyen C T, Agorio A, Jossier M, et al. Characterization of the chloride channel-like, AtCLCg, involved in chloride tolerance in Arabidopsis thaliana. Plant Cell Physiol, 2016, 57: 764-775.
doi: 10.1093/pcp/pcv169 pmid: 26556649
[26] 曾廷儒, 张静, 张登峰, 等. 玉米ZmCLCa基因克隆及其对氮素吸收的功能验证. 植物遗传资源学报, 2017, 18: 112-116.
Zeng T R, Zhang J, Zhang D F, et al. Cloning of ZmCLCa gene in maize and its functional characterization of nitrogen absorption. J Plant Genet Resour, 2017, 18: 112-116 (in Chinese with English abstract).
[27] Nakamura A, Fukuda A, Sakai S, et al. Molecular cloning, functional expression and subcellular localization of two putative vacuolar voltage-gated chloride channels in rice (Oryza sativa L.). Plant Cell Physiol, 2006, 47: 32-42.
doi: 10.1093/pcp/pci220 pmid: 16249326
[28] Song J F, Han M Y, Zhu X Y, et al. MhCLC-c1, a Cl channel c homolog from Malus hupehensis, alleviates NaCl-induced cell death by inhibiting intracellular Cl-accumulation. BMC Plant Biol, 2023, 23: 306.
doi: 10.1186/s12870-023-04270-3
[29] Wei Q J, Gu Q Q, Wang N N, et al. Molecular cloning and characterization of the chloride channel gene family in trifoliate orange. Biol Plant, 2015, 59: 645-653.
doi: 10.1007/s10535-015-0532-z
[30] Wei P P, Wang L C, Liu A L, et al. GmCLC1 confers enhanced salt tolerance through regulating chloride accumulation in soybean. Front Plant Sci, 2016, 7: 1082.
doi: 10.3389/fpls.2016.01082 pmid: 27504114
[31] 周慧文, 陆桂军, 吴建明, 等. 中国甘蔗种业发展研究进展. 广西科学, 2023, 30(3): 421-433.
Zhou H W, Lu G J, Wu J M, et al. Research progress of sugarcane seed industry in China. Guangxi Sci, 2023, 30(3): 421-433 (in Chinese with English abstract).
[32] Lu G L, Liu P R, Wu Q B, et al. Sugarcane breeding: a fantastic past and promising future driven by technology and methods. Front Plant Sci, 2024, 15: 1375934.
doi: 10.3389/fpls.2024.1375934
[33] Zhan J, Zhou Y F, Yang L S, et al. Low ammonium and high nitrate input improves nitrogen use efficiency and growth in sugarcane through coordinated reprogramming of nitrogen and carbon metabolism. Plant Physiol Biochem, 2025, 229: 110354.
doi: 10.1016/j.plaphy.2025.110354
[34] Zhang J S, Zhang X T, Tang H B, et al. Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. Nat Genet, 2018, 50: 1565-1573.
doi: 10.1038/s41588-018-0237-2
[35] Gasteiger E, Gattiker A, Hoogland C, et al. ExPASy: the proteomics server for in-depth protein knowledge and analysis. Nucleic Acids Res, 2003, 31: 3784-3788.
doi: 10.1093/nar/gkg563 pmid: 12824418
[36] Chou K C, Shen H B. Cell-PLoc: a package of web servers for predicting subcellular localization of proteins in various organisms. Nat Protoc, 2008, 3: 153-162.
doi: 10.1038/nprot.2007.494
[37] Bailey T L, Boden M, Buske F A, et al. MEME SUITE: tools for motif discovery and searching. Nucleic Acids Res, 2009, 37: W202-W208.
doi: 10.1093/nar/gkp335
[38] Hu B, Jin J P, Guo A Y, et al. GSDS 2.0: an upgraded gene feature visualization server. Bioinformatics, 2015, 31: 1296-1297.
doi: 10.1093/bioinformatics/btu817 pmid: 25504850
[39] Chen C J, Chen H, Zhang Y, et al. TBtools: an integrative toolkit developed for interactive analyses of big biological data. Mol Plant, 2020, 13: 1194-1202.
doi: S1674-2052(20)30187-8 pmid: 32585190
[40] Lescot M, Déhais P, Thijs G, et al. PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Res, 2002, 30: 325-327.
[41] Wang Y P, Tang H B, Debarry J D, et al. MCScanX: a toolkit for detection and evolutionary analysis of gene synteny and collinearity. Nucleic Acids Res, 2012, 40: e49.
[42] 阙友雄, 许莉萍, 徐景升, 等. 甘蔗基因表达定量PCR分析中内参基因的选择. 热带作物学报, 2009, 30: 274-278.
Que Y X, Xu L P, Xu J S, et al. Selection of control genes in real-time qPCR analysis of gene expression in sugarcane. Chin J Trop Crops, 2009, 30: 274-278 (in Chinese with English abstract).
[43] Livak K J, Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods, 2001, 25: 402-408.
doi: 10.1006/meth.2001.1262 pmid: 11846609
[44] Wang P P, Moore B M, Panchy N L, et al. Factors influencing gene family size variation among related species in a plant family, Solanaceae. Genome Biol Evol, 2018, 10: 2596-2613.
doi: 10.1093/gbe/evy193 pmid: 30239695
[45] Wang J, Li Y X, Zhu F, et al. Genome-wide analysis of nitrate transporter (NRT/NPF) family in sugarcane Saccharum spontaneum L. Trop Plant Biol, 2019, 12: 133-149.
doi: 10.1007/s12042-019-09220-8
[46] 李旭娟, 李纯佳, 田春艳, 等. 甘蔗硝酸盐转运蛋白1/肽转运蛋白家族6.4基因(ScNPF6.4)克隆及其调控分蘖功能分析. 作物学报, 2024, 50: 2131-2142.
doi: 10.3724/SP.J.1006.2024.44002
Li X J, Li C J, Tian C Y, et al. Identification of nitrate transporter protein 1/peptide transporter protein family 6.4 gene (ScNPF6.4) and functional analysis of its regulation of tillering in sugarcane. Acta Agron Sin, 2024, 50: 2131-2142 (in Chinese with English abstract).
doi: 10.3724/SP.J.1006.2024.44002
[47] Wu Z L, Gao X N, Zhang N N, et al. Genome-wide identification and transcriptional analysis of ammonium transporters in Saccharum. Genomics, 2021, 113: 1671-1680.
doi: 10.1016/j.ygeno.2021.04.001 pmid: 33838277
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