生物技术通报 ›› 2026, Vol. 42 ›› Issue (9): 147-156.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0024
• 植物发育生物学专题 • 上一篇
范丽金1,2,3, 宋晓飞2,3, 李晓丽1,2,3, 闫立英1,2,3(
), 谢洋1,2,3(
)
收稿日期:2026-01-08
出版日期:2026-09-26
发布日期:2026-09-16
通讯作者:
闫立英yanliying66@126.com基金资助:
FAN Li-jin1,2,3, SONG Xiao-fei2,3, LI Xiao-li1,2,3, YAN Li-ying1,2,3(
), XIE Yang1,2,3(
)
Received:2026-01-08
Published:2026-09-26
Online:2026-09-16
摘要:
目的 探究生产中外源生长调节剂调控“顶花带刺”这一关键商品性状的分子机制,为进一步通过分子育种改良黄瓜鲜食品质提供理论依据。 方法 基于转录组与代谢组分析,比较不同发育阶段中蘸花与未蘸花处理下黄瓜雌花花冠的基因表达与代谢物变化,筛选出调控黄瓜雌花花冠延迟开放的关键基因与代谢产物,初步解析黄瓜雌花花冠经处理后延迟脱落的分子调控机制。 结果 在nDF_0d vs DF_0d、nDF_2d vs DF_2d和nDF_4d vs DF_4d 3个比较组中,分别鉴定到3 508、3 581和5 752个差异表达基因。这些基因在植物激素信号转导途径(csv04075)、苯丙烷生物合成途径(csv00940)及苯丙氨酸代谢途径(csv00360)中均显著富集,其中生长素相关基因,包括AUX28(Csa07g1708)、IAA14(Csa02g0970)、GH3.1(Csa06g2748)和ARF19(Csa02g0003)等可能在调控黄瓜花冠延迟开放中发挥关键作用。代谢组分析进一步表明,酚酸、阿魏酸衍生物和类黄酮等次生代谢物在相应处理中积累显著,尤其是苯丙素类和黄酮类化合物,与黄瓜花冠持续开放密切相关,这可能与它们在细胞壁弹性、抗氧化活性和激素调控中的作用有关。 结论 蘸花处理诱导的生长素主导响应,通过拮抗乙烯信号延迟黄瓜花冠开放;未蘸花处理则以乙烯为核心的调控路径促进黄瓜花冠脱落。
范丽金, 宋晓飞, 李晓丽, 闫立英, 谢洋. 基于转录组与代谢组解析黄瓜雌花花冠延迟开放的关键调控通路[J]. 生物技术通报, 2026, 42(9): 147-156.
FAN Li-jin, SONG Xiao-fei, LI Xiao-li, YAN Li-ying, XIE Yang. Integrated Transcriptome and Metabolome Analysis Reveals Key Regulatory Pathways Underlying Delayed Female Corolla Opening in Cucumber[J]. Biotechnology Bulletin, 2026, 42(9): 147-156.
化合物ID Compound_ID | 名字 Name | DF_0d | nDF_0d | DF_2d | nDF_2d | DF_4d | nDF_4d |
|---|---|---|---|---|---|---|---|
| Com_985_neg | 4',5,7-三甲氧基黄酮醇 4',5,7-Trimethoxyflavonol | 99 812 | 2 014 827 | 2 586 900 | 3 922 485 | 97 925 | 5 018 405 |
| Com_427_neg | 阿魏酸异丙酯 Isopropyl ferulate | 21 846 690 | 14 777 483 | 17 392 990 | 19 573 931 | 11 530 980 | 16 744 514 |
| Com_554_neg | 异阿魏酸 Isoferulic acid | 1 221 127 | 4 219 810 | 7 698 845 | 1 494 036 | 5 608 662 | 664 965 |
| Com_757_neg | 紫杉叶素 Taxifolin | 5 801 315 | 20 924 851 | 4 556 372 | 11 860 780 | 2 852 499 | 3 048 801 |
| Com_949_neg | 甲基麦冬酮 A Methylophiopogonone A | 10 963 630 | 12 663 286 | 301 010 | 39 368 378 | 568 404 | 17 869 891 |
| Com_4340_neg | 异香草素 Exoticin | 3 430 495 | 9 128 613 | 10 462 639 | 5 841 462 | 9 034 048 | 5 633 944 |
| Com_4335_neg | 山柰酚-7-O-葡萄糖醛酸苷 kaempferol 7-O-glucuronide | 1 015 134 | 468 478 | 6 944 203 | 5 443 416 | 2 904 047 | 6 374 979 |
| Com_4641_neg | 6-甲氧基山柰酚-3-(6''-乙酰葡萄糖苷) 6-Methoxykaempferol 3-(6''-acetylglucoside) | 193 070 843 | 353 025 210 | 134 610 782 | 314486278 | 86 323 233 | 134 778 258 |
| Com_4079_neg | 5,3',5'-三羟基-3,6,7,8,4'-五甲氧基黄酮 5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone | 5 864 270 | 62 703 343 | 56 892 969 | 128 853 000 | 29 644 666 | 363 265 415 |
| Com_3031_neg | 胡麻黄素 Pedalitin | 14 778 991 | 29 971 631 | 9 555 536 | 25 735 469 | 5 751 055 | 11 617 497 |
| Com_1134_neg | 阿魏酸松柏酯 Coniferyl ferulate | 95 023 | 1 262 222 | 11 012 131 | 2 647 689 | 39 000 914 | 4 963 227 |
| Com_2320_neg | 咖啡酸-4-O-硫酸酯 Caffeic acid 4-O-sulfate | 7 765 051 | 3 391 782 | 562 561 | 2 040 834 | 1 733 624 | 3 814 649 |
| Com_4416_neg | 反式咖啡酸-[芹菜糖基-(1→6)-葡萄糖基]酯 trans-Caffeic acid [apiosyl-(1->6)-glucosyl] ester | 13 375 922 | 22 601 763 | 12 451 711 | 9 133 318 | 25 147 790 | 9 179 527 |
| Com_4640_neg | 3,3',5-三羟基-4'-甲氧基-6,7-亚甲二氧基黄酮-3-葡糖醛酸苷 3,3',5-Trihydroxy-4'-methoxy-6,7-methylenedioxyflavone 3-glucuronide | 28 411 607 | 21 071 365 | 57 485 453 | 71 630 275 | 30 797 856 | 61 048 706 |
| Com_4635_neg | 染料木素-8-C-葡萄糖苷-6″-O-丙二酸酯 Genistein 8-C-glucoside 6″-O-malonate | 6 040 661 | 25 638 724 | 9 716 662 | 43 509 690 | 14 019 377 | 20 772 415 |
| Com_3858_neg | 8-C-对羟基苄基山奈酚 9-8-C-p-Hydroxybenzylkaempferol | 5 899 335 | 176 884 | 6 459 625 | 8 099 458 | 880 644 | 17 677 543 |
| Com_3677_neg | 7,8,3',4',5'-五甲氧基异黄酮 7,8,3',4',5'-Pentamethoxyisoflavone | 6 222 719 | 10 991 494 | 265 441 | 1 086 138 | 2 494 967 | 554 146 |
| Com_4707_neg | 5,7-二羟基-8,3',4',5'-四甲氧基黄酮-6-C-葡萄糖苷 5,7-Dihydroxy-8,3',4',5'-tetramethoxyflavone 6-C-glucoside | 956 993 | 14 674 867 | 1 563 193 | 21 773 921 | 10 957 937 | 18 130 177 |
| Com_4474_neg | 表没食子儿茶素-3-O-阿魏酸酯 Epigallocatechin-3-O-ferulate | 288 455 | 2 801 330 | 10 936 700 | 3 029 505 | 44 030 371 | 10 394 177 |
| Com_3950_neg | 5,6,7,3',4',5'-六甲氧基黄酮 5,6,7,3',4',5'-Hexamethoxyflavone | 2 250 713 | 16 100 866 | 28 902 532 | 29 435 394 | 14 485 535 | 26 265 020 |
表1 负离子模式下不同阶段蘸花和未蘸花黄瓜花冠中鉴定出的苯丙素类相关代谢物
Table 1 Phenylpropanoid-related metabolites identified in dipped and non-dipped cucumber corollas at different stages under negative ion mode
化合物ID Compound_ID | 名字 Name | DF_0d | nDF_0d | DF_2d | nDF_2d | DF_4d | nDF_4d |
|---|---|---|---|---|---|---|---|
| Com_985_neg | 4',5,7-三甲氧基黄酮醇 4',5,7-Trimethoxyflavonol | 99 812 | 2 014 827 | 2 586 900 | 3 922 485 | 97 925 | 5 018 405 |
| Com_427_neg | 阿魏酸异丙酯 Isopropyl ferulate | 21 846 690 | 14 777 483 | 17 392 990 | 19 573 931 | 11 530 980 | 16 744 514 |
| Com_554_neg | 异阿魏酸 Isoferulic acid | 1 221 127 | 4 219 810 | 7 698 845 | 1 494 036 | 5 608 662 | 664 965 |
| Com_757_neg | 紫杉叶素 Taxifolin | 5 801 315 | 20 924 851 | 4 556 372 | 11 860 780 | 2 852 499 | 3 048 801 |
| Com_949_neg | 甲基麦冬酮 A Methylophiopogonone A | 10 963 630 | 12 663 286 | 301 010 | 39 368 378 | 568 404 | 17 869 891 |
| Com_4340_neg | 异香草素 Exoticin | 3 430 495 | 9 128 613 | 10 462 639 | 5 841 462 | 9 034 048 | 5 633 944 |
| Com_4335_neg | 山柰酚-7-O-葡萄糖醛酸苷 kaempferol 7-O-glucuronide | 1 015 134 | 468 478 | 6 944 203 | 5 443 416 | 2 904 047 | 6 374 979 |
| Com_4641_neg | 6-甲氧基山柰酚-3-(6''-乙酰葡萄糖苷) 6-Methoxykaempferol 3-(6''-acetylglucoside) | 193 070 843 | 353 025 210 | 134 610 782 | 314486278 | 86 323 233 | 134 778 258 |
| Com_4079_neg | 5,3',5'-三羟基-3,6,7,8,4'-五甲氧基黄酮 5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone | 5 864 270 | 62 703 343 | 56 892 969 | 128 853 000 | 29 644 666 | 363 265 415 |
| Com_3031_neg | 胡麻黄素 Pedalitin | 14 778 991 | 29 971 631 | 9 555 536 | 25 735 469 | 5 751 055 | 11 617 497 |
| Com_1134_neg | 阿魏酸松柏酯 Coniferyl ferulate | 95 023 | 1 262 222 | 11 012 131 | 2 647 689 | 39 000 914 | 4 963 227 |
| Com_2320_neg | 咖啡酸-4-O-硫酸酯 Caffeic acid 4-O-sulfate | 7 765 051 | 3 391 782 | 562 561 | 2 040 834 | 1 733 624 | 3 814 649 |
| Com_4416_neg | 反式咖啡酸-[芹菜糖基-(1→6)-葡萄糖基]酯 trans-Caffeic acid [apiosyl-(1->6)-glucosyl] ester | 13 375 922 | 22 601 763 | 12 451 711 | 9 133 318 | 25 147 790 | 9 179 527 |
| Com_4640_neg | 3,3',5-三羟基-4'-甲氧基-6,7-亚甲二氧基黄酮-3-葡糖醛酸苷 3,3',5-Trihydroxy-4'-methoxy-6,7-methylenedioxyflavone 3-glucuronide | 28 411 607 | 21 071 365 | 57 485 453 | 71 630 275 | 30 797 856 | 61 048 706 |
| Com_4635_neg | 染料木素-8-C-葡萄糖苷-6″-O-丙二酸酯 Genistein 8-C-glucoside 6″-O-malonate | 6 040 661 | 25 638 724 | 9 716 662 | 43 509 690 | 14 019 377 | 20 772 415 |
| Com_3858_neg | 8-C-对羟基苄基山奈酚 9-8-C-p-Hydroxybenzylkaempferol | 5 899 335 | 176 884 | 6 459 625 | 8 099 458 | 880 644 | 17 677 543 |
| Com_3677_neg | 7,8,3',4',5'-五甲氧基异黄酮 7,8,3',4',5'-Pentamethoxyisoflavone | 6 222 719 | 10 991 494 | 265 441 | 1 086 138 | 2 494 967 | 554 146 |
| Com_4707_neg | 5,7-二羟基-8,3',4',5'-四甲氧基黄酮-6-C-葡萄糖苷 5,7-Dihydroxy-8,3',4',5'-tetramethoxyflavone 6-C-glucoside | 956 993 | 14 674 867 | 1 563 193 | 21 773 921 | 10 957 937 | 18 130 177 |
| Com_4474_neg | 表没食子儿茶素-3-O-阿魏酸酯 Epigallocatechin-3-O-ferulate | 288 455 | 2 801 330 | 10 936 700 | 3 029 505 | 44 030 371 | 10 394 177 |
| Com_3950_neg | 5,6,7,3',4',5'-六甲氧基黄酮 5,6,7,3',4',5'-Hexamethoxyflavone | 2 250 713 | 16 100 866 | 28 902 532 | 29 435 394 | 14 485 535 | 26 265 020 |
图1 不同阶段蘸花和未蘸花黄瓜花冠的形态差异nDF_0d、nDF_2d、nDF_4d表示未蘸花处理0、2和4 d,DF_0d、DF_2d、DF_4d表示蘸花处理0、2和4 d;比例尺为1 cm。下同
Fig. 1 Morphological differences between dipped and non-dipped cucumber corollas at different stagesnDF_0d, nDF_2d, and nDF_4d indicates 0, 2, and 4 d without flower dipping treatment, while DF_0d, DF_2d, and DF_4d represent 0, 2, and 4 d with flower dipping treatment. The scale is 1 cm. The same below
图2 不同发育阶段黄瓜蘸花处理与未蘸花处理花冠中差异表达基因的鉴定A:主成分分析;B:韦恩图;C:火山图分析
Fig. 2 Identification of differentially expressed genes between dipped and non-dipped cucumber corollas at different developmental stagesA: The principal component analysis. B: Venn diagram. C: Volcano plot analysis
图3 不同发育阶段蘸花与未蘸花黄瓜花冠差异表达基因的GO富集分析A‒C:分别为nDF_0d与DF_0d、nDF_2d与DF_2d、nDF_4d与DF_4d差异表达基因的GO富集分析图
Fig. 3 GO enrichment analysis of differentially expressed genes between dipped and non-dipped cucumber corollas at different stagesA‒C: Represent the GO enrichment analysis of DEGs nDF_0d vs. DF_0d, nDF_2d vs. DF_2d, and nDF_4d vs. DF_4d
图4 不同发育阶段蘸花与未蘸花黄瓜花冠差异表达基因的KEGG富集分析A‒C:分别为nDF_0d与DF_0d(A)、nDF_2d与DF_2d(B)、nDF_4d与DF_4d(C)差异表达基因的KEGG显著性富集分析图;D:富集于植物激素信号转导(csv04075)、苯丙烷类生物合成(csv00940)和苯丙氨酸代谢(csv00360)的差异表达基因热图
Fig. 4 KEGG enrichment analysis of differentially expressed genes between dipped and non-dipped cucumber corollas at different stagesA‒C: KEGG significance enrichment analysis of DEGs nDF_0d vs. DF_0d (A), nDF_2d vs. DF_2d (B), and nDF_4d vs. DF_4d (C), respectively. D: Heatmap of DEGs enriched in plant hormone signal transduction (csv04075), phenylpropanoid biosynthesis (csv00940), and phenylalanine metabolism (csv00360)
图5 黄瓜雌花花冠开放延迟相关DEGs表达水平的验证*P<0.05, **P<0.01, ns: no significant difference (P>0.05)
Fig. 5 Verification of the expressions of DEGs related to the delayed opening of female flower corollas in cucumber
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