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https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
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https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

园艺学报 ›› 2025, Vol. 52 ›› Issue (5): 1301-1316.doi: 10.16420/j.issn.0513-353x.2025-0045

• 遗传育种·种质资源·分子生物学 • 上一篇    下一篇

甘蓝叶酸合成代谢的转录组初步分析

张悦1,2, 冯一了1, 王蓓2, 任文静1, 姜春昱1, 赵新宇1, 王彩红1, 杨丽梅1, 庄木1, 吕红豪1, 王勇1, 张扬勇1,*(), 季家磊1,3,*()   

  1. 1 中国农业科学院蔬菜花卉研究所,蔬菜生物育种全国重点实验室,北京 100081
    2 沈阳农业大学园艺学院,沈阳 110866
    3 中蔬种业科技(重庆)有限公司,重庆 402560
  • 收稿日期:2025-04-13 修回日期:2025-04-27 出版日期:2025-05-23 发布日期:2025-05-21
  • 通讯作者:
  • 基金资助:
    国家重点研发计划项目(2023YFD1200101); 川渝科技创新合作计划项目(CSTB2024TIAD-CYKJCXX0022); 重庆市人民政府与中国农业科学院战略合作资助项目

Preliminary Transcriptome Analysis of Folate Synthesis and Metabolism in Cabbage

ZHANG Yue1,2, FENG Yiliao1, WANG Bei2, REN Wenjing1, JIANG Chunyu1, ZHAO Xinyu1, WANG Caihong1, YANG Limei1, ZHUANG Mu1, LÜ Honghao1, WANG Yong1, ZHANG Yangyong1,*(), JI Jialei1,3,*()   

  1. 1 State Key Laboratory of Vegetable Biobreeding,Institute of Vegetables and Flowers,Chinese Academy of Agricultural Sciences,Beijing 100081,China
    2 College of Horticulture,Shenyang Agricultural University,Shenyang 110161,China
    3 China Vegetable Seed Technology Co., Ltd.(Chongqing),Chongqing 402560,China
  • Received:2025-04-13 Revised:2025-04-27 Published:2025-05-23 Online:2025-05-21

摘要:

对127份甘蓝自交系材料的叶酸组分和含量进行了靶向代谢组分析,确定甘蓝中叶酸主要组分为5-甲基-四氢叶酸(占比60% ~ 80%)和5-甲酰-四氢叶酸(占比15% ~ 25%),筛选出早熟圆球型高叶酸自交系材料Q428和低叶酸自交系材料Q372。通过Q428和Q372比较转录组分析,鉴定出10 305个差异表达基因,在Q428中上调和下调表达的基因分别有5 178、5 127个。GO分析显示,差异表达基因与光合作用、光收集、蛋白质—发色团连接和叶绿素结合等相关;KEGG分析表明,差异表达基因主要集中于碳代谢、氨基酸生物合成及淀粉和蔗糖代谢等通路。通过与24个拟南芥叶酸合成代谢基因的共线性分析,在甘蓝中鉴定到叶酸合成代谢相关基因57个,其中12个关键基因在Q428和Q372中显著差异表达。与Q372相比,Q428中BoGCHI、GDC复合体相关编码基因(BoGCSHBoGCSLBoGCSPBoGCST)、BoMTHFRBoSHMT1a的表达量显著上调,而BoGGH在Q428中表达量显著下调。初步推测上述基因的差异表达是影响甘蓝叶酸含量的关键因素,可作为利用生物育种技术调控甘蓝叶酸含量的分子靶点。

关键词: 甘蓝, 叶酸, 转录组, 代谢组

Abstract:

A targeted metabolomic analysis was conducted on the folate composition and content of 127 cabbage inbred lines. The main folate components in cabbage were identified as 5-methyl- tetrahydrofolate(60%-80% of the total)and 5-formyl-tetrahydrofolate(15%-25% of the total). Early-maturing,round-headed high-folate inbred line Q428 and low-folate inbred line Q372 were selected for further study. Comparative transcriptomic analysis of Q428 and Q372 identified 10 305 differentially expressed genes,with 5 178 genes upregulated and 5 127 genes downregulated in Q428. Gene Ontology analysis indicated that the differentially expressed genes were associated with processes such as photosynthesis,light harvesting,protein-chromophore interactions,and chlorophyll binding. KEGG pathway analysis revealed that these genes were primarily involved in carbon metabolism,amino acid biosynthesis,and starch and sucrose metabolism.Through a collinearity analysis with 24 Arabidopsis folate biosynthesis genes,a total of 57 folate-related genes were identified in cabbage,of which 12 key genes showed significant differential expression between Q428 and Q372. Compared to Q372,the expression levels of BoGCHI,genes associated with the GDC complex(BoGCSHBoGCSLBoGCSPBoGCST),BoMTHFR,and BoSHMT1a were significantly upregulated in Q428,while the expression of BoGGH was significantly downregulated. The differential expression of these genes is preliminarily hypothesized to be a key factor affecting the folate content in cabbage,and these genes could serve as molecular targets for manipulating folate content in cabbage through biotechnological breeding techniques.

Key words: cabbage, folate, transcriptome, metabolome