遗传 ›› 2026, Vol. 48 ›› Issue (6): 614-627.doi: 10.16288/j.yczz.25-349
张曼婷1(
), 卢梓豪1, 聂敏琪1, 谭裕翔1, 梁启梅1, 骆懋彦1, 戴永东1, 李锦涛1, 陈炜1, 陈紫媚1, 和家贤1,2, 李美娜1(
)
收稿日期:2025-12-29
修回日期:2026-03-09
出版日期:2026-06-20
发布日期:2026-04-02
通讯作者:
李美娜,博士,教授,研究方向:大豆杂种优势和生物钟与环境互作。E-mail: limeina@gzhu.edu.cn作者简介:张曼婷,硕士研究生,专业方向:植物学。E-mail: 1436291159@qq.com
基金资助:
Manting Zhang1(
), Zihao Lu1, Minqi Nie1, Yuxiang Tan1, Qimei Liang1, Maoyan Luo1, Yongdong Dai1, Jintao Li1, Wei Chen1, Zimei Chen1, Jiaxian He1,2, Meina Li1(
)
Received:2025-12-29
Revised:2026-03-09
Published:2026-06-20
Online:2026-04-02
Supported by:摘要:
我国的大豆(Glycine max)供给严重依赖国际市场,提升国内自给能力已成为保障粮食安全的紧迫任务。全国土壤普查数据显示,我国拥有约5亿亩盐渍土资源,其中约2亿亩具备农业开发潜力。在耕地资源紧张的背景下,培育耐盐碱大豆新品种,是实现盐碱地资源有效利用、扩大种植面积并应对土壤盐渍化挑战的战略性举措。快速碱化因子(rapid alkalinization factor,RALF)是一类作为配体的植物小肽,通过结合质膜受体复合物启动下游信号,协调植物生长发育与逆境响应。然而RALF小肽在大豆等重要作物中介导盐碱胁迫应答的具体分子机制尚不明确。本研究通过对大豆RALF家族进行表达模式分析,并结合碱性盐处理下的转录组数据,发现拟南芥(Arabidopsis thaliana)的AtRALF34在大豆中的两个同源基因GmRALF34a和GmRALF34b在根中优势表达,且其表达在碱性盐处理后受到显著抑制。利用基因编辑技术获得Gmralf34ab双突变体,该突变体表现为对碱性盐胁迫敏感性增强,相比之下,在中性盐胁迫下,突变体与野生型无显著差异。大田表型鉴定进一步表明,突变体在株高、节数和单株产量等农艺性状上均显著降低。综上,本研究初步揭示了GmRALF34s在大豆响应碱性盐胁迫及盐碱地适应性中扮演着重要角色,为深入解析其分子机制提供了重要遗传材料,并为大豆耐盐碱育种奠定了理论与材料基础。
张曼婷, 卢梓豪, 聂敏琪, 谭裕翔, 梁启梅, 骆懋彦, 戴永东, 李锦涛, 陈炜, 陈紫媚, 和家贤, 李美娜. 大豆快速碱化因子GmRALF34s响应盐碱胁迫的功能研究[J]. 遗传, 2026, 48(6): 614-627.
Manting Zhang, Zihao Lu, Minqi Nie, Yuxiang Tan, Qimei Liang, Maoyan Luo, Yongdong Dai, Jintao Li, Wei Chen, Zimei Chen, Jiaxian He, Meina Li. Functional study of the soybean rapid alkalinization factor GmRALF34s in response to saline-alkali stress[J]. Hereditas(Beijing), 2026, 48(6): 614-627.
表1
本研究所用的引物信息"
| 引物名称 | 引物序列(5′→3′) | 用途 |
|---|---|---|
| sgRNA-1 | CCTGTCCCCTGTCCCCTGTC | 敲除靶点 |
| sgRNA-2 | AGGTTGGCGTGCAGGCGCAG | |
| sgRNA-3 | CCCACGTTGCCGTGCAGGCG | |
| sgRNA-4 | CGTTGCCGTGCAGGCGCACA | |
| TEST | F:TGCTACCCTCATCCATCAGTC | 骨架鉴定 |
| R:TGTTGTGTGGAATTGTGAGCG | ||
| RALF34a | F:ATGGCTTCTTCTCTTCCTCTTC | 靶点测序 |
| R:TCATCTCCGGCAGCGCGTGATG | ||
| RALF34b | F:ATGGCTTCTCTTCTCACCCTCGC | |
| R:TCATCTCCGGCAGCGCGTGATG | ||
| qRT-34a | F:AACTCATACCTGTGACCGTG | qRT-PCR |
| R:TCCGACATGAGGTTCAAGCC | ||
| qRT-34b | F:ATGGCTTCTCTTCTCACCCT | |
| R:ACTTCATCCGCCGCCAGAAC | ||
| F-box | F:ATGGTCGCCGTTTAGAACAC | 内参基因 |
| R:GGGATAACCAGTGCAGAAGC |
图3
大豆GmRALF组织表达特异性及碱性盐胁迫响应 A:大豆RALF家族基因在花、根、VE(emergence)期子叶、叶和种子中的FPKM数值表达热图及系统聚类分析(数据来源Soy OD)。热图颜色梯度代表标准化表达信号值(红色:高表达;蓝色:低表达)。B:公共数据库转录组数据中Glyma.01G186800与Glyma.11G055200在根、子叶、叶、花和种子中的表达丰度。C和D:qRT-PCR验证Glyma.01G186800与Glyma.11G055200在VC(cotyledon)时期根与侧根、子叶、V1(first trifoliolate)时期的茎和叶片的表达丰度。内参基因为F-box。E:RALF家族基因在大豆根组织(50 mmol/L NaHCO3,pH 8.5)碱性盐胁迫处理4 h后的FPKM数值表达热图及系统聚类分析。CK代表对照组(0 mmol/L NaHCO3,pH 5.8),热图颜色梯度代表标准化表达信号值(红色:高表达;蓝色:低表达)。"
图6
大豆GmRALF34s功能缺失突变体在碱性盐胁迫下的表型及生理参数分析 A:碱性盐胁迫下大豆Gmralf34ab双突变体的表型。将5日龄野生型Wm82、Gmralf34ab-1与Gmralf34ab-2双突变体置于0 mmol/L NaHCO3(pH 5.8) (Control)和25 mmol/L NaHCO3(pH 8.3)条件下,生长12天后拍照记录,比例尺为10 cm。B~F:对应处理下野生型Wm82、Gmralf34ab-1与Gmralf34ab-2双突变体的株高、根鲜重、根长、丙二醛(MDA)含量和总叶绿素含量。采用t检验进行显著性分析,ns表示无显著性差异(P>0.05),*P<0.05表示差异显著,**P<0.01和***P<0.001表示差异极显著,n≥6。"
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