首页|党参蛋白激酶SnRK2家族鉴定及其与转录因子的相关性研究

党参蛋白激酶SnRK2家族鉴定及其与转录因子的相关性研究

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目的 通过对党参蛋白激酶SnRK2家族鉴定,以及对其与转录因子的相关性进行初步解析,为党参抗根腐病机制的解析及高抗性优质党参新品种培育提供数据支撑。方法 基于党参转录组,采用生物信息学手段对CpSnRK2基因家族进行系统性研究。结果 在党参中鉴定到6个CpSnRK2基因家族成员(CpSnRK2。1-CpSnRK2。6),属于3个亚家族,同一亚族成员之间的蛋白基序分布相似。表达模式分析表明CpSnRK2 以及转录因子(WRKY、MYB、ERF、bHLH)在尖孢镰刀菌侵染下存在着时间差异性。同时,CpSnRK2基因和转录因子WRKY、MYB、ERF及bHLH之间存在着显著相关性。结论 本研究揭示了CpSnRK2(CpSnRK2。4和CpSnRK2。6)与转录因子WRKY、MYB、ERF以及bHLH共同调控党参对尖孢镰刀菌的响应,为进一步研究CpSnRK2基因对党参根腐病的响应提供了重要线索。
Identification of Protein Kinases SnRK2 Family in Codonopsis pilosula and its Correlation with Transcription Factors
Objective Through the identification of C.pilosula protein kinase SnRK2 family genes and the preliminary analysis of its correlation with transcription factors,this study provides data support for the analysis of the mechanism of C.pilosula root rot resistance and the breeding of new varieties with high resistance and quality.Methods Based on C.pilosula RNA-seq,using bioinformatics method to systematically study the CpSnRK2 gene family.Results Six CpSnRK2(CpSnRK2.1-CpSnRK2.6)genes were identified and these were devided into three subfamilies.And the motif among the same subfamily members was similar.The expression pattern analysis indicated that the expression levels of CpSnRK2 and transcription factors(WRKY,MYB,ERF and bHLH)had temporal differences were in response to Fusarium oxysporum.At the same time,CpSnRK2 genes were significantly correlated with transcription factors WRKY,MYB,ERF and bHLH.Conclusion This study revealed that CpSnRK2(CpSnRK2.4,CpSnRK2.6)and transcription factors WRKY,MYB,ERF and bHLH jointly regulate the response to Fusarium oxysporum,providing important clues for further research on the response of CpSnRK2 to root rot of C.pilosula.

C.pilosulaRoot rotSnRK2TranscriptomeExpression analysisTranscription factors

程宇飞、董林林、郭笑彤

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鲁东大学农学院 烟台 264025

中国中医科学院中药研究所 北京 100700

党参 根腐病 SnRK2 转录组 表达模式 转录因子

国家科技部国家重点研发计划国家科技部国家重点研发计划

2022YFC35018042018YFC1706302

2024

世界科学技术-中医药现代化
中科院科技政策与管理科学研究所,中国高技术产业发展促进会

世界科学技术-中医药现代化

CSTPCD北大核心
影响因子:1.175
ISSN:1674-3849
年,卷(期):2024.26(2)
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