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绣球'杜丽'AP3基因克隆与基因编辑载体构建

李童 王月莹 赵惠恩

广西植物2024,Vol.44Issue(2):257-266,10.
广西植物2024,Vol.44Issue(2):257-266,10.DOI:10.11931/guihaia.gxzw202204002

绣球'杜丽'AP3基因克隆与基因编辑载体构建

AP3 gene cloning and gene-editing vector construction of Hydrangea macrophylla'Dooley'

李童 1王月莹 1赵惠恩1

作者信息

  • 1. 花卉种质创新与分子育种北京市重点实验室,林木花卉遗传育种教育部重点实验室,国家花卉工程技术研究中心,城乡生态环境北京实验室,北京林业大学 园林学院,北京 100083
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摘要

Abstract

Hydrangea macrophylla is a garden plant widely cultivated in Asia,America,and Europe with its inflorescence as main ornamental feature.It is commonly used in interior decoration and landscape creation.To investigate the role of AP3 gene in hydrangea during calyx formation,H.macrophylla'Dooley'was used as the material.The MADS-box Class B gene HmAP3 was cloned,and its gene function was predicted by bioinformatics analysis.To explore methods for quicker breeding new varieties,highly-specific editing targets were screened and CRISPR/Cas9 gene-editing vectors were constructed.The vector sequence was integrated into the H.macrophylla genome by agrobacterium-mediated transformation.The results were as follows:(1)The cDNA sequence full length of HmAP3 was 546 bp,encoding 181 amino acids.Its amino acid sequence was 100%similar to the reference sequence and 58.8%similar to Arabidopsis thaliana.(2)AP3 differed greatly in different genera.Within the same genus,the main structure of AP3 protein was conserved and differed only in a few motifs.(3)There were two highly specific targets in HmAP3.Sequencing results indicated that two single-target CRISPR/Cas9 gene-editing vectors were constructed successfully.(4)There were five resistant buds with Cas9 sequences in their genomes.However,their target sequences did not change due to the absence of Cas9 expression.In this study,the potential of AP3 gene in the breeding work of double flower phenotype was investigated,and a preliminary exploration of CRISPR/Cas9 gene-editing technology for Hydrangea macrophylla was conducted.These results provide a basis for the breeding of H.macrophylla.

关键词

绣球/MADS-box家族/AP3/CRISPR/Cas9/载体构建

Key words

Hydrangea macrophylla/MADS-box family/AP3/CRISPR/Cas9/vector construction

分类

农业科技

引用本文复制引用

李童,王月莹,赵惠恩..绣球'杜丽'AP3基因克隆与基因编辑载体构建[J].广西植物,2024,44(2):257-266,10.

基金项目

国家林业和草原局引进国际先进林业科学技术项目(2015-4-15). (2015-4-15)

广西植物

OA北大核心CSTPCD

1000-3142

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