Genome-wide Identification, Expression, and Functional Analysis of MdMSI Genes in Apples (Malus domestica Borkh.)

被引:3
|
作者
Wang, Daru [1 ]
Wang, Xun [1 ]
Zhang, Chunling [1 ]
Yang, Kuo [1 ]
Wang, Xinjie [1 ]
Cui, Jianying [1 ]
Liu, Dandan [2 ]
You, Chunxiang [1 ]
机构
[1] Shandong Agr Univ, Coll Hort Sci & Engn, Natl Res Ctr Apple Engn & Technol, Natl Key Lab Crop Biol, Tai An, Shandong, Peoples R China
[2] Yunnan Univ, Coll Agr, Kunming, Yunnan, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
apple; MSI; expression pattern; salt stress; phylogenetic tree; FLOWERING TIME; TRANSCRIPTION FACTOR; DROUGHT TOLERANCE; ARABIDOPSIS MSI1; STRESS-RESPONSE; PROTEIN; CHROMATIN; HOMOLOG; COMPLEX; PLANTS;
D O I
10.3389/fgene.2022.846321
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The multicopy suppressor of IRA (MSI) is a subfamily of WD40 repeat proteins, which is widely involved in plant growth and development. In order to explore the function of MdMSI members in abiotic stress, we identified eight MSI gene family members from the Malus x domestica reference genome. They were distributed on six chromosomes, and they had similar secondary and tertiary structures. We found a variety of regulatory elements in response to hormones and abiotic stress in MdMSI promoters. Through qRT-PCR analysis, it was revealed that MdMSIs were expressed in all tissues, especially in roots. The analysis results also revealed that the expression of MdMSIs was induced in varying degrees under salt, drought stress, and ABA treatments. Furthermore, we obtained the overexpression of MdMSI1-1 transgenic apple calli and Arabidopsis. The overexpression of MdMSI1-1 in calli and Arabidopsis played a negative regulatory role in salt stress response. Our work laid a foundation for further verifying the function of MSI genes under abiotic stress in apples.
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收藏
页数:14
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