Genome-wide characterization and expression analysis of HAK K+ transport family in Ipomoea

被引:15
作者
Jin, Rong [1 ]
Jiang, Wei [1 ]
Yan, Mengxiao [2 ]
Zhang, Aijun [1 ]
Liu, Ming [1 ]
Zhao, Peng [1 ]
Chen, Xiaoguang [1 ]
Tang, Zhonghou [1 ]
机构
[1] Chinese Acad Agr Sci, Sweetpotato Res Inst, Jiangsu Key Lab Sweetpotato Biol & Gent Breeding, Minist Agr,Xuzhou Sweetpotato Res Ctr, Xuzhou 221121, Jiangsu, Peoples R China
[2] Shanghai Chenshan Plant Sci Res Ctr, Shanghai Key Lab Plant Funct Genom & Resources, Shanghai, Peoples R China
关键词
Sweet ptotato; HAK; KUP; KT family; IbHAK; Identification; Gene expression; KT/HAK/KUP POTASSIUM TRANSPORTERS; PLANT-GROWTH; SWEET-POTATO; GENE FAMILY; FUNCTIONAL-CHARACTERIZATION; MOLECULAR-MECHANISMS; ARABIDOPSIS ROOT; ABIOTIC STRESS; SALT STRESS; ACQUISITION;
D O I
10.1007/s13205-020-02552-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The potassium transporter high-affinity K+ transporter/K+ uptake permease/K+ transporter (HAK/KUP/KT) family plays a vital role in potassium uptake, and potassium ion (K+)-mediated environmental stress. In the present study, we identified 22 IbHAK/KUP/KT (HAK) genes in sweet potato [Ipomoea batata (L.) Lam] and the same number of HAK genes from sweet potato wild relative Ipomoea trifida. Phylogeny analysis indicated that the HAKs can be divided into five clades. Chromosomal distribution and genome synteny analyses revealed two tandem-duplicated gene pairs IbHAK16/17 and IbHAK17/18 on chromosomes 13 and eight segmental-duplicated gene pairs on chromosomes 1, 3, 5, 8, 10, 12, 14 among the IbHAK gene family. Eleven orthologous HAK gene pairs between I. batata and I. trifida were involved in the duplication of genomic blocks based on comparative genomic analysis. The Ka/Ks ratios of these IbHAK genes ranged from 0.02 to 0.55(< 1), further indicated that purifying selection was the primary force driving the evolution of HAKs in Ipomoea. A heat map based on RNA-seq data showed that 13 HAKs in Xushu32 (a K+-tolerant sweet potato genotype) and 10 HAKs in Ningzi1 (a K+-sensitive sweet potato genotype) in response to K+ deficiency stress. Quantitative real-time PCR (qRT-PCR) analysis revealed IbHAK2, -3, -8, -10, -11, -18, -19, and -21 were induced in both Xushu32 and Ningzi1 under low K+ stress. Compared with other IbHAK genes, IbHAK8 showed more strongly upregulation after exposure to drought and salt stress. Furthermore, co-expression analysis showed that only IbHAK8 of 22 IbHAK genes involved in network interactions with 30 genes related to abiotic and biotic stresses. Taken together, these results are helpful for further functional studies on IbHAK and molecular breeding of sweet potato.
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页数:18
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