In order to study the roles of members of HKT gene fanfily in wheat, TaHKT2 ; 2 was isolated by using homologous cloning strategy and screening genomic BAC library. TaHKT2; 2 genes were mapped on chromosomes 7A, 7B an...In order to study the roles of members of HKT gene fanfily in wheat, TaHKT2 ; 2 was isolated by using homologous cloning strategy and screening genomic BAC library. TaHKT2; 2 genes were mapped on chromosomes 7A, 7B and 7D, named as TaHKT2; 2-7A, TaHKT2; 2-7B, and TaHKT2; 2-7D, respectively. TaHKT2 ; 2 and TaHKT2 ; 1 had the same genetic structure, composed of three exons and two introns, and formed a cluster with TaHKT2 ; 1 on the phylogenetic tree of plant HKT transporters. The coding sequences of TaHKT2 ; 2-7A, TaHKT2 ; 2-7B, and TaHKT2 ; 2-7D were 1 602, 1 602 and 1 596 bp long, respectively, but TaHKT2 ;2-7D cDNA sequence was not isolated by RT-PCR in eight wheat varieties. The natural diversity of TaHKT2 ;2 genes was analyzed by cloning and sequencing from 12 wheat varieties. The results showed that TaHKT2;2-7A was found to be more diverse than TaHKT2; 2-7B and TaHKT2; 2-7D. Only a few bases changed in the alleles of TaHKT2 ; 2 genes in wheat. No amino-acid natural variation lay in the P-loops of deduced protein sequences of all alleles of TaHKT2 ; 2 in 12 wheat varieties. The identity of coding sequences was nmch higher than that of 5＇ flanking regions of TaHKT2 ; 2 genes. TaHKT2 ; 2 nfight be selected over the comse of wheat domestication and belonged to domestication gene.展开更多
基金Supported by National Key Research and Development Program of China(2016YFD0101802)Modern Agricultural Science and Technology Innovation Engineering Project of Hebei Province(2017038997)National Natural Science Foundation of Hebei Province(C2014106075)
文摘In order to study the roles of members of HKT gene fanfily in wheat, TaHKT2 ; 2 was isolated by using homologous cloning strategy and screening genomic BAC library. TaHKT2; 2 genes were mapped on chromosomes 7A, 7B and 7D, named as TaHKT2; 2-7A, TaHKT2; 2-7B, and TaHKT2; 2-7D, respectively. TaHKT2 ; 2 and TaHKT2 ; 1 had the same genetic structure, composed of three exons and two introns, and formed a cluster with TaHKT2 ; 1 on the phylogenetic tree of plant HKT transporters. The coding sequences of TaHKT2 ; 2-7A, TaHKT2 ; 2-7B, and TaHKT2 ; 2-7D were 1 602, 1 602 and 1 596 bp long, respectively, but TaHKT2 ;2-7D cDNA sequence was not isolated by RT-PCR in eight wheat varieties. The natural diversity of TaHKT2 ;2 genes was analyzed by cloning and sequencing from 12 wheat varieties. The results showed that TaHKT2;2-7A was found to be more diverse than TaHKT2; 2-7B and TaHKT2; 2-7D. Only a few bases changed in the alleles of TaHKT2 ; 2 genes in wheat. No amino-acid natural variation lay in the P-loops of deduced protein sequences of all alleles of TaHKT2 ; 2 in 12 wheat varieties. The identity of coding sequences was nmch higher than that of 5＇ flanking regions of TaHKT2 ; 2 genes. TaHKT2 ; 2 nfight be selected over the comse of wheat domestication and belonged to domestication gene.
