Molecular cloning and expression analysis of the MTN gene during adventitious root development in IBA-induced tetraploid black locust

被引:9
作者
Quan, Jine [1 ]
Zhang, Chunxia [1 ]
Zhang, Sheng [1 ]
Meng, Sen [1 ]
Zhao, Zhong [1 ]
Xu, Xuexuan [1 ]
机构
[1] Northwest A&F Univ, State Key Lab Soil Eros & Dryland Farming Loess P, Yangling 712100, Peoples R China
基金
中国国家自然科学基金;
关键词
5 '-Methylthioadenosine nucleosidase; Adventitious root development; IBA; Tetraploid black locust; ADENOSYL-L-METHIONINE; S-ADENOSYLMETHIONINE DECARBOXYLASE; 5'-METHYLTHIOADENOSINE NUCLEOSIDASE; SPERMIDINE SYNTHASE; ETHYLENE SYNTHESIS; POLYAMINES; AUXIN; METABOLISM; CUTTINGS; RADIATA;
D O I
10.1016/j.gene.2014.10.015
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
5'-Methylthioadenosine (MTA) nucleosidase (MTN) plays a key role in the methionine (Met) recycling pathway of plants. Here, we report the isolation of the 1158 bp full-length, cDNA sequence encoding tetraploid black locust (Robinia pseudoacacia L) MTN (TrbMTN), which contains an open reading frame of 810 bp that encodes a 269 amino acid protein. The amino acid sequence of TrbMTN has more than 88% sequence identity to the MTNs from other plants, with a closer phylogenetic relationship to MTNs from legumes than to MTNs from other plants. Subcellular localization analysis revealed that the TrbMTN gene localizes mainly to the cell membrane and cytoplasm of onion epidermal cells. Indole-3-butyric acid (IBA)-treated cuttings showed higher TrbMTN transcript levels than untreated control cuttings during root primordium and adventitious root formation. TrbMTN and key Met cycle genes showed differential expression in shoots, leaves, stems, and roots, with the highest expression observed in stems. IBA-treated cuttings also showed higher TrbMTN activity than control cuttings during root primordium and adventitious root formation. These results indicate that TrbMTN gene might play an important role in the regulation of IBA-induced adventitious root development in tetraploid black locust cuttings. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 150
页数:11
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