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从盐生植物獐茅中克隆和鉴定高亲和钾转运体(AlHKT2;1)基因启动子。

Molecular cloning and characterization of high-affinity potassium transporter (AlHKT2;1) gene promoter from halophyte Aeluropus lagopoides.

机构信息

Division of Plant Omics, CSIR-Central Salt and Marine Chemicals Research Institute (CSIR-CSMCRI), Council of Scientific and Industrial Research (CSIR), Gijubhai Badheka Marg, Bhavnagar 364 002, Gujarat, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.

Division of Plant Omics, CSIR-Central Salt and Marine Chemicals Research Institute (CSIR-CSMCRI), Council of Scientific and Industrial Research (CSIR), Gijubhai Badheka Marg, Bhavnagar 364 002, Gujarat, India.

出版信息

Int J Biol Macromol. 2021 Jun 30;181:1254-1264. doi: 10.1016/j.ijbiomac.2021.05.038. Epub 2021 May 12.

Abstract

HKT subfamily II functions as Na- K co-transporter and prevents plants from salinity stress. A 760 bp promoter region of AlHKT2;1 was isolated, sequenced and cloned. The full length promoter D1, has many cis-regulatory elements like MYB, MBS, W box, ABRE etc. involved in abiotic stress responses. D1 and subsequent 5' deletions were cloned into pCAMBIA1301 and studied for its efficacy in stress conditions in heterologous system. Blue colour staining was observed in flower petals, anther lobe, and dehiscence slit of anther in T plants. The T seedlings showed staining in leaf veins, shoot vasculature and root except root tip. T seedlings were subjected to NaCl, KCl, NaCl + KCl and ABA stresses. GUS activity was quantified by 4-methylumbelliferyl glucuronide (4-MUG) assay under control and stress conditions. The smallest deletion- D4 also showed GUS expression but highest activity was observed in D2 as compared to full length promoter and other deletions. The electrophoretic mobility shift assay using stress-induced protein with different promoter deletions revealed more prominent binding in D2. These results suggest that AlHKT2;1 promoter is involved in abiotic stress response and deletion D2 might be sufficient to drive the stress-inducible expression of various genes involved in providing stress tolerance in plants.

摘要

HKT 亚家族 II 作为 Na-K 协同转运蛋白,可防止植物受到盐胁迫。我们分离、测序并克隆了 AlHKT2;1 的 760bp 启动子区域。全长启动子 D1 包含许多参与非生物胁迫响应的顺式调控元件,如 MYB、MBS、W 盒、ABRE 等。D1 及其后续 5' 缺失被克隆到 pCAMBIA1301 中,并在异源系统中研究其在胁迫条件下的功效。T 植株的花瓣、花药裂片和花药开裂处观察到蓝色染色。T 幼苗在叶片叶脉、茎脉和根(除根尖外)中显示染色。T 幼苗受到 NaCl、KCl、NaCl+KCl 和 ABA 胁迫。在对照和胁迫条件下,通过 4-甲基伞形酮葡萄糖醛酸苷(4-MUG)测定法对 GUS 活性进行定量。最小缺失体 D4 也显示 GUS 表达,但与全长启动子和其他缺失体相比,D2 的活性最高。使用不同启动子缺失体的胁迫诱导蛋白进行电泳迁移率变动分析显示,D2 中结合更明显。这些结果表明,AlHKT2;1 启动子参与非生物胁迫响应,缺失 D2 可能足以驱动与提供植物胁迫耐受性相关的各种基因的胁迫诱导表达。

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