Ji Huang , Xia Yang , Mei-Mei Wang , Hai-Juan Tang, Ling-Yun Ding, Yin Shen, Hong-Sheng Zhang
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引用次数: 105
Abstract
A cDNA for the gene ZFP182, encoding a C2H2-type zinc finger protein, was cloned from rice by RT-PCR. ZFP182 codes an 18.2 kDa protein with two C2H2-type zinc finger motifs, one nuclear localization signal and one Leu-rich domain. The DLN-box/EAR-motif, which exists in most of plant C2H2-type zinc finger proteins, does not exist in ZFP182. The expression analysis showed that ZFP182 gene was constitutively expressed in leaves, culms, roots and spikes at the adult rice plants, and markedly induced in the seedlings by cold (4 °C), 150 mM NaCl and 0.1 mM ABA treatments. The approximate 1.4 kb promoter region of ZFP182 gene was fused into GUS reporter gene and transformed into tobacco. The histochemical analysis revealed that GUS expression could not be detected in transformed tobacco seedlings under normal conditions, but strongly observed in tobacco leaf discs and the vascular tissue of roots treated with NaCl or KCl. Expression of ZFP182 in transgenic tobacco and overexpression in rice increased plant tolerance to salt stress. These results demonstrated that ZFP182 might be involved in plant responses to salt stress.
利用RT-PCR技术,从水稻中克隆了编码c2h2型锌指蛋白的ZFP182基因cDNA。ZFP182编码一个18.2 kDa的蛋白,包含两个c2h2型锌指基序、一个核定位信号和一个富leu结构域。在大多数植物c2h2型锌指蛋白中存在的DLN-box/ ear基序在ZFP182中不存在。表达分析表明,ZFP182基因在水稻成体叶片、茎、根和穗中均有组成性表达,在低温(4℃)、150 mM NaCl和0.1 mM ABA处理下均有显著诱导。将ZFP182基因约1.4 kb的启动子区域融合到GUS报告基因中,转化到烟草中。组织化学分析表明,在正常条件下,GUS在转化烟草幼苗中未被检测到,但在NaCl或KCl处理的烟草叶盘和根维管组织中有较强的表达。ZFP182在转基因烟草中的表达和在水稻中的过表达提高了植物对盐胁迫的耐受性。这些结果表明ZFP182可能参与了植物对盐胁迫的响应。