首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >The promoter of the Vicia faba L. gene VfEnod12 encoding an early nodulin is active in cortical cells and nodule primordia of transgenic hairy roots of Vicia hirsuta as well as in the prefixing zone II of mature transgenic V-hirsuta root nodules
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The promoter of the Vicia faba L. gene VfEnod12 encoding an early nodulin is active in cortical cells and nodule primordia of transgenic hairy roots of Vicia hirsuta as well as in the prefixing zone II of mature transgenic V-hirsuta root nodules

机译:编码早期结瘤的蚕豆豌豆基因VfEnod12的启动子在野生豌豆转基因毛状根的皮质细胞和结节原基以及成熟的转基因V-hirsuta根瘤的前缀区II中具有活性

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摘要

A full-length cDNA encoding the Vicia faba L. early nodulin VfEnod12 was isolated. The deduced protein sequence specified a 90 amino acid protein with a MW of 10 206 and contained a putative signal peptide sequence followed by PPX3 repeats characteristic of Enod12 proteins. The VfEnod12 gene was found to be expressed specifically in root nodules as early as 3 days post inoculation with Rhizobium leguminosarum bv. viciae. In mature nodules, VfEnod12 transcripts were confined to the prefixing zone II. A 3.3 kb genomic fragment carrying the complete VfEnod12 coding region was isolated. No intervening sequences were identified in the coding region. A promoter fragment carrying the -692/-41 region mediated reporter gene expression in root cortical cells, module primordia and the prefixing zone II of transgenic Vicia hirsuta root nodules. This fragment contained a putative binding site for the transcription factor ENBP1. In contrast to the highly conserved terminal AATAA motif of the ENBP1 binding site of known Enod12 promoters, the VfEnod12 promoter was characterized by an altered terminal AATAT sequence. This alteration did not interfere with VfEnod12 promoter activity in transgenic roots and nodules of V. hirsuta. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved. [References: 46]
机译:分离了编码蚕豆蚕豆早期结节蛋白VfEnod12的全长cDNA。推导的蛋白质序列指定了一个90个氨基酸的蛋白质,分子量为10206,并包含一个推定的信号肽序列,其后是Enod12蛋白的PPX3重复序列。发现VfEnod12基因最早在豆科根瘤菌接种后3天在根瘤中表达。蚕豆在成熟的结节中,VfEnod12转录本仅限于前缀区域II。分离出带有完整VfEnod12编码区的3.3kb基因组片段。在编码区中没有鉴定出中间序列。在根皮层细胞,模块原基和转基因野豌豆根瘤的前缀区II中,携带-692 / -41区域的启动子片段介导了报告基因的表达。该片段含有一个转录因子ENBP1的假定结合位点。与已知的Enod12启动子的ENBP1结合位点的高度保守的末端AATAA基序相反,VfEnod12启动子的特征是末端AATAT序列发生了改变。这种改变不干扰Vs hirsuta的转基因根和结节中的VfEnod12启动子活性。 (C)2000 Elsevier Science Ireland Ltd.保留所有权利。 [参考:46]

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