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编码富含甘氨酸的早期结瘤素的结节特异性VfENOD-GRP3基因位于蚕豆的第一条染色体上,主要在根瘤的II-III区表达。

The nodule-specific VfENOD-GRP3 gene encoding a glycine-rich early nodulin is located on chromosome I of Vicia faba L. and is predominantly expressed in the interzone II-III of root nodules.

作者信息

Küster H, Schröder G, Frühling M, Pich U, Rieping M, Schubert I, Perlick A M, Pühler A

机构信息

Universität Bielefeld, Lehrstuhl für Genetik, Germany.

出版信息

Plant Mol Biol. 1995 Jun;28(3):405-21. doi: 10.1007/BF00020390.

Abstract

A nodule-specific cDNA was isolated from a Vicia faba L. nodule cDNA library. Since time course experiments revealed an early expression of this transcript in the nodule, this cDNA coded for an early nodulin and was designated VfENOD-GRP3. Based on tissue print hybridizations, we found a predominant expression of VfENOD-GRP3 transcripts in the interzone II-III region of broad bean root nodules. The encoded early nodulin ENOD-GRP3 was characterized by an N-terminal signal peptide and a C-terminal domain displaying a glycine content of 31%. Sequence analysis of a genomic VfENOD-GRP3 clone revealed that the signal peptide and the glycine-rich domain were specified by two separate exons. Primer extension experiments identified two adjacent transcription start sites for VfENOD-GRP3 transcripts. The common nodulin sequences 'AAAGAT' and 'CTCTT' were present five and three times on both DNA strands of the putative VfENOD-GRP3 promoter, respectively. Additionally, three sequence motifs resembling organ-specific elements of the soybean lbc3 gene promoter and a sequence similar to the binding site 1 for the nodule trans-acting factor Nat2 were identified. From Southern blot data and from sequence analysis of genomic PCR fragments, the presence of a VfENOD-GRP3 gene family was inferred. By PCR experiments using sequence-specific primers and DNA of microisolated chromosomes as a template, this family was located on the long arm of chromosome I.

摘要

从蚕豆根瘤cDNA文库中分离出一个根瘤特异性cDNA。由于时间进程实验显示该转录本在根瘤中早期表达,此cDNA编码一种早期结瘤素,被命名为VfENOD-GRP3。基于组织印记杂交,我们发现VfENOD-GRP3转录本在蚕豆根瘤的II-III区主要表达。编码的早期结瘤素ENOD-GRP3的特征是具有一个N端信号肽和一个C端结构域,其甘氨酸含量为31%。对VfENOD-GRP3基因组克隆的序列分析表明,信号肽和富含甘氨酸的结构域由两个独立的外显子指定。引物延伸实验确定了VfENOD-GRP3转录本的两个相邻转录起始位点。常见的结瘤素序列“AAAGAT”和“CTCTT”分别在假定的VfENOD-GRP3启动子的两条DNA链上出现了5次和3次。此外,还鉴定出三个类似于大豆lbc3基因启动子器官特异性元件的序列基序和一个类似于根瘤反式作用因子Nat2结合位点1的序列。从Southern杂交数据和基因组PCR片段的序列分析推断出VfENOD-GRP3基因家族的存在。通过使用序列特异性引物和微分离染色体DNA作为模板的PCR实验,该家族定位于第一条染色体的长臂上。

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