Chen R, Silver DL
Michigan State University Department of Energy Plant Research Laboratory, East Lansing, Michigan 48824-1312, USA.
Plant Cell. 1998 Oct;10(10):1585-602. doi: 10.1105/tpc.10.10.1585.
The early nodulin Enod2 gene encodes a putative hydroxyproline-rich cell wall protein and is expressed exclusively in the nodule parenchyma cell layer. The latter finding suggests that the Enod2 protein may contribute to the special morphological features of the nodule parenchyma and to the creation of an oxygen diffusion barrier. The Enod2 gene of the stem-nodulating legume Sesbania rostrata (SrEnod2) is induced specifically in roots by the plant hormone cytokinin, and this induction occurs at a post-transcriptional level. Here, we characterize the cis determinant(s) in the SrEnod2 locus responsible for nodule parenchyma-specific expression and show that the 3' untranslated region (UTR) of the SrEnod2 gene is both required and sufficient for directing chimeric reporter gene expression in the nodule parenchyma of transgenic Lotus corniculatus plants. Moreover, we show that the SrEnod2 3' UTR does not act as a tissue-specific enhancer element. By conducting a detailed deletion analysis of the 5' and 3' SrEnod2 regions, we delimited the minimal promoter of the SrEnod2 gene, and it appears that the 5' flanking sequences are not essential for nodule parenchyma-specific expression. This finding is in contrast with the report that the 5' upstream region of the soybean Enod2 gene directs nodule parenchyma-specific expression, indicating that different mechanisms may be involved in regulating the expression of these two genes. We definitively demonstrate that the cis element(s) for tissue-specific expression is located within the 3' UTR of a plant nuclear gene.
早期结瘤素Enod2基因编码一种假定的富含羟脯氨酸的细胞壁蛋白,且仅在根瘤薄壁细胞层中表达。后一发现表明,Enod2蛋白可能有助于根瘤薄壁细胞的特殊形态特征以及形成氧气扩散屏障。茎瘤豆类植物喙荚田菁(Sesbania rostrata)的Enod2基因(SrEnod2)受植物激素细胞分裂素的特异性诱导,且这种诱导发生在转录后水平。在此,我们鉴定了SrEnod2基因座中负责根瘤薄壁细胞特异性表达的顺式作用元件,并表明SrEnod2基因的3'非翻译区(UTR)对于指导嵌合报告基因在转基因百脉根(Lotus corniculatus)植物的根瘤薄壁细胞中表达既是必需的也是充分的。此外,我们表明SrEnod2的3'UTR并不作为组织特异性增强子元件起作用。通过对SrEnod2基因5'和3'区域进行详细的缺失分析,我们确定了SrEnod2基因的最小启动子,并且看起来5'侧翼序列对于根瘤薄壁细胞特异性表达并非必需。这一发现与关于大豆Enod2基因5'上游区域指导根瘤薄壁细胞特异性表达的报道相反,表明可能涉及不同机制来调控这两个基因的表达。我们明确证明了组织特异性表达的顺式元件位于植物核基因的3'UTR内。