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1
Nodule parenchyma-specific expression of the sesbania rostrata early nodulin gene SrEnod2 is mediated by its 3' untranslated region.喙荚田菁早期结瘤素基因SrEnod2在根瘤薄壁组织中的特异性表达由其3'非翻译区介导。
Plant Cell. 1998 Oct;10(10):1585-602. doi: 10.1105/tpc.10.10.1585.
2
The early nodulin gene SrEnod2 from Sesbania rostrata is inducible by cytokinin.来自喙荚田菁的早期结瘤素基因SrEnod2可被细胞分裂素诱导。
Plant J. 1992 Jan;2(1):117-28. doi: 10.1046/j.1365-313x.1992.t01-51-00999.x.
3
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Plant Cell. 1990 Oct;2(10):973-86. doi: 10.1105/tpc.2.10.973.
4
Conserved regulation of the soybean early nodulin ENOD2 gene promoter in determine and indeterminate transgenic root nodules.大豆早期结瘤素ENOD2基因启动子在决定型和非决定型转基因根瘤中的保守调控
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Root nodule specific gene regulation: analysis of the soybean nodulin N23 gene promoter in heterologous symbiotic systems.根瘤特异性基因调控:异源共生系统中大豆根瘤蛋白N23基因启动子的分析
Nucleic Acids Res. 1988 Jan 11;16(1):39-50. doi: 10.1093/nar/16.1.39.

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本文引用的文献

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Developmental biology of a plant-prokaryote symbiosis: the legume root nodule.植物-原核生物共生的发育生物学:豆科植物根瘤。
Science. 1990 Nov 16;250(4983):948-54. doi: 10.1126/science.250.4983.948.
2
Early nodulin genes are induced in alfalfa root outgrowths elicited by auxin transport inhibitors.早期结瘤素基因在由生长素运输抑制剂诱导的紫花苜蓿根突起中被诱导。
Proc Natl Acad Sci U S A. 1989 Feb;86(4):1244-8. doi: 10.1073/pnas.86.4.1244.
3
Identification of an essential upstream element in the nopaline synthase promoter by stable and transient assays.利用稳定和瞬时测定鉴定胭脂碱合酶启动子中的必需上游元件。
Proc Natl Acad Sci U S A. 1987 Aug;84(16):5745-9. doi: 10.1073/pnas.84.16.5745.
4
Characterization of cDNA for nodulin-75 of soybean: A gene product involved in early stages of root nodule development.大豆根瘤球蛋白 75 cDNA 的特性:一种参与根瘤发育早期阶段的基因产物。
Proc Natl Acad Sci U S A. 1987 Jul;84(13):4495-9. doi: 10.1073/pnas.84.13.4495.
5
Wound-inducible expression of a potato inhibitor II-chloramphenicol acetyltransferase gene fusion in transgenic tobacco plants.马铃薯蛋白酶抑制剂 II-氯霉素乙酰转移酶基因融合在转基因烟草植株中的诱导型表达。
Proc Natl Acad Sci U S A. 1987 Feb;84(3):744-8. doi: 10.1073/pnas.84.3.744.
6
Messenger RNA for G1 protein of French bean seeds: Cell-free translation and product characterization.菜豆种子G1蛋白的信使核糖核酸:无细胞翻译及产物特性分析
Proc Natl Acad Sci U S A. 1978 Jul;75(7):3196-200. doi: 10.1073/pnas.75.7.3196.
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On the Physiology of the Formation of Nodules on Legume Roots.关于豆科植物根上根瘤形成的生理学
Proc Natl Acad Sci U S A. 1936 Aug;22(8):511-4. doi: 10.1073/pnas.22.8.511.
8
The CaMV 35S enhancer contains at least two domains which can confer different developmental and tissue-specific expression patterns.CaMV 35S 增强子至少包含两个可以赋予不同发育和组织特异性表达模式的结构域。
EMBO J. 1989 Aug;8(8):2195-202. doi: 10.1002/j.1460-2075.1989.tb08342.x.
9
5' Analysis of the soybean leghaemoglobin lbc(3) gene: regulatory elements required for promoter activity and organ specificity.大豆血红蛋白 lbc(3)基因的 5' 分析:启动子活性和器官特异性所需的调控元件。
EMBO J. 1987 Dec 1;6(12):3565-9. doi: 10.1002/j.1460-2075.1987.tb02686.x.
10
Nodulin Gene Expression and ENOD2 Localization in Effective, Nitrogen-Fixing and Ineffective, Bacteria-Free Nodules of Alfalfa.苜蓿有效、固氮且无效、无细菌根瘤中结瘤素基因表达及ENOD2定位
Plant Cell. 1990 Oct;2(10):1009-1017. doi: 10.1105/tpc.2.10.1009.

喙荚田菁早期结瘤素基因SrEnod2在根瘤薄壁组织中的特异性表达由其3'非翻译区介导。

Nodule parenchyma-specific expression of the sesbania rostrata early nodulin gene SrEnod2 is mediated by its 3' untranslated region.

作者信息

Chen R, Silver DL

机构信息

Michigan State University Department of Energy Plant Research Laboratory, East Lansing, Michigan 48824-1312, USA.

出版信息

Plant Cell. 1998 Oct;10(10):1585-602. doi: 10.1105/tpc.10.10.1585.

DOI:10.1105/tpc.10.10.1585
PMID:9761788
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC144349/
Abstract

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.

摘要

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。