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研究转基因苜蓿中早期结瘤素基因ENOD40的表达以及结瘤因子和细胞分裂素对其的诱导作用。

Studying early nodulin gene ENOD40 expression and induction by nodulation factor and cytokinin in transgenic alfalfa.

作者信息

Fang Y, Hirsch A M

机构信息

Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles 90095-1606, USA.

出版信息

Plant Physiol. 1998 Jan;116(1):53-68. doi: 10.1104/pp.116.1.53.

Abstract

ENOD40, an early nodulin gene, is expressed following inoculation with Rhizobium meliloti or by adding R. meliloti-produced nodulation (Nod) factors or the plant hormone cytokinin to uninoculated roots. We isolated two MsENOD40 clones, designated MsENOD40-1 and MsENOD40-2, with distinct promoters from an alfalfa (Medicago sativa cv Chief) genomic library. The promoters were fused to the reporter gene uidA (gus), and the constructs were introduced into alfalfa. We observed that the MsENOD40-1 construct was expressed almost exclusively under symbiotic conditions. The MsENOD40-2 construct was transcribed under both symbiotic and nonsymbiotic conditions and in nonnodular and nodular tissues. Both MsENOD40 promoter-gus constructs were similarly expressed as nodules developed, and both were expressed in roots treated with 6-benzylaminopurine or purified Nod factor. However, no blue color was detected in nodule-like structures induced by the auxin transport inhibitor N-1-(naphthyl)phthalamic acid on roots of plants containing the MsENOD40-1 promoter construct, whereas pseudonodules from plants containing the MsENOD40-2 promoter construct stained blue. A 616-bp region at the distal 5' end of the promoter is important for proper spatial expression of MsENOD40 in nodules and also for Nod-factor and cytokinin-induced expression.

摘要

ENOD40是一种早期结瘤素基因,在接种苜蓿根瘤菌后,或者向未接种的根中添加苜蓿根瘤菌产生的结瘤(Nod)因子或植物激素细胞分裂素后表达。我们从苜蓿(Medicago sativa cv Chief)基因组文库中分离出两个MsENOD40克隆,命名为MsENOD40-1和MsENOD40-2,它们具有不同的启动子。将这些启动子与报告基因uidA(gus)融合,并将构建体导入苜蓿。我们观察到,MsENOD40-1构建体几乎只在共生条件下表达。MsENOD40-2构建体在共生和非共生条件下以及在非根瘤和根瘤组织中都能转录。随着根瘤的发育,两个MsENOD40启动子-gus构建体的表达情况相似,并且在经6-苄基氨基嘌呤或纯化的Nod因子处理的根中都有表达。然而,在用生长素运输抑制剂N-1-(萘基)邻苯二甲酸处理含有MsENOD40-1启动子构建体的植物的根时,诱导形成的类根瘤结构中未检测到蓝色,而含有MsENOD40-2启动子构建体的植物形成的假根瘤被染成蓝色。启动子5'端远端的一个616 bp区域对于MsENOD40在根瘤中的正确空间表达以及对Nod因子和细胞分裂素诱导的表达都很重要。

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