Corich V, Goormachtig S, Lievens S, Van Montagu M, Holsters M
Department of Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), Universiteit Gent, Belgium.
Plant Mol Biol. 1998 May;37(1):67-76. doi: 10.1023/a:1005925607793.
At the base of adventitious root primordia, located on the stem of the tropical legume Sesbania rostrata, nitrogen-fixing nodules are formed upon inoculation with the microsymbiont Azorhizobium caulinodans. This pattern of nodule development presents features of indeterminate and determinate nodules in early and later stages, respectively. A S. rostrata cDNA clone homologous to early nodulin ENOD40 genes was isolated from a cDNA library of developing stem nodules. SrENOD40-1 contained the conserved regions I and II of other ENOD40 genes. By reverse transcriptase PCR, enhanced SrENOD40-1 expression was observed in the adventitious root primordia between 4 and 8 h after inoculation with A. caulinodans. In situ hybridization showed that SrENOD40-1 transcripts, present around the central vascular bundle of the uninfected root primordia, were strongly enhanced upon induction of nodule development. De novo SrENOD40-1 expression was observed in the initiating and growing nodule primordia and around vascular bundles. When cell type specification sets in, the expression became pronounced in cells derived from the meristematic regions. In other parts of the plant, weak SrENOD40-1 expression was associated with vascular bundles and was observed in leaf and stipule primordia.
在热带豆科植物喙荚田菁茎上不定根原基的基部,接种共生微生物茎瘤固氮根瘤菌后会形成固氮根瘤。这种根瘤发育模式分别在早期和后期呈现出不定根瘤和定根瘤的特征。从发育中的茎根瘤cDNA文库中分离出一个与早期结瘤素ENOD40基因同源的喙荚田菁cDNA克隆。SrENOD40-1包含其他ENOD40基因的保守区域I和II。通过逆转录酶PCR,在接种茎瘤固氮根瘤菌后4至8小时的不定根原基中观察到SrENOD40-1表达增强。原位杂交显示,未感染根原基中央维管束周围存在的SrENOD40-1转录本在根瘤发育诱导后强烈增强。在起始和生长的根瘤原基以及维管束周围观察到SrENOD40-1的从头表达。当细胞类型特化开始时,该表达在源自分生组织区域的细胞中变得明显。在植物的其他部位,SrENOD40-1的弱表达与维管束相关,并在叶和托叶原基中观察到。