Scheres B, McKhann H I, Zalensky A, Löbler M, Bisseling T, Hirsch A M
Department of Molecular Biology, Agricultural University, P.O. Box 8091, 6700 EP Wageningen, The Netherlands.
Plant Physiol. 1992 Dec;100(4):1649-55. doi: 10.1104/pp.100.4.1649.
A number of early nodulin genes are expressed in specific cell types as pea (Pisum sativum) root nodules develop. The Pisum sativum early nodulin PsENOD2 is detected only in the uninfected cells of the nodule parenchyma, whereas PsENOD12 is expressed at two spatially removed sites: in root hairs and adjacent cortical cells, both of which can be invaded by Rhizobium entering through infection threads, and in derivatives of newly divided root inner cortical cells that establish the nodule primordium. We tested whether Rhizobium infection is required for triggering PsENOD12 gene expression by inducing nodule-like structures on Afghanistan pea roots with the auxin transport inhibitor N-(1-naphthyl)phthalamic acid (NPA). These nodule-like structures lack infection threads but resemble Rhizobium-induced nodules in other aspects. For one, both PsENOD2 and PsENOD12 transcripts were detected in these structures. PsENOD2 mRNA was localized by in situ hybridization to a zone equivalent to the nodule parenchyma of Rhizobium-induced nodules, whereas PsENOD12 transcripts were detected in a group of cells comparable to the nodule primordium of developing nodules. In addition, PsENOD12 mRNA was detected in uninfected root hairs 48 h after NPA treatment. These results indicate that infection is not a trigger for PsENOD12 gene expression in Afghanistan pea and rather suggest that the expression of the PsENOD2 and PsENOD12 genes is correlated with the differentiation of specific cell types in the developing nodule.
随着豌豆(Pisum sativum)根瘤的发育,一些早期结瘤素基因在特定细胞类型中表达。豌豆早期结瘤素PsENOD2仅在根瘤薄壁组织的未感染细胞中检测到,而PsENOD12在两个空间上分离的部位表达:在根毛和相邻的皮层细胞中,这两个部位都可被通过感染丝进入的根瘤菌侵入,以及在形成根瘤原基的新分裂的根内皮层细胞的衍生物中。我们通过用生长素运输抑制剂N-(1-萘基)邻苯二甲酸(NPA)诱导阿富汗豌豆根上形成类根瘤结构,来测试根瘤菌感染是否是触发PsENOD12基因表达所必需的。这些类根瘤结构缺乏感染丝,但在其他方面类似于根瘤菌诱导的根瘤。一方面,在这些结构中检测到了PsENOD2和PsENOD12转录本。通过原位杂交将PsENOD2 mRNA定位到与根瘤菌诱导的根瘤的根瘤薄壁组织相当的区域,而在一组与发育中的根瘤的根瘤原基相当的细胞中检测到了PsENOD12转录本。此外,在NPA处理48小时后,在未感染的根毛中检测到了PsENOD12 mRNA。这些结果表明,感染不是阿富汗豌豆中PsENOD12基因表达的触发因素,而是表明PsENOD2和PsENOD12基因的表达与发育中的根瘤中特定细胞类型的分化相关。