Minami E, Kouchi H, Cohn J R, Ogawa T, Stacey G
Department of Microbiology, University of Tennessee, Knoxville 37996-0845, USA.
Plant J. 1996 Jul;10(1):23-32. doi: 10.1046/j.1365-313x.1996.10010023.x.
The lipo-chitin (LCO) nodulation signal (nod signal) purified from Bradyrhizobium japonicum induced nodule primordia on soybean (i.e. Glycine soja) roots. These primordia were characterized by a bifurcated vascular connection, cortical cell division, and the accumulation of mRNA of the early nodulin gene, ENOD40. A chemically synthesized LCO identical in structure to the Nod signal purified from B. japonicum cultures showed the same activity when inoculated on to soybean roots. Surprisingly, synthetic LCO or chitin pentamer, inactive in inducing root hair curling (HAD) or cortical cell division (NOI) in G. soja, induced the transient accumulation of ENOD40 mRNA. In roots inoculated with such LCO, ENOD40 mRNA was abundant at 40 h after inoculation but decreased to the background levels 6 days after inoculation. In contrast, nod signals active in inducing HAD and NOI induced high levels of ENOD40 accumulation at 40 h and 6 days after inoculation. In situ hybridization analysis showed that ENOD40 mRNA accumulated in the pericycle of the vascular bundle at 24 h after root inoculation with nod signal. At 6 days post-inoculation with nod signal, ENOD40 expression was seen in dividing subepidermal cortical cells. These results provide morphological and molecular evidence that nodule induction in soybean in response to purified or synthetic nod signal is similar, if not identical, to nodule formation induced by bacterial inoculation. Surprisingly, ENOD40 mRNA accumulation occurs in response to non-specific chitin signals. This suggests that, in the case of ENOD40, nodulation specificity is not determined at the level of initial gene expression.
从日本慢生根瘤菌中纯化得到的脂壳寡糖(LCO)结瘤信号(结瘤信号)可诱导大豆(即野生大豆)根上形成根瘤原基。这些原基的特征是具有分叉的维管连接、皮层细胞分裂以及早期结瘤素基因ENOD40的mRNA积累。一种化学合成的LCO,其结构与从日本慢生根瘤菌培养物中纯化得到的结瘤信号相同,接种到大豆根上时表现出相同的活性。令人惊讶的是,合成的LCO或几丁质五聚体,在诱导野生大豆根毛卷曲(HAD)或皮层细胞分裂(NOI)方面无活性,但却能诱导ENOD40 mRNA的瞬时积累。在用这种LCO接种的根中,接种后40小时ENOD40 mRNA丰富,但接种6天后降至背景水平。相比之下,在诱导HAD和NOI方面有活性的结瘤信号在接种后40小时和6天诱导ENOD40高水平积累。原位杂交分析表明,用结瘤信号接种根后24小时,ENOD40 mRNA在维管束的中柱鞘中积累。在接种结瘤信号6天后,在分裂的表皮下皮层细胞中可见ENOD40表达。这些结果提供了形态学和分子证据,表明大豆对纯化或合成结瘤信号的结瘤诱导与细菌接种诱导的结瘤形成相似,即使不完全相同。令人惊讶的是,ENOD40 mRNA积累是对非特异性几丁质信号的响应。这表明,就ENOD40而言,结瘤特异性不是在初始基因表达水平上决定的。