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脂壳寡糖结瘤信号对大豆根中早期结瘤素ENOD2诱导的协同作用。

Cooperative action of lipo-chitin nodulation signals on the induction of the early nodulin, ENOD2, in soybean roots.

作者信息

Minami E, Kouchi H, Carlson R W, Cohn J R, Kolli V K, Day R B, Ogawa T, Stacey G

机构信息

Dept. of Microbiology, University of Tennessee, Knoxville 37996-0845, USA.

出版信息

Mol Plant Microbe Interact. 1996 Sep;9(7):574-83. doi: 10.1094/mpmi-9-0574.

Abstract

Various lipo-chitin molecules were tested for their ability to induce the expression of the early nodulin, ENOD2, in Glycine soja roots. When inoculated separately onto G. soja roots, LCO-V (C18:1 delta 11,Mefuc), LCO-V (C18:1 delta 9,Mefuc), LCO-V (C16:0,Mefuc), and LCO-IV (C16:0) were unable to induce ENOD2 expression, even though these compounds had previously been shown to induce root hair curling, the formation of nodule-like primordia, and induction of the early nodulin, ENOD40. ENOD2 expression, however, was induced when any two of these molecules were inoculated in combination. Thus, the lipo-chitin nodulation signals appear to act cooperatively to induce ENOD2 expression. B. japonicum strains USDA110 and USDA135 and B. elkanii strain USDA61, all symbionts of soybean, were found to produce at least two distinct nod signals ([i.e., NodBj-V[C18:1,Mefuc] and NodBj-V[C16:0,Mefuc]). These two compounds were mixed in various ratios and tested for their ability to induce ENOD2 expression. The results indicate that the former compound must be present in equivalent or excess amount in order to obtain maximum ENOD2 expression. Additional nonspecific LCOs (e.g., LCO-IV[C16:2 delta 2,9; SO3]), incapable of inducing root hair curling or cortical cell division, were tested in combination with the four active LCOs listed above. It was found that any combination of one active LCO with a nonspecific LCO was sufficient to induce ENOD2 mRNA expression. The ENOD2 mRNA expression pattern detected by in situ hybridization closely resembled that found in bacterial-induced nodules with expression detected in cortical cells between primary and secondary meristems and around the vascular strands. These data demonstrate that the cooperative action of at least two LCO nodulation signals leads to a greater progression of nodule ontogeny as demonstrated by the expression of ENOD2, a marker gene for the differentiation of nodule parenchyma.

摘要

对多种脂几丁质分子诱导野生大豆根中早期结瘤素ENOD2表达的能力进行了测试。当分别接种到野生大豆根上时,LCO-V(C18:1 Δ11,甲基岩藻糖)、LCO-V(C18:1 Δ9,甲基岩藻糖)、LCO-V(C16:0,甲基岩藻糖)和LCO-IV(C16:0)均无法诱导ENOD2表达,尽管这些化合物此前已被证明能诱导根毛卷曲、形成类根瘤原基以及诱导早期结瘤素ENOD40。然而,当将这些分子中的任意两种组合接种时,就能诱导ENOD2表达。因此,脂几丁质结瘤信号似乎协同作用来诱导ENOD2表达。大豆的共生菌日本慢生根瘤菌菌株USDA110和USDA135以及埃氏慢生根瘤菌菌株USDA61被发现能产生至少两种不同的结瘤信号(即NodBj-V[C18:1,甲基岩藻糖]和NodBj-V[C16:0,甲基岩藻糖])。将这两种化合物以不同比例混合,并测试它们诱导ENOD2表达的能力。结果表明,为了获得最大的ENOD2表达,前一种化合物必须以等量或过量存在。将无法诱导根毛卷曲或皮层细胞分裂的其他非特异性脂壳寡糖(如LCO-IV[C16:2 Δ2,9;SO3])与上述四种活性脂壳寡糖组合进行测试。发现一种活性脂壳寡糖与一种非特异性脂壳寡糖的任何组合都足以诱导ENOD2 mRNA表达。通过原位杂交检测到的ENOD2 mRNA表达模式与在细菌诱导的根瘤中发现的模式非常相似,在初生和次生分生组织之间的皮层细胞以及维管束周围都检测到了表达。这些数据表明,至少两种脂壳寡糖结瘤信号的协同作用导致结瘤个体发育有更大进展,如结瘤薄壁组织分化的标记基因ENOD2的表达所示。

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