Australian Research Council Centre of Excellence for Integrative Legume Research, Plant Science Division, Research School of Biology, The Australian National University, Canberra 0200, Australia.
New Phytol. 2011 Jun;190(4):865-874. doi: 10.1111/j.1469-8137.2011.03738.x. Epub 2011 Apr 20.
A subset of CLAVATA3/endosperm-surrounding region-related (CLE) peptides are involved in autoregulation of nodulation (AON) in Medicago truncatula (e.g. MtCLE12 and MtCLE13). However, their linkage to other components of the AON pathways downstream of the shoot-derived inhibitor (SDI) is not understood. We have ectopically expressed the putative peptide ligand encoding genes MtCLE12 and MtCLE13 in M. truncatula which abolished nodulation completely in wild-type roots but not in the supernodulating null mutant sunn-4. Further, root growth inhibition was detected when MtCLE12 was ectopically expressed in wild-type roots or synthetic CLE12 peptide was applied exogenously. To identify downstream genes, roots of wild-type and sunn-4 mutant overexpressing MtCLE12 were used for quantitative gene expression analysis. We found that, in 35S:MtCLE12 roots, NODULE INCEPTION (NIN, a central regulator of nodulation) was down-regulated, whereas MtEFD (ethylene response factor required for nodule differentiation) and MtRR8 (a type-A response regulator thought to be involved in the negative regulation of cytokinin signaling), were up-regulated. Moreover, we found that the up-regulation of MtEFD and MtRR8 caused by overexpressing MtCLE12 is SUNN-dependent. Hence, our data link for the first time the pathways for Nod factor signaling, cytokinin perception and AON.
一组 CLAVATA3/胚乳周围区域相关 (CLE) 肽参与了 Medicago truncatula 中结瘤的自动调节 (AON) (例如 MtCLE12 和 MtCLE13)。然而,它们与 SDI 下游 AON 途径的其他成分的联系尚不清楚。我们在 M. truncatula 中外源表达了假定的肽配体编码基因 MtCLE12 和 MtCLE13,这完全消除了野生型根中的结瘤,但在超级结瘤突变体 sunn-4 中没有消除。此外,当 MtCLE12 在野生型根中外源表达或合成 CLE12 肽外施时,检测到根生长抑制。为了鉴定下游基因,我们使用野生型和 sunn-4 突变体过量表达 MtCLE12 的根进行了定量基因表达分析。我们发现,在 35S:MtCLE12 根中,结瘤起始基因 (NIN,结瘤的中央调节剂) 下调,而 MtEFD(乙烯反应因子,是结瘤分化所必需的)和 MtRR8(一种 A 型反应调节因子,被认为参与细胞分裂素信号的负调节)上调。此外,我们发现过量表达 MtCLE12 引起的 MtEFD 和 MtRR8 的上调依赖于 sunn。因此,我们的数据首次将 Nod 因子信号、细胞分裂素感知和 AON 途径联系起来。