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解析调控蒺藜苜蓿根瘤自调控过程中涉及的新分子调控因子。

Unraveling new molecular players involved in the autoregulation of nodulation in Medicago truncatula.

机构信息

Institute of Plant Sciences-Paris Saclay (IPS2), Centre National de la Recherche Scientifique, Université Paris-Sud, Université Paris-Diderot, Université d'Evry, Institut National de la Recherche Agronomique, Université Paris-Saclay, Gif-sur-Yvette, France.

Department of Plant Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.

出版信息

J Exp Bot. 2019 Feb 20;70(4):1407-1417. doi: 10.1093/jxb/ery465.

DOI:10.1093/jxb/ery465
PMID:30753553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6382332/
Abstract

The number of legume root nodules resulting from a symbiosis with rhizobia is tightly controlled by the plant. Certain members of the CLAVATA3/Embryo Surrounding Region (CLE) peptide family, specifically MtCLE12 and MtCLE13 in Medicago truncatula, act in the systemic autoregulation of nodulation (AON) pathway that negatively regulates the number of nodules. Little is known about the molecular pathways that operate downstream of the AON-related CLE peptides. Here, by means of a transcriptome analysis, we show that roots ectopically expressing MtCLE13 deregulate only a limited number of genes, including three down-regulated genes encoding lysin motif receptor-like kinases (LysM-RLKs), among which are the nodulation factor (NF) receptor NF Perception gene (NFP) and two up-regulated genes, MtTML1 and MtTML2, encoding Too Much Love (TML)-related Kelch-repeat containing F-box proteins. The observed deregulation was specific for the ectopic expression of nodulation-related MtCLE genes and depended on the Super Numeric Nodules (SUNN) AON RLK. Moreover, overexpression and silencing of these two MtTML genes demonstrated that they play a role in the negative regulation of nodule numbers. Hence, the identified MtTML genes are the functional counterpart of the Lotus japonicus TML gene shown to be central in the AON pathway. Additionally, we propose that the down-regulation of a subset of LysM-RLK-encoding genes, among which is NFP, might contribute to the restriction of further nodulation once the first nodules have been formed.

摘要

豆科植物根瘤的数量与根瘤菌的共生受到植物的严格控制。拟南芥 CLAVATA3/胚周围区域 (CLE) 肽家族的某些成员,特别是蒺藜苜蓿中的 MtCLE12 和 MtCLE13,在负调控根瘤数量的系统自动调节 (AON) 途径中起作用。关于 AON 相关 CLE 肽下游的分子途径知之甚少。在这里,我们通过转录组分析表明,异位表达 MtCLE13 的根仅下调了少数基因,包括三个下调的编码丝氨酸蛋白酶样受体样激酶 (LysM-RLK) 的基因,其中包括结瘤因子 (NF) 受体 NF 感知基因 (NFP) 和两个上调的基因 MtTML1 和 MtTML2,编码与 Too Much Love (TML) 相关的 Kelch-repeat 含有 F-box 蛋白。观察到的基因失调是结瘤相关 MtCLE 基因异位表达所特有的,并且依赖于 Super Numeric Nodules (SUNN) AON RLK。此外,这两个 MtTML 基因的过表达和沉默表明它们在负调控根瘤数量中发挥作用。因此,鉴定出的 MtTML 基因是拟南芥 TML 基因的功能对应物,该基因被证明在 AON 途径中起核心作用。此外,我们提出,一组 LysM-RLK 编码基因的下调,其中包括 NFP,可能有助于限制一旦形成第一个根瘤后进一步的结瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/dbce9338cfa2/exbotj_ery465_f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/09c7bcd2f56c/exbotj_ery465_f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/81dd853da712/exbotj_ery465_f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/9527c072b163/exbotj_ery465_f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/a42f06bf8708/exbotj_ery465_f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/5147c390585c/exbotj_ery465_f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/a31f8b2cfd92/exbotj_ery465_f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/dbce9338cfa2/exbotj_ery465_f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/09c7bcd2f56c/exbotj_ery465_f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/81dd853da712/exbotj_ery465_f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/9527c072b163/exbotj_ery465_f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/a42f06bf8708/exbotj_ery465_f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/5147c390585c/exbotj_ery465_f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/a31f8b2cfd92/exbotj_ery465_f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc19/6382332/dbce9338cfa2/exbotj_ery465_f0007.jpg

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