截形苜蓿
生物
根瘤菌
莲藕
突变体
根瘤菌
固氮
共生
细胞生物学
莲花
拟南芥
基因
根瘤
植物
遗传学
细菌
作者
Senjuti Sinharoy,Chengwu Liu,Andrew Breakspear,Dian Guan,Sarah Shailes,Jin Nakashima,Shulan Zhang,Jiangqi Wen,Ivone Torres‐Jerez,Giles Oldroyd,Jeremy D. Murray,Michael K. Udvardi
出处
期刊:Plant Physiology
[Oxford University Press]
日期:2016-02-16
卷期号:170 (4): 2204-2217
被引量:54
摘要
The symbiosis between leguminous plants and soil rhizobia culminates in the formation of nitrogen-fixing organs called nodules that support plant growth. Two Medicago truncatula Tnt1-insertion mutants were identified that produced small nodules, which were unable to fix nitrogen effectively due to ineffective rhizobial colonization. The gene underlying this phenotype was found to encode a protein containing a putative membrane-localized domain of unknown function (DUF21) and a cystathionine-β-synthase domain. The cbs 1 mutants had defective infection threads that were sometimes devoid of rhizobia and formed small nodules with greatly reduced numbers of symbiosomes. We studied the expression of the gene, designated M. truncatula Cystathionine-β-Synthase-like1 (MtCBS 1), using a promoter-β-glucuronidase gene fusion, which revealed expression in infected root hair cells, developing nodules, and in the invasion zone of mature nodules. An MtCBS1-GFP fusion protein localized itself to the infection thread and symbiosomes. Nodulation factor-induced Ca2+ responses were observed in the cbs 1 mutant, indicating that MtCBS1 acts downstream of nodulation factor signaling. MtCBS 1 expression occurred exclusively during Medicago-rhizobium symbiosis. Induction of MtCBS 1 expression during symbiosis was found to be dependent on Nodule Inception (NIN), a key transcription factor that controls both rhizobial infection and nodule organogenesis. Interestingly, the closest homolog of MtCBS 1, MtCBS 2, was specifically induced in mycorrhizal roots, suggesting common infection mechanisms in nodulation and mycorrhization. Related proteins in Arabidopsis have been implicated in cell wall maturation, suggesting a potential role for CBS1 in the formation of the infection thread wall.
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