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PMID:22039214

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Citation

Liu, W, Kohlen, W, Lillo, A, Op den Camp, R, Ivanov, S, Hartog, M, Limpens, E, Jamil, M, Smaczniak, C, Kaufmann, K, Yang, WC, Hooiveld, GJ, Charnikhova, T, Bouwmeester, HJ, Bisseling, T and Geurts, R (2011) Strigolactone biosynthesis in Medicago truncatula and rice requires the symbiotic GRAS-type transcription factors NSP1 and NSP2. Plant Cell 23:3853-65

Abstract

Legume GRAS (GAI, RGA, SCR)-type transcription factors NODULATION SIGNALING PATHWAY1 (NSP1) and NSP2 are essential for rhizobium Nod factor-induced nodulation. Both proteins are considered to be Nod factor response factors regulating gene expression after symbiotic signaling. However, legume NSP1 and NSP2 can be functionally replaced by nonlegume orthologs, including rice (Oryza sativa) NSP1 and NSP2, indicating that both proteins are functionally conserved in higher plants. Here, we show that NSP1 and NSP2 are indispensable for strigolactone (SL) biosynthesis in the legume Medicago truncatula and in rice. Mutant nsp1 plants do not produce SLs, whereas in M. truncatula, NSP2 is essential for conversion of orobanchol into didehydro-orobanchol, which is the main SL produced by this species. The disturbed SL biosynthesis in nsp1 nsp2 mutant backgrounds correlates with reduced expression of DWARF27, a gene essential for SL biosynthesis. Rice and M. truncatula represent distinct phylogenetic lineages that split approximately 150 million years ago. Therefore, we conclude that regulation of SL biosynthesis by NSP1 and NSP2 is an ancestral function conserved in higher plants. NSP1 and NSP2 are single-copy genes in legumes, which implies that both proteins fulfill dual regulatory functions to control downstream targets after rhizobium-induced signaling as well as SL biosynthesis in nonsymbiotic conditions.

Links

PubMed PMC3229154 Online version:10.1105/tpc.111.089771

Keywords

Amino Acid Sequence; Carotenoids/analysis; Carotenoids/metabolism; Down-Regulation; Gene Expression Profiling; Gene Expression Regulation, Plant; Lactones/analysis; Lactones/chemistry; Lactones/metabolism; Medicago truncatula/genetics; Medicago truncatula/growth & development; Medicago truncatula/microbiology; Medicago truncatula/physiology; Molecular Sequence Data; Mutation; Oligonucleotide Array Sequence Analysis; Oryza sativa/genetics; Oryza sativa/growth & development; Oryza sativa/microbiology; Oryza sativa/physiology; Phenotype; Phylogeny; Plant Growth Regulators/metabolism; Plant Proteins/genetics; Plant Proteins/metabolism; Plant Root Nodulation; Plant Roots/genetics; Plant Roots/growth & development; Plant Roots/microbiology; Plant Roots/physiology; Sesquiterpenes/metabolism; Signal Transduction; Sinorhizobium meliloti/physiology; Symbiosis; Transcription Factors/genetics; Transcription Factors/metabolism

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

ORYSJ:Q84MQ9

GO:0042446: hormone biosynthetic process

ECO:0000315:

P

Figure 5 shows that mutants that have >90% knock down in NSP1 have reduced strigolactone (a plant hormome) production.

complete
CACAO 5474

ORYSJ:Q84MQ9

GO:2000032: regulation of secondary shoot formation

ECO:0000315:

P

Figure 5c shows that plants that had a >90% knockdown in NSP1 had an increased number of tillers (secondary shoots).

complete
CACAO 5475

ORYSJ:Q84MQ9

involved_in

GO:0042446: hormone biosynthetic process

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

ORYSJ:Q84MQ9

involved_in

GO:2000032: regulation of secondary shoot formation

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete


See also

References

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