Symbiotic Rhizobia Bacteria Trigger a Change in Localization and Dynamics of the Medicago truncatula Receptor Kinase LYK3
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作者:
Haney, Cara H.
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Stanford Univ, Dept Biol, Stanford, CA 94305 USAStanford Univ, Dept Biol, Stanford, CA 94305 USA
Haney, Cara H.
[1
]
Riely, Brendan K.
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Univ Calif Davis, Dept Plant Pathol, Davis, CA 95616 USAStanford Univ, Dept Biol, Stanford, CA 94305 USA
Riely, Brendan K.
[2
]
Tricoli, David M.
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Univ Calif Davis, Dept Plant Pathol, Davis, CA 95616 USA
Univ Calif Davis, Ralph M Parsons Fdn Plant Transformat Facil, Davis, CA 95616 USAStanford Univ, Dept Biol, Stanford, CA 94305 USA
Tricoli, David M.
[2
,3
]
Cook, Doug R.
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Univ Calif Davis, Dept Plant Pathol, Davis, CA 95616 USAStanford Univ, Dept Biol, Stanford, CA 94305 USA
Cook, Doug R.
[2
]
Ehrhardt, David W.
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Stanford Univ, Dept Biol, Stanford, CA 94305 USA
Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USAStanford Univ, Dept Biol, Stanford, CA 94305 USA
Ehrhardt, David W.
[1
,4
]
Long, Sharon R.
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Stanford Univ, Dept Biol, Stanford, CA 94305 USAStanford Univ, Dept Biol, Stanford, CA 94305 USA
Long, Sharon R.
[1
]
机构:
[1] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[2] Univ Calif Davis, Dept Plant Pathol, Davis, CA 95616 USA
[3] Univ Calif Davis, Ralph M Parsons Fdn Plant Transformat Facil, Davis, CA 95616 USA
[4] Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
To form nitrogen-fixing symbioses, legume plants recognize a bacterial signal, Nod Factor (NF). The legume Medicago truncatula has two predicted NF receptors that direct separate downstream responses to its symbiont Sinorhizobium meliloti. NOD FACTOR PERCEPTION encodes a putative low-stringency receptor that is responsible for calcium spiking and transcriptional responses. LYSIN MOTIF RECEPTOR-LIKE KINASE3 (LYK3) encodes a putative high-stringency receptor that mediates bacterial infection. We localized green fluorescent protein (GFP)-tagged LYK3 in M. truncatula and found that it has a punctate distribution at the cell periphery consistent with a plasma membrane or membrane-tethered vesicle localization. In buffer-treated control roots, LYK3:GFP puncta are dynamic. After inoculation with compatible S. meliloti, LYK3:GFP puncta are relatively stable. We show that increased LYK3:GFP stability depends on bacterial NF and NF structure but that NF is not sufficient for the change in LYK3:GFP dynamics. In uninoculated root hairs, LYK3:GFP has little codistribution with mCherry-tagged FLOTILLIN4 (FLOT4), another punctate plasma membrane-associated protein required for infection. In inoculated root hairs, we observed an increase in FLOT4:mCherry and LYK3:GFP colocalization; both proteins localize to positionally stable puncta. We also demonstrate that the localization of tagged FLOT4 is altered in plants carrying a mutation that inactivates the kinase domain of LYK3. Our work indicates that LYK3 protein localization and dynamics are altered in response to symbiotic bacteria.