Get it Sorted: A Classic Endocytic Sorting Mechanism in Mammals is Conserved in Plants[OPEN]

The plasma membrane (PM) is an exquisitely dynamic structure. It has to be, because it serves as the interface between the cell and the ever-changing environment. PM-associated signaling proteins shuttle quickly between the PM and the cell’s interior to help the organism respond to whatever comes its way. Cells employ pathways such as clathrinmediated endocytosis (CME) to selectively engulf a targetprotein in thePMandmove it into thecell asneeded tofine-tunesignaling (reviewed by Reynolds et al., 2018). In the mammalian CME pathway, PM proteins marked by specific Tyr or di-Leu motifs in their cytoplasmic tails are recognizedby the heterotetrameric adaptor protein complex2 (AP-2). AP-2 recruits lattice-like clathrin molecules, which coat the budding PMand form a cage around the cargo-packed vesicle that carries theprotein to itsdestination. Themost commonmotif, YXXF (where Y is Tyr, X is any amino acid, and F is a bulky hydrophobic residue), is recognized by the medium AP-2 subunit AP2M. Although the CME pathway plays crucial roles in modulating plant physiology, very little is knownabout howPMproteins in plants are sorted by AP-2 for CME and whether YXXF motifs are required for protein recognition. To probe this issue, Derui Liu and colleagues (Liu et al., 2020) studied CME of the brassinosteroid (BR) receptor BR INSENSITIVE1 (BRI1) in Arabidopsis (Arabidopsis thaliana), a process known to depend on clathrin and AP-2. BRsplaymultiple roles throughout theplant lifecycle (reviewed by Nolan et al., 2020). The PMpool of BRI1 controls BR signaling: Impaired endocytosis of this receptor kinase leads to constitutive BR responses. To look for interactions between BRI1 and AP-2, the authors examined the dynamics of GFP-taggedBRI1 andRFP-tagged large AP-2 subunit AP2A1 in the PM of root epidermal cells of the null mutant bri1-116. A portionofBRI1andAP2A1displayedsimilar dynamics and disappeared from the PM together. The direct interaction between BRI1 and AP2M was confirmed in vitro. The cytoplasmic domain of BRI1 contains fiveputative surface-exposedYXXF endocytic motifs. After narrowing the list to three candidates, the authors examined their functions in vivo by generating fulllengthBRI1-carryingmutations in eachmotif, C-terminally tagged the mutant proteins with mCitrine, and expressed them in the Arabidopsis bri1 null allele. All three mutant proteinscomplementedbri1.However,only plantswith a Tyr-to-Phe substitution inBRI1 (BRI1Y898F) were hypersensitive to BRs, as revealed in a hypocotyl growth assay. Unlike the other mutations, the BRI1Y898F mutation did not impair the kinase activity of BRI1. BR treatment leads to dephosphorylation of the transcription factor BES1, a commonly used indicator of BR signaling activation. Upon exogenous BR treatment, dephosphorylated BES1 accumulated at higher levels in BRI1Y898F versus BRI1 plants, confirming the hypersensitivity of theseplantstoBRs.Todeterminewhether this hypersensitivity was due to increased levels of BRI1 at the PM, mCitrine-tagged BRI1Y898F-versus-BRI1 signals at the PM of root meristem cells were examined in transgenic bri1 seedlings after treatment with cycloheximide to inhibit de novo protein synthesis. BRI1Y898F generated significantly stronger fluorescent signals at the PM than BRI1. Brefeldin A (BFA) treatment to inhibit exocytosis led to fewer and smaller BFA bodies in plants harboringBRI1Y898F versus BRI1 (see figure), indicating that endocytosis of the mutant protein was impaired. Finally, BRI1Y898F showed reduced binding to AP2M in an in vitro pull-down assay, confirming that AP2M recognizes this motif to facilitate CME. (Adapted from Liu et al. [2020], Figure 4C.)

The plasma membrane (PM) is an exquisitely dynamic structure. It has to be, because it serves as the interface between the cell and the ever-changing environment. PM-associated signaling proteins shuttle quickly between the PM and the cell's interior to help the organism respond to whatever comes its way. Cells employ pathways such as clathrinmediated endocytosis (CME) to selectively engulf a target protein in the PM and move it into the cell as needed to fine-tune signaling (reviewed by Reynolds et al., 2018). In the mammalian CME pathway, PM proteins marked by specific Tyr or di-Leu motifs in their cytoplasmic tails are recognized by the heterotetrameric adaptor protein complex-2 (AP-2). AP-2 recruits lattice-like clathrin molecules, which coat the budding PM and form a cage around the cargo-packed vesicle that carries the protein to its destination. The most common motif, YXXF (where Y is Tyr, X is any amino acid, and F is a bulky hydrophobic residue), is recognized by the medium AP-2 subunit AP2M.
Although the CME pathway plays crucial roles in modulating plant physiology, very little is known about how PM proteins in plants are sorted by AP-2 for CME and whether YXXF motifs are required for protein recognition. To probe this issue, Derui Liu and colleagues  studied CME of the brassinosteroid (BR) receptor BR INSENSITIVE1 (BRI1) in Arabidopsis (Arabidopsis thaliana), a process known to depend on clathrin and AP-2. BRs play multiple roles throughout the plant lifecycle (reviewed by Nolan et al., 2020). The PM pool of BRI1 controls BR signaling: Impaired endocytosis of this receptor kinase leads to constitutive BR responses. To look for interactions between BRI1 and AP-2, the authors examined the dynamics of GFP-tagged BRI1 and RFP-tagged large AP-2 subunit AP2A1 in the PM of root epidermal cells of the null mutant bri1-116. A portion of BRI1 and AP2A1 displayed similar dynamics and disappeared from the PM together. The direct interaction between BRI1 and AP2M was confirmed in vitro.
The cytoplasmic domain of BRI1 contains five putative surface-exposed YXXF endocytic motifs. After narrowing the list to three candidates, the authors examined their functions in vivo by generating fulllength BRI1-carrying mutations in each motif, C-terminally tagged the mutant proteins with mCitrine, and expressed them in the Arabidopsis bri1 null allele. All three mutant proteins complemented bri1. However, only plants with a Tyr-to-Phe substitution in BRI1 (BRI1 Y898F ) were hypersensitive to BRs, as revealed in a hypocotyl growth assay. Unlike the other mutations, the BRI1 Y898F mutation did not impair the kinase activity of BRI1.
BR treatment leads to dephosphorylation of the transcription factor BES1, a commonly used indicator of BR signaling activation. Upon exogenous BR treatment, dephosphorylated BES1 accumulated at higher levels in BRI1 Y898F versus BRI1 plants, confirming the hypersensitivity of these plants to BRs. To determine whether this hypersensitivity was due to increased levels of BRI1 at the PM, mCitrine-tagged BRI1 Y898F -versus-BRI1 signals at the PM of root meristem cells were examined in transgenic bri1 seedlings after treatment with cycloheximide to inhibit de novo protein synthesis. BRI1 Y898F generated significantly stronger fluorescent signals at the PM than BRI1. Brefeldin A (BFA) treatment to inhibit exocytosis led to fewer and smaller BFA bodies in plants harboring BRI1 Y898F versus BRI1 (see figure), indicating that endocytosis of the mutant protein was impaired. Finally, BRI1 Y898F showed reduced binding to AP2M in an in vitro pull-down assay, confirming that AP2M recognizes this motif to facilitate CME.
[OPEN] Articles can be viewed without a subscription. www.plantcell.org/cgi/doi/10. 1105/tpc.20.00790 As shown in the figure, disrupting the YXXF motif in BRI1 failed to fully block its internalization, raising the question of whether an additional sorting mechanism is at play. Stay tuned.

Get it Sorted: A Classic Endocytic Sorting Mechanism in Mammals is Conserved in Plants
This information is current as of January 3, 2021