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A mutually assured destruction mechanism attenuates light signaling in Arabidopsis

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Science  06 Jun 2014:
Vol. 344, Issue 6188, pp. 1160-1164
DOI: 10.1126/science.1250778

Emerging from the shade into the light

As a growing seedling emerges into the light, it needs to shift its developmental program to grow toward the light. Signaling components that flip the switch from growth in the shade to growth in the light include phytochromes, which are sensitive to red light, and transcription factors that drive the shade-adapted pattern of development. Ni et al. now show how phosphorylation sets these signaling partners up for destruction. The signaling established by red light invokes photomorphogenesis by promoting the destruction of the photoreceptor and its signaling partner.

Science, this issue p. 1160

Abstract

After light-induced nuclear translocation, phytochrome photoreceptors interact with and induce rapid phosphorylation and degradation of basic helix-loop-helix transcription factors, such as PHYTOCHROME-INTERACTING FACTOR 3 (PIF3), to regulate gene expression. Concomitantly, this interaction triggers feedback reduction of phytochrome B (phyB) levels. Light-induced phosphorylation of PIF3 is necessary for the degradation of both proteins. We report that this PIF3 phosphorylation induces, and is necessary for, recruitment of LRB [Light-Response Bric-a-Brack/Tramtrack/Broad (BTB)] E3 ubiquitin ligases to the PIF3-phyB complex. The recruited LRBs promote concurrent polyubiqutination and degradation of both PIF3 and phyB in vivo. These data reveal a linked signal-transmission and attenuation mechanism involving mutually assured destruction of the receptor and its immediate signaling partner.

The mechanisms by which cells perceive and adapt to external signals remains an area of central interest in the biosciences. The capacity to respond rapidly and robustly to such signals is frequently coupled to a capacity to subsequently modulate the intensity of that response through feedback attenuation of the signaling process (1). Whereas the initial robust burst of signaling activity is presumably necessary for the induction of the consequent adaptational or developmental switch, unfettered prolongation of the elevated activity can be harmful to the organism. A plethora of attenuation mechanisms have been identified (1, 2). Defects in these mechanisms are under increasing scrutiny as evidence increases that they are major causes of human malignancies (3).

The initial emergence of seedlings from subterranean darkness into sunlight triggers a rapid and extensive redirection of gene expression that drives a developmental switch from skotomorphogenic to photomorphogenic development, which is observed as the production of normal green seedlings (4, 5). The red and far-red wavelengths inducing this switch are perceived by the phytochrome family of sensory photoreceptors (phyA to phyE) by virtue of a capacity to convert reversibly between biologically inactive Pr (red-absorbing) and biologically active Pfr (far-red-absorbing) conformers (6). Photoactivation of the cytoplasmically localized photoreceptors triggers their rapid translocation into the nucleus, where they interact directly with a subfamily of basic helix-loop-helix (bHLH) transcription factors, termed PIFs [Phytochrome-Interacting Factors; PIF1 to PIF8 (4, 7)]. This interaction induces multisite phosphorylation, ubiquitination, and degradation of the PIFs via the 26S proteasome system (4, 814), altering the transcription of target genes within minutes (4, 5, 15). The PIFs promote skotomorphogenic development in the dark (16), but their red-light–induced degradation represses this activity, inducing the switch to the photomorphogenic pathway (4).

In addition to their direct function in phytochrome signal transduction, the PIFs also desensitize cells to red light through negative feedback regulation of phyB levels (1719). We showed recently that Pfr-induced multisite phosphorylation of PIF3 is not only necessary for the degradation of PIF3, but also for concomitant PIF-interaction–induced degradation of phyB (8). Although there is evidence that E3 ligases assembled with COP1 are involved in ubiquitylation and degradation of phyB in a PIF-promoted manner (20), the signaling mechanism has remained unclear.

To address this question, we performed mass-spectrometric analysis of affinity-purified PIF3 to identify components associated with PIF3 in a light-dependent manner. Dark-grown seedlings transgenically expressing yellow fluorescent protein (YFP)–PIF3 were either kept in the dark or irradiated with 10 min of red light before protein extraction and affinity purification by using an antibody to green fluorescent protein (GFP). Quantitative spectral count analysis, not unexpectedly, identified all five phytochromes (phyA to phyE) specifically in the red light–treated samples (table S1). In addition, components of a Bric-a-Brack/Tramtrack/Broad (BTB)–Cullin3-type E3 ubiquitin ligase were also identified as red-light–specific, PIF3-interacting proteins in three biological replicates (table S1 and fig. S1). BTB proteins are substrate-specific proteins that bridge target proteins to Cullin3 for ubiquitin ligation (21, 22). The two highly conserved BTB proteins [Light-Response-BTB1 (LRB1) and LRB2] identified here were shown previously to be nuclear-localized and required genetically for proteasome-mediated phyB protein degradation in the light, but whether the involvement is direct or indirect was not determined (23). A third LRB homolog (LRB3) was not detected in our mass spectrometric analysis, possibly because of the lower expression level than those of the other two (23).

To further investigate the light-dependent interaction of PIF3 with the LRBs in vivo, we generated transgenic lines expressing both PIF3:MYC and YFP:LRB2. Immunoprecipitation using YFP:LRB2 as bait showed considerably higher levels of PIF3:MYC coprecipitation from red-treated than dark-control seedlings (Fig. 1A). The red-treated samples also displayed enrichment of the mobility-shifted forms of PIF3:MYC in the immunoprecipitates compared with the input (Fig. 1A), suggesting preferential binding of in vivo–phosphorylated PIF3 to the LRB protein. Together with previous evidence that red light induces LRB-Cullin3 interaction in vivo (23), our present findings indicate that this interaction is promoted by light-induced binding of phospho-PIF3 to the LRBs.

Fig. 1 Light-induced phosphorylation of PIF3 promotes interaction with Cullin E3-ligase substrate-recognition subunit LRB2.

(A) Light induces LRB2 and PIF3 interaction in vivo. Dark-grown seedlings from either PIF3:MYC or PIF3:MYC/YFP:LRB2 double-transgenic lines were pretreated with MG132 then either kept in the dark (Dk) or irradiated with a pulse of red light (Rp) before protein extraction and coimmunoprecipitation (Co-IP) with an antibody to GFP. The proteins were analyzed by means of Western blot with antibody either to MYC (Prey, top and middle) or to GFP (Bait, bottom). (B to D) Phosphorylation or phosphomimic mutations of the light-induced phosphosite residues in PIF3 promote its association with LRB2 in vitro. In (B) and (C), in vitro–expressed recombinant LRB2 or YFP-control (Bait) proteins were precipitated with a MYC antibody then incubated with normal [wild-type (WT)] PIF3 or the indicated light-induced–phosphosite mutant variants (A6, A20, D6, and D19) of PIF3 (Prey). Bait and prey proteins were detected by means of Western blot with antibody to MYC and to His, respectively. All proteins were expressed in Hela cell lysate. A, Ser/Thr to Ala substitutions; D, Ser/Thr to Asp substitutions; A6/D6, PIF3 with substitutions in the six strongly light-induced phosphosite residues (fig. S4A) (8); A20/D19, PIF3 with substitutions in the majority of the light-induced phosphosite residues. Co-IP products were treated with alkaline phosphatase (CIAP) in (B). (D) PIF3-A6, PIF3-WT, or PIF3-D6 expressed in Hela cell lysates were either treated (+) or not (–) with CIAP or with heat-inactivated CIAP before Western blot analysis with antibody to His. (E) High-affinity interaction of LRB2 and PIF3 in vitro requires multisite phosphorylation of PIF3. Immunoprecipitations and Western blots are as in (C). PIF3 mutant-variant substitutions are D1, S88D; D3, S58/S88/S102D. All S to A or D substitutions are provided in fig. S4A.

In vitro pulldown assays with recombinant LRB2:MYC as bait were also performed to further probe the molecular mechanism of the interaction with PIF3. Because phyB does not display autonomous light-activated protein kinase activity toward PIF3 in our hands, and no other kinase has been identified, we examined the LRB-binding behavior of a set of mutant PIF3 variants. Previously, using mass spectrometric analysis and transgenic expression of targeted missense mutants of PIF3, we identified 20 light-induced phosphorylated residues in the protein that are functionally necessary for its rapid degradation in vivo (8). When expressed in a Hela cell lysate, the phospho-dead PIF3 mutant protein (A20) showed no apparent binding to LRB2, whereas PIF3 with phospho-mimic mutations in the majority of the light-induced residues (D19), or simply the six most strongly light-induced residues (D6), exhibited high binding affinity toward LRB2 (Fig. 1B). The absence of binding to PIF3-A6 and YFP-MYC further supports the specificity of phosphorylation-dependent binding of LRB2 to PIF3 (Fig. 1C). The in vitro–expressed wild-type PIF3 intrinsically displayed multiple bands, which is reminiscent of the pattern from light-treated seedlings, and only the slower migrating form showed high affinity for LRB2 through coimmunoprecipitation (Fig. 1, B and C). Moreover, the slower migrating band of wild-type PIF3 was sensitive to alkaline phosphatase treatment (Fig. 1, B and D). These results suggest that recombinant wild-type PIF3 expressed in Hela cell lysates is phosphorylated by an unknown kinase in the lysate. Moreover, it appears that one or more of the strongly light-induced sites (8) in PIF3 is phosphorylated by this kinase because the PIF3-A6 variant, mutated at six of these sites, did not have a similarly slower migrating form (Fig. 1, C and D). In addition, in vitro pulldown assays with LRB2 as prey also indicated that PIF3-WT, D6, and D19, but not A20, bind LRB2 with high affinity (fig. S2) and that both LRB1 and LRB3 are able to bind PIF3-D6 with high affinity in vitro, similarly to LRB2 (fig. S3).

Because the six most strongly light-induced phosphosites in PIF3 are predominantly responsible for rapid degradation in vivo (8), we tested here whether binding to LRB2 in vitro also requires these multiple phospho-sites. Phosphomimic substitutions in individual (variants 1, D1, or 3) or three (variants 4 or D3) of these sites were introduced into the PIF3-A6 sequence (fig. S4A). In vitro pulldown assays showed that none of these mutant variants has LRB2 binding affinity comparable with that of PIF3-D6 (Fig. 1E and fig. S4B), suggesting that high-affinity binding to LRB2 requires between three and six light-induced phosphosites in PIF3. In addition, PIF3-D6 showed relatively low binding to either the N- or C- terminal domain of LRB2 (fig. S5B), suggesting that determinants in both domains are required for its strong binding to PIF3. These data favor the model that the cooperative action of multiple low-affinity sites between PIF3 and LRBs enable light-induced degradation of PIF3, similar to that proposed for yeast Sic1 degradation (24).

Because light-induced phosphorylation of PIF3 is also required for its negative feedback-regulation of phyB levels, despite not being required for phyB-PIF3 binding per se (8), we examined the possibility that phosphorylated PIF3 bridges the interaction of LRBs and phyB-Pfr in vivo. Pull-down assays from seedling extracts with YFP:LRB2 as bait showed light-dependent coimmunoprecipitation of phyB and PIF3 with LRB2 (Fig. 2A). In vitro binding assays indicated that LRB2 itself has some apparent affinity for phyB-Pfr alone, but that PIF3 binding enhances LRB2-phyB-Pfr association (Fig. 2, B and C).

Fig. 2 Light-induced phosphorylation of PIF3 promotes phyB-LRB2 association.

(A) Light induces phyB-LRB2 association in vivo. Proteins were extracted and immunoprecipitated by using the same lines and procedure as in Fig. 1A and then subjected to Western blot analysis by using antibody to phyB (Prey, top), to MYC (Prey, middle), or to GFP (Bait, bottom). (B) Phosphorylated PIF3 promotes phyB-LRB2 association in vitro. In vitro–expressed recombinant LRB2:MYC or YFP:MYC-control bait proteins were incubated with phyB-Pfr in the presense (+) or absence (–) of PIF3:His prey proteins and immunoprecipitated with antibody to MYC. Western blots were probed with antibody to phyB (top), to His-epitope (middle) or to MYC (bottom). (C) PIF3-D6 phosphomimic (fig. S4A) (8) promotes Pfr-dependent phyB-LRB2 association in vitro. In vitro–expressed recombinant LRB2:MYC bait protein was incubated with phyB (as Pr or Pfr) and PIF3:His [D6- or A6-mutant (fig. S4A) (8)] prey proteins and immunoprecipitated with antibody to MYC. Western blots are as in (B).

To examine the functional role of the LRBs in PIF3 and PIF3-mediated–phyB degradation, we used a set of single, double, and triple lrb mutants (23). Dark-grown seedlings of both the lrb3 single and lrb1lrb2 double mutants have normal PIF3 protein levels and normal light-induced PIF3 degradation (fig. S6A). In contrast, the lrb1lrb2lrb3 (lrb123) triple mutant exhibits a reduced rate of light-induced endogenous PIF3 degradation (Fig. 3A and fig. S6, B and C). In addition, the light-induced, slower-migrating forms of PIF3 display accumulation in the lrb123 triple mutant, compared with rapid degradation in the wild type (Fig. 3A and fig. S6B). A similar pattern was observed for a PIF3:GFP fusion protein transgenically expressed under control of the constitutive CaMV 35S promoter in the lrb123 mutant background (Fig. 3B, top and top middle, and fig. S6C), indicating that LRB regulation is exerted at the posttranslational level. Phosphatase treatment reversed the mobility shift of the accumulated slower migrating PIF3:GFP bands (Fig. 3B, bottom middle). These data indicate that PIF3 accumulates in the phosphorylated form in the light when the LRBs are mutated. The reason for the retention of higher relative levels of PIF3:GFP than endogenous PIF3 in prolonged red light (fig. S6C) is undetermined but could reflect the higher absolute levels of PIF3:GFP than endogenous PIF3.

Fig. 3 LRBs function in both PIF3 and PIF3-mediated–phyB degradation in the light.

(A) Endogenous PIF3 degradation is reduced in the lrb1lrb2lrb3 triple-mutant (lrb123) compared with Col WT seedlings in the light. Dark-grown seedlings of Col and lrb123 were irradiated with red light (R) for the period indicated before protein extraction and Western blot analysis with antibody to PIF3 (left). PIF3, unphosphorylated PIF3; PIF3-P, phosphorylated PIF3; NS, nonspecific bands. Right shows the quantification of the Western blot results from both left (blue and red curves) and fig. S6B (green and purple curves) after normalization to the Tubulin loading control. The dark PIF3 level was set as 100%. (B) PIF3:GFP accumulates in the phosphorylated form in the lrb123 triple mutant in the light. Seedling growth was as in (A). Extracted proteins were either analyzed directly (top and top middle) or after phosphatase (CIAP) treatment (bottom middle) by means of Western blot with antibody to GFP. (C) LRBs are essential for light-induced, PIF3-promoted feedback degradation of phyB. Light-induced degradation of phyB (accelerated by PIF3:GFP overexpression) is absent in the lrb123 mutant background. Dark-grown seedlings of the indicated genotypes were irradiated with 3 (R3h), 24 (R24h), or 96 (Rc96h) hours of continuous red light before protein extraction and Western blot analysis with an antibody to phyB (left and middle). Tubulin was used as a loading control. Right shows the quantification of the relative phyB/Tubulin protein levels shown to left and middle. Dark levels were set as 100%. (D) PIF3:GFP overexpression does not complement the short-hypocotyl phenotype of the lrb123 mutant in the light. Seedlings of the indicated genotypes were grown for 4 days in the dark (Dk) or continuous red light (Rc). Visible phenotypes are shown at left; hypocotyl lengths are shown at right. Error bars represent SE. (E) Endogenous PIF3 levels are strongly reduced in dark-grown seedlings of the cop1 and spa123 mutants.

We showed previously that overexpression of PIF3 markedly accelerates the rate of phyB degradation in response to light (8). This finding indicates that the absolute rate of PIF3 degradation is rate-limiting to the concurrent degradation of phyB. Because the relative rate of phyB degradation is only ~2% that of PIF3 in the wild-type seedling (8, 18, 19, 25), this observation suggests in turn that phyB is substantially more abundant than PIF3. The data for phyB in the Col wild type and the Col transgenic line overexpressing PIF3:GFP in Fig. 3C support this notion, showing the accelerated degradation of phyB in the overexpressor line. However, the light-induced degradation of phyB is absent in both the lrb12 double (fig. S6D) and lrb123 triple (Fig. 3C) mutants, with or without overexpression of PIF3:GFP, in the latter case. These data are consistent with previous evidence for the lrb mutants (23) and establish that LRB1 and LRB2 are essential for the PIF3-mediated, light-induced degradation of phyB. The absence of accelerated phyB degradation by overexpression of the PIF3-A20 variant (8) that cannot bind LRB2 (Fig. 1B) is similarly in agreement with this conclusion.

The morphogenic phenotypes of these lines are consistent with these findings. Whereas seedlings overexpressing PIF3 in wild-type Col show an etiolated-like phenotype in the light, seedlings overexpressing a similarly high or higher level of PIF3:GFP or endogenous PIF3 in the lrb123 mutant (Fig. 3, A and B, and fig. S6C) remain hypersensitive to red light, like the lrb123 mutant itself (Fig. 3D) (23). These data are in accord with the levels of phyB in these lines under prolonged red light (Fig. 3C), in which the depletion of phyB in the wild-type Col PIF3-overexpressor results in hyposensitivity to the light signal, and the stability of phyB in the lrb123 background (23) results in hypersensitivity, despite high levels of PIF3 (Fig. 3, A and B, and fig. S6C). These results indicate that the suppressive activity of high phyB levels overrides the antagonistic promotive activity of PIF3 on hypocotyl growth (17). This effect could result from phyB activity independent of PIF3, reduced intrinsic activity of PIF3, or phyB-induced dissociation of PIF3 from its DNA binding sites.

COP1-assembled E3 ligases were reported to be an important negative regulator of phyB levels (20). However, in agreement with other data (14, 16) we observed that PIF3 levels are reduced in dark-grown seedlings of both the cop1 and spa123 mutants, and no accumulation is observed in the light (Fig. 3E). These data suggest that the reduction in light-induced phyB degradation in the cop1 mutant partially is due to an indirect effect of the reduced levels of PIF3 (and possibly other PIFs) initially present in the dark. Regardless, the absence of detectable light-induced phyB degradation in the lrb123 mutant (Fig. 3C) indicates that COP1 is not sufficient for phyB degradation in the absence of the LRBs. Consistent with previous data that LRB1 and LRB2 are not directly involved in phyA degradation (23), we found that LRB3 also has no detectable role (fig. S7).

Regulated protein degradation through the 26S proteasome requires E3 ligase-mediated polyubiquitination of target proteins (21, 22). In support of the LRBs being components of an E3 ligase responsible for PIF3 polyubiqutination, light-induced ubiquitination of PIF3:GFP (fig. S8) is reduced in the lrb123 mutant (Fig. 4A). Moreover, photoactivated phyB, which coimmunoprecipitates with PIF3:GFP from extracts of light-treated seedlings, also displays high–molecular weight–shifted bands in wild-type but not in lrb123 mutant seedlings (Fig. 4B), which is suggestive of a subfraction of light-dependent, LRB-generated polyubiquitinated phyB molecules. More definitively, precipitation of total ubiquitinated proteins from the seedling extracts—followed by immunoblot detection of either phyB, PIF3:GFP, or endogenous PIF3—indicates that both phyB and PIF3 are polyubiquitinated in the wild-type in the light and that this concomitantly induced, bimolecular ubiquitination is undetectable (Fig. 4C) or markedly reduced (fig. S9) in the lrb123 mutant.

Fig. 4 LRB E3 ligases function in polyubiquitination of both PIF3 and phyB.

(A) Light-induced polyubiquitination of PIF3 is reduced in the lrb123 mutant. Dark-grown wild-type (col) or lrb123-mutant seedlings, transgenically, or not, expressing PIF3:GFP (PIF3:GFP/col and PIF3:GFP/lrb123, respectively) were irradiated with 10 min of red light (R), or not (Dk), before protein extraction and immunoprecipitation (IP) with antibody to GFP. The IP products were then analyzed by means of Western blot with antibody to GFP (left) or to ubiquitin (right). (B) Light-induced mobility shift of PIF3-bound phyB (phyB-ubi) is absent in the lrb123 mutant. Co-IP products prepared as in (A) were analyzed with antibody to phyB. (C) Light-induced polyubiquitination of both phyB and PIF3 is strongly reduced in the lrb123 mutant. Seedling growth and extraction was as in (A). Total ubiquitinated proteins were immunoprecipitated with TUBEs (tandem ubiquitin binding entities), then analyzed by means of Western blot with antibody to ubiquitin (left), to phyB (middle), or to GFP (right). (D) A Cullin3-LRB2 E3 ubiquitin-ligase complex ubiquitinates phosphomimic PIF3 (D6) in vitro. A Cullin3 E3 ubiquitin ligase complex was assembled with recombinant LRB2 protein and incubated with D6 or A20 PIF3:MYC (D6 is provided in fig. S4A) (8) variants in vitro (supplementary materials, materials and methods) before Western blot analysis with antibody to MYC.

Last, to examine whether LRB2 has the capacity to directly catalyze ubiquitination of PIF3, we assembled a Cullin3-based E3 ligase complex in vitro using recombinant LRB2 and human Cullin3/RBX1 and performed an in vitro ubiquitination assay. The data show that this complex can indeed ubiquitinate PIF3 in a phosphomimic-dependent manner, which is consistent with its PIF3 recognition mechanism and confirms its biochemical function (Fig. 4D and fig. S10). Although the evidence for LRB-dependent, light-induced ubiquitination of phyB in vivo is compelling (Fig. 4C), for undetermined reasons we were unable to detect such activity using the above in vitro assay.

We propose a mechanistic model (fig. S11), in which light-activated phyB induces multisite phosphorylation of PIF3 upon direct binding, enhancing the affinity of PIF3 for the LRBs, which then bind to Cul3, forming an active E3 ligase complex, which ubiquitinates both PIF3 and phyB, targeting them for degradation by the 26S proteasome. This mechanism of attenuation thus embodies a mutually assured destruction configuration of bidirectional signaling, directly at the receptor–primary-signaling-partner interface, that is unusual among reported mechanisms (13). Indicative of additional complexity, however, whereas light-induced phyB ubiquitination and degradation is essentially eliminated in the lrb123 mutant, light-induced PIF3 ubiquitination and degradation is slowed but not eliminated (Figs. 3 and 4 and fig. S6, C and D). This observation suggests the existence of partial functional redundancy between the LRBs and yet another unknown E3 ligase (or ligases) for PIF3 degradation and uncovers a dichotomy between PIF3 and phyB regulation.

Supplementary Materials

www.sciencemag.org/content/344/6188/1160/suppl/DC1

Materials and Methods

Figs. S1 to S11

Tables S1 and S2

References (26, 27)

References and Notes

  1. Acknowledgments: We thank R. J. Chalkley, A. Pfeiffer, M. Zhuang, and B. A. Schulman for materials and technical assistance and S. McCormick for comments on the manuscript. We also thank the Salk Institute and Arabidopsis Biological Resource Center for the Arabidopsis T-DNA insertion lines. The plasmid pGEX-CUL3 (split ’n’ coexpress)–Rbx1 used in the in vitro ubiquitination assays was provided by B. A. Schulman under a materials transfer agreement with St. Jude Children’s Research Hospital. For access to this reagent, contact B. A. Schulman. The supplementary materials contain additional data. This work was supported by the National Institutes of Health (NIH) (2R01 GM-047475), the U.S. Department of Energy (DOE) (DEFG03-87ER13742), and USDA ARS Current Research Information System (5335-21000-032-00D) to P.H.Q; by NIH (5R01GM066258) and DOE (DEFG02-08ER15973) to Z.Y.W.; by NIH (8P41GM103481) to A.L.B; and by NIH (P50 GM082250) to J.D.G.
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