The Lnk/SH2B adaptor provides a fail-safe mechanism to establish the Insulin receptor-Chico interaction
Cell Communication and Signaling volume 11, Article number: 26 (2013)
Insulin/insulin-like growth factor signalling (IIS) has been described as one of the major pathways involved in growth control and homeostasis in multicellular organisms. Whereas its core components are well established, less is known about the molecular functions of IIS regulators. The adaptor molecule Lnk/SH2B has been implicated in IIS but the mechanism by which it promotes IIS activity has remained enigmatic.
In this study, we analyse genetic and physical interactions among InR, Chico and Lnk in Drosophila tissues. FRET analysis reveals in vivo binding between all three molecules. Genetically, Lnk acts upstream of Chico. We demonstrate that Chico’s plasma membrane localisation is ensured by both its PH domain and by the interaction with Lnk. Furthermore, Lnk is able to recruit an intracellular InR fragment to the membrane.
Thus, by acting as a scaffolding molecule that ensures InR and Chico enrichment at the membrane, Lnk provides a fail-safe mechanism for IIS activation.
The Insulin/insulin-like growth factor signalling (IIS) pathway has emerged in the last decade as one of the major signalling pathways involved in the control of growth, body size and homeostasis in multicellular organisms[1–4].
The main intracellular components of IIS in Drosophila are Chico, the homologue of the Insulin Receptor Substrates (IRS), the lipid kinase phosphoinositide 3-kinase (PI3K), the lipid phosphatase PTEN and the serine-threonine kinase dAkt/PKB[5–10]. These intracellular signalling components need to be recruited to the cortical membrane to regulate signalling activity[5, 7, 11–13]. In addition to the core components, regulators such as Susi, Steppke and Lnk[16, 17] modulate IIS activity.
The Lnk adaptor protein has been identified in an unbiased screen as a component of the pathway based on the reduced body size and lipid accumulation observed in lnk mutant flies. Mutations in the lnk locus were able to rescue the overgrowth phenotype caused by overexpression of InR, but not to suppress the overgrowth promoted by high activity of PI3K, suggesting that Lnk acts between InR and PI3K in the IIS pathway. Moreover, phosphorylation of PKB and tGPH reporter localisation, both readouts of IIS pathway activity, were impaired in lnk mutants. Lnk is the unique Drosophila member of the SH2B protein family. This protein family is characterised by several conserved domains: the N-terminal proline-rich stretch, a pleckstrin homology (PH) domain, a Src homology 2 (SH2) domain, and a C-terminal c-Cbl recognition motif[19–21]. Alleles with inactive PH or SH2 domains have similar phenotypes to those carrying premature stop codons, suggesting that both domains are essential for Lnk activity.
Here we study the molecular function of Lnk in Drosophila. We first apply the Förster Resonance Energy Transfer (FRET) technique in Drosophila larvae to demonstrate that Lnk binds to Chico and InR in vivo. Second, we show that Lnk functions upstream of Chico. Finally, we demonstrate that Lnk ensures proper localisation of InR and Chico to trigger IIS.
Results and discussion
InR, Chico and Lnk physically interact in vivo
Previous studies have demonstrated that a mammalian homologue of Lnk, SH2B, co-immunoprecipitates with the mammalian InR in cultured cells[20, 22]. Moreover, Lnk and Chico have been shown to co-immunoprecipitate in Drosophila S2 cells. However, the interactions between the three molecules in vivo have remained elusive. Therefore, we set out to investigate the binding between InR, Chico and Lnk using FRET in Drosophila tissues. We generated constructs to drive expression of tagged InR, Chico and Lnk proteins based on the UAS/Gal4 system. In order to analyse the physical interactions between the three molecules in vivo, we modified phiC31 UASattB vectors to C-terminally tag the expressed proteins with Cyan Fluorescent Protein (CFP) and monomeric Red Fluorescent Protein (RFP), respectively (see Methods).
We first assessed the FRET efficiency (FRETeff) between the known binding partners InR and Chico by overexpressing UAS-InR-CFP and UAS-chico-RFP with hsp-Gal4 in larval salivary glands. We chose the salivary glands because of the large cell size. FRET between CFP and RFP (FRETeff = 14.1 ± 3%) was observed in 71% of the tissue samples examined after insulin stimulation (Figure 1A and F). Interestingly, we detected FRET between the two molecules only in 20% of the samples in the absence of insulin (FRETeff = 13.5 ± 1%), indicating that InR-Chico binding is stimulated by insulin as previously reported[24, 25].
We next investigated the binding of Lnk to Chico. In lnk-CFP/chico-RFP salivary glands, FRETeff was 14.8 ± 4% in 73% of the samples upon insulin stimulation (Figure 1B and F). By contrast, non-stimulated tissue samples showed a reduction in Lnk-Chico interaction (FRETeff = 13.3 ± 3% in 30% of samples), suggesting that, like Chico-InR binding, the Chico-Lnk interaction depends on insulin stimulation.
We also tested whether Lnk can directly bind to InR and found positive energy transfer in 53% of the salivary glands examined (FRETeff = 14 ± 3%; Figure 1C and F). Remarkably, when we analysed FRET between Lnk and InR in the absence of insulin, FRETeff = 10.8 ± 2% was observed in 60% of the samples, implying that the interaction between Lnk and InR occurs, at least partially, in an insulin-independent way. We did not detect energy transfer between Delta-RFP (Dl-RFP)[26, 27] and InR-CFP (Figure 1D and F, FRETeff < 3%) or Lnk-CFP (Figure 1E and F, FRETeff < 3%), excluding that InR-CFP and Lnk-CFP unspecifically interact with membrane-bound proteins. Thus, Lnk acts as a direct binding partner of both InR and Chico in Drosophila tissues. Interestingly, the Chico-Lnk and Chico-InR interactions are insulin dependent, whereas Lnk and InR are capable of interacting without insulin stimulation. These differences in response to insulin may reflect specific functions of the molecules under examination.
Lnk facilitates the recruitment of Chico to the membrane
Once we established that Lnk is forming a complex with InR and Chico, we wondered about the molecular function of Lnk. To address whether Lnk is acting in parallel to Chico, we first investigated whether overexpression of lnk was able to rescue the decrease of IIS activity in chico mutant cells. The MARCM (mosaic analysis with a repressible cell marker) system was used to generate clonal populations of chico mutant cells that overexpress lnk-CFP and are marked by the expression of GFP. We induced MARCM clones in eye imaginal discs and performed immunostainings against phospho-PKB to assess IIS activity. Whereas overexpression of lnk-CFP was able to increase phospho-PKB levels in clones (marked by GFP) in comparison to wild-type tissue (Figure 2A and C), we did not observe a rescue of the low phospho-PKB levels in chico−/− clones upon lnk-CFP overexpression (Figure 2B and D).
For the inverse experiment, we used lnk mutant salivary glands and analysed IIS pathway activity by means of a tGPH reporter. In lnk mutant salivary glands, we observed the tGPH reporter mainly in the cytoplasm, which indicates low IIS activity (Figure 2F,). By contrast, overexpression of chico-RFP in lnk mutant salivary glands resulted in localisation of the tGPH reporter to the plasma membrane, reflecting high IIS activity (Figure 2E and G). Thus, overexpression of chico-RFP counteracts the loss of lnk function, suggesting that Chico acts downstream of Lnk.
To analyse whether Lnk facilitates the localisation of Chico, we first studied the localisation of Chico-RFP in lnk mutant salivary glands. We determined the intensity of the Chico-RFP signal at the membrane and in the cytoplasm to assess the relative amounts of protein in these compartments under different experimental conditions (see Methods). The membrane localisation of Chico-RFP was only slightly reduced in lnk mutant tissue in comparison to wild-type tissue (Figure 2H, I and Additional file1: Figure S1A), probably due to the PH domain of Chico. In fact, when we expressed a PH-domain mutated form of Chico (Chico-PH*-RFP) in a lnk mutant background, we noticed a relocalisation of Chico-PH*-RFP from the membrane to the cytoplasm (Figure 2K and Additional file1: Figure S1A). By contrast, Chico-PH*-RFP showed significant localisation to the plasma membrane in wild-type tissue (Figure 2J and Additional file1: Figure S1A), indicating that Lnk is sufficient to substitute the function of the PH domain in Chico-PH*-RFP. Thus, Lnk provides a redundant means to properly localise Chico at the cortical membrane.
Lnk ensures InR enrichment at the cortical membrane
Our genetic and localisation data of Chico and Lnk might seem contradictory to previous genetic interaction experiments between chico and lnk mutants; if Lnk was only required for proper Chico function, chico; lnk double mutants should display similar phenotypes to chico single mutants. However, whereas the single mutants are reduced in size but viable, the chico; lnk double mutants turned out to be lethal. One way to reconcile these findings is to propose an additional direct function of Lnk on InR.
We analysed InR-CFP localisation in lnk mutant salivary glands to test whether Lnk facilitates InR localisation. In contrast to InR-CFP in wild-type tissue, where InR-CFP was located mainly at the cortical membrane (Figure 3A and Additional file1: Figure S1B), InR-CFP was decreased at the membrane in a lnk mutant background (Figure 3B and Additional file1: Figure S1B). However, a fraction of InR-CFP still localised at the plasma membrane, most likely due to InR’s transmembrane domain. We next generated an intracellular InR construct (hereafter InRINTRA) containing the intracellular domain of InR (beginning with the kinase domain) fused to CFP at the C-terminus (InRINTRA-CFP). InRINTRA-CFP membrane localisation was reduced already in a wild-type background (Figure 3C and Additional file1: Figure S1B), whereas full-length InR-CFP showed a similar effect only in lnk mutant salivary glands. In a lnk mutant background, cortical accumulation of InRINTRA-CFP was reduced more strongly (Figure 3D and Additional file1: Figure S1B), further supporting the role of Lnk in locking InR to the membrane. Moreover, overexpression of InRINTRA-CFP together with lnk-RFP restored cortical localisation of InRINTRA-CFP, showing both molecules at the plasma membrane (Figure 3E and Additional file1: Figure S1B). The membrane localisation was essentially abolished when a PH domain mutant version of Lnk was expressed (Figure 3F and Additional file1: Figure S1B). These experiments strongly suggest that Lnk contributes to the cortical localisation of InR by interacting with the intracellular part of InR.
Finally, we investigated the interaction between InR-CFP and Chico-RFP in a lnk mutant background. Similarly to Lnk, Chico-RFP was able to recruit InRINTRA-CFP to the membrane, either in a wild-type (Figure 4A and Additional file1: Figure S1C) or in a lnk mutant (Figure 4B and Additional file1: Figure S1C) background, although a significant proportion of InRINTRA-CFP and Chico-RFP remained in the cytoplasm when Lnk was lacking. However, when InRINTRA-CFP and Chico-PH*-RFP were overexpressed in lnk mutant salivary glands, the membrane enrichment of both was abolished (Figure 4D and Additional file1: Figure S1C) in contrast to the situation where Lnk was present (Figure 4C and Additional file1: Figure S1C). Thus, Lnk is required to reinforce the InR-Chico interaction at the membrane.
By combining genetics with in vivo localisation studies on InR and its two adaptor molecules, Chico and Lnk, we gained insight into the molecular mechanisms at the plasma membrane that ensure proper IIS activation. Our data support the following model: Lnk is required to enrich InR and Chico at the plasma membrane (Figure 4). In a lnk mutant situation, fractions of InR and Chico are still localised at the cortical membrane, due to their transmembrane and PH domains, respectively. Thus, the IIS pathway is partially active in the absence of Lnk (Figure 4E”). In chico mutants, InR is capable of directly interacting with PI3K; hence chico mutants are viable (Figure 4E’). By contrast, chico; lnk double mutants are lethal, probably due to mislocalisation and/or instability of InR, resulting in an insufficient signal from the receptor to PI3K (Figure 4E”’). Mutations in lnk weaken the InR-Chico interaction, reducing the capability of InR to phosphorylate Chico, as it was observed by Song and colleagues. Future studies should aim at elucidating the precise mechanism of how Lnk promotes the InR-Chico interaction. It remains to be determined whether Lnk is required for trafficking, localisation at specific subdomains of the cortical membrane or stabilisation of InR and/or Chico.
Lnk, chico and InR constructs
PCRs from Drosophila lnk, chico and InR genes were performed using primers listed in Additional file2: Table S1. Point mutations introduced in the PH domains of Lnk and Chico were C254Y and W100L, respectively[17, 29]. PCR products were cloned into pENTR-TOPO (Invitrogen). Subsequent Gateway reactions were performed to shuffle the sequences into modified pUASTattbCFP and pUASTattbRFP vectors.
The pUASTattb vector was modified in order to introduce CFP or RFP coding sequences. pUASTattb and pAWC or pAWR (obtained from Drosophila Genomics Resource Center) were digested with NheI and NotI to swap the Gateway cassette from the pUASattb plasmid to pAWC or pAWR cassettes, respectively, to introduce CFP or mRFP coding sequences downstream of the attR2 sites.
Fly transgenes and mutants
Mutant alleles used were lnk4Q3 and chico1. hsp-Gal4 and GMR-Gal4 were used to drive expression of the transgenes. Vectors carrying UAS-InR, InRINTRA, chico or lnk were injected in ZH-attP-86Fb or ZH-attP-44F (InRINTRA) embryos. The functionality of the tagged proteins was confirmed as follows (Additional file3: Figure S2): Overexpression of UAS-InR-CFP using the GMR-Gal4 driver resulted in a significant overgrowth of the eyes as compared to GMR-Gal4 UAS-GFP control flies. Overexpression of UAS-chico-RFP and UAS-lnk-CFP (by means of MARCM clones) in eye imaginal discs promoted higher phospho-PKB levels (as a readout for IIS activity). The tGPH line was used as a reporter for IIS activity. UAS-Delta-RFP (Bloomington 26696) was used to perform the negative controls for the FRET experiments.
Sample processing, FRET analyses and quantification of sublocalisation
Transgenic lines were crossed to hsp-Gal4. Third instar larvae were incubated at 37°C for 1 h. After 45 min of recovery, salivary glands were dissected in PBS and incubated for 15 min in Schneider’s medium with or without insulin (100 nM). After insulin treatment, salivary glands were fixed in 4% paraformaldehyde.
To examine interactions between Lnk, Chico and InR proteins, the FRET sensitised emission method was used. CFP was utilised as donor molecule and mRFP as acceptor molecule. FRET was analysed using a Leica SP2-AOBS confocal microscope. The FRET values were corrected for background fluorescence and crossover of donor and acceptor fluorescence. Corrected FRET was calculated as FRETc = FRET - (a x CFP) - (b x RFP)/RFP, with a and b representing the fractions of bleed-through of CFP and RFP fluorescence, respectively, through the FRET filter channel. These values are presented as FRET efficiency (FRETeff). FRETeff values were averaged from regions of interest (ROIs) observed in cells from three independent experiments (n > 10) per condition and represented as mean ± standard deviation. For our sensors, we considered FRETeff ≥10% as positive FRET[33–35]. However, it is generally accepted that absence of FRET yields values <3%. To determine the percentage of samples (tissues) with positive FRET, we considered any ROI with FRETeff ≥10% after scanning regions where the two constructs co-localised as positive. After applying Gaussian Blur filter (Sigma: 2) with ImageJ software, FRETc was presented in pseudocolour mode according to a temperature-based Look Up Table (LUT) with blue (cold) indicating low values and red (hot) indicating high values. LUT was linear, covering the full range of the data.
To quantify the subcellular distribution of the tagged proteins, the Plot Profile function from ImageJ software was used. Pixel intensities at the membrane and in the cytoplasm were measured across the cell (at least two cells were measured in each tissue sample), avoiding the nuclei and taking Actin pixel intensity as indicator for the membrane sub-compartment. Pixel intensities were averaged for each fraction, and the ratio between the means was calculated as a measure for the relative amount of protein per sub-compartment. The R package was used to perform one-tail t-test statistical analyses and boxplots.
Immunostainings and clonal analysis
For dominantly marked clones (MARCM system), FRT40 chico1 or FRT40iso and y w hs-flp UAS-GFP; tub-Gal80 FRT40/CyO y+; tub-Gal4/TM6B flies were used. Clones were induced in second instar larvae (48 h after egg deposition (AED)) at 37°C for 15 min (dissection 96 h AED).
Rabbit anti Drosophila phospho-Akt/PKB Ser505 (1:300, Cell Signaling) staining was carried out on eye imaginal discs. Discs were dissected in PBS and fixed in 4% paraformaldehyde for 20 min at room temperature. After blocking (PBS, 0.3% Triton X-100, 2% NDS), imaginal discs were incubated with primary antibody at 4°C overnight. Goat anti-rabbit-Cy3 (1:200, Molecular Probes) was used as secondary antibody for 2 h at room temperature. AlexaFluor 647 phalloidin (1:40, Molecular Probes) was used for Actin staining. Nuclei were stained with DAPI before mounting in Vectashield. Samples were captured using a Leica SPE TCS confocal laser scanning microscope. Images were processed using NIH ImageJ software. Final artwork was prepared using Adobe Photoshop CS5 and Illustrator.
Broughton S, Partridge L: Insulin/IGF-like signalling, the central nervous system and aging. Biochem J. 2009, 418 (1): 1-12. 10.1042/BJ20082102.
Garofalo RS: Genetic analysis of insulin signaling in Drosophila. Trends Endocrinol Metab. 2002, 13 (4): 156-162. 10.1016/S1043-2760(01)00548-3.
Oldham S, Bohni R, Stocker H, Brogiolo W, Hafen E: Genetic control of size in Drosophila. Philos Trans R Soc Lond B Biol Sci. 2000, 355 (1399): 945-952. 10.1098/rstb.2000.0630.
Teleman AA: Molecular mechanisms of metabolic regulation by insulin in Drosophila. Biochem J. 2010, 425 (1): 13-26. 10.1042/BJ20091181.
Weinkove D, Neufeld TP, Twardzik T, Waterfield MD, Leevers SJ: Regulation of imaginal disc cell size, cell number and organ size by Drosophila class I(A) phosphoinositide 3-kinase and its adaptor. Curr Biol. 1999, 9 (18): 1019-1029. 10.1016/S0960-9822(99)80450-3.
Verdu J, Buratovich MA, Wilder EL, Birnbaum MJ: Cell-autonomous regulation of cell and organ growth in Drosophila by Akt/PKB. Nat Cell Biol. 1999, 1 (8): 500-506. 10.1038/70293.
Stocker H, Andjelkovic M, Oldham S, Laffargue M, Wymann MP, Hemmings BA, Hafen E: Living with lethal PIP3 levels: viability of flies lacking PTEN restored by a PH domain mutation in Akt/PKB. Science. 2002, 295 (5562): 2088-2091. 10.1126/science.1068094.
Shepherd PR, Withers DJ, Siddle K: Phosphoinositide 3-kinase: the key switch mechanism in insulin signalling. Biochem J. 1998, 333 (Pt 3): 471-490.
Scanga SE, Ruel L, Binari RC, Snow B, Stambolic V, Bouchard D, Peters M, Calvieri B, Mak TW, Woodgett JR: The conserved PI3’K/PTEN/Akt signaling pathway regulates both cell size and survival in Drosophila. Oncogene. 2000, 19 (35): 3971-3977. 10.1038/sj.onc.1203739.
Goberdhan DC, Paricio N, Goodman EC, Mlodzik M, Wilson C: Drosophila tumor suppressor PTEN controls cell size and number by antagonizing the Chico/PI3-kinase signaling pathway. Genes Dev. 1999, 13 (24): 3244-3258. 10.1101/gad.13.24.3244.
Coffer PJ, Jin J, Woodgett JR: Protein kinase B (c-Akt): a multifunctional mediator of phosphatidylinositol 3-kinase activation. Biochem J. 1998, 335 (1): 1-13.
Downward J: Mechanisms and consequences of activation of protein kinase B/Akt. Curr Opin Cell Biol. 1998, 10 (2): 262-267. 10.1016/S0955-0674(98)80149-X.
Yenush L, Makati KJ, Smith-Hall J, Ishibashi O, Myers MG, White MF: The Pleckstrin Homology Domain Is the Principle Link between the Insulin Receptor and IRS-1. J Biol Chem. 1996, 271 (39): 24300-24306. 10.1074/jbc.271.39.24300.
Wittwer F, Jaquenoud M, Brogiolo W, Zarske M, Wustemann P, Fernandez R, Stocker H, Wymann MP, Hafen E: Susi, a negative regulator of Drosophila PI3-kinase. Dev Cell. 2005, 8 (6): 817-827. 10.1016/j.devcel.2005.04.002.
Fuss B, Becker T, Zinke I, Hoch M: The cytohesin Steppke is essential for insulin signalling in Drosophila. Nature. 2006, 444 (7121): 945-948. 10.1038/nature05412.
Song W, Ren D, Li W, Jiang L, Cho KW, Huang P, Fan C, Song Y, Liu Y, Rui L: SH2B regulation of growth, metabolism, and longevity in both insects and mammals. Cell Metab. 2010, 11 (5): 427-437. 10.1016/j.cmet.2010.04.002.
Werz C, Kohler K, Hafen E, Stocker H: The Drosophila SH2B family adaptor Lnk acts in parallel to chico in the insulin signaling pathway. PLoS Genet. 2009, 5 (8): e1000596-10.1371/journal.pgen.1000596.
Britton JS, Lockwood WK, Li L, Cohen SM, Edgar BA: Drosophila’s Insulin/PI3-kinase pathway coordinates cellular metabolism with nutritional conditions. Dev Cell. 2002, 2 (2): 239-249. 10.1016/S1534-5807(02)00117-X.
Yokouchi M, Suzuki R, Masuhara M, Komiya S, Inoue A, Yoshimura A: Cloning and characterization of APS, an adaptor molecule containing PH and SH2 domains that is tyrosine phosphorylated upon B-cell receptor stimulation. Oncogene. 1997, 15 (1): 7-15. 10.1038/sj.onc.1201163.
Riedel H, Wang J, Hansen H, Yousaf N: PSM, an insulin-dependent, pro-rich, PH, SH2 domain containing partner of the insulin receptor. J Biochem. 1997, 122 (6): 1105-1113. 10.1093/oxfordjournals.jbchem.a021868.
Huang X, Li Y, Tanaka K, Moore KG, Hayashi JI: Cloning and characterization of Lnk, a signal transduction protein that links T-cell receptor activation signal to phospholipase C gamma 1, Grb2, and phosphatidylinositol 3-kinase. Proc Natl Acad Sci USA. 1995, 92 (25): 11618-11622. 10.1073/pnas.92.25.11618.
Kotani K, Wilden P, Pillay TS: SH2-Balpha is an insulin-receptor adapter protein and substrate that interacts with the activation loop of the insulin-receptor kinase. Biochem J. 1998, 335 (Pt 1): 103-109.
Brand AH, Perrimon N: Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development. 1993, 118 (2): 401-415.
Glatter T, Schittenhelm RB, Rinner O, Roguska K, Wepf A, Junger MA, Kohler K, Jevtov I, Choi H, Schmidt A: Modularity and hormone sensitivity of the Drosophila melanogaster insulin receptor/target of rapamycin interaction proteome. Mol Syst Biol. 2011, 7: 547-
Pflieger D, Junger MA, Muller M, Rinner O, Lee H, Gehrig PM, Gstaiger M, Aebersold R: Quantitative proteomic analysis of protein complexes: concurrent identification of interactors and their state of phosphorylation. Mol Cell Proteomics. 2008, 7 (2): 326-346.
Fehon RG, Kooh PJ, Rebay I, Regan CL, Xu T, Muskavitch MAT, Artavanis-Tsakonas S: Molecular interactions between the protein products of the neurogenic loci Notch and Delta, two EGF-homologous genes in Drosophila. Cell. 1990, 61 (3): 523-534. 10.1016/0092-8674(90)90534-L.
Hagedorn EJ, Bayraktar JL, Kandachar VR, Bai T, Englert DM, Chang HC: Drosophila melanogaster auxilin regulates the internalization of Delta to control activity of the Notch signaling pathway. J Cell Biol. 2006, 173 (3): 443-452. 10.1083/jcb.200602054.
Yenush L, Fernandez R, Myers MG, Grammer TC, Sun XJ, Blenis J, Pierce JH, Schlessinger J, White MF: The Drosophila insulin receptor activates multiple signaling pathways but requires insulin receptor substrate proteins for DNA synthesis. Mol Cell Biol. 1996, 16 (5): 2509-2517.
Oldham S, Stocker H, Laffargue M, Wittwer F, Wymann M, Hafen E: The Drosophila insulin/IGF receptor controls growth and size by modulating PtdInsP(3) levels. Development. 2002, 129 (17): 4103-4109.
Hay BA, Wolff T, Rubin GM: Expression of baculovirus P35 prevents cell death in Drosophila. Development. 1994, 120 (8): 2121-2129.
Bischof J, Maeda RK, Hediger M, Karch F, Basler K: An optimized transgenesis system for Drosophila using germ-line-specific phiC31 integrases. Proc Natl Acad Sci USA. 2007, 104 (9): 3312-3317. 10.1073/pnas.0611511104.
Jiang X, Sorkin A: Coordinated traffic of Grb2 and Ras during epidermal growth factor receptor endocytosis visualized in living cells. Mol Biol Cell. 2002, 13 (5): 1522-1535. 10.1091/mbc.01-11-0552.
Galperin E, Verkhusha VV, Sorkin A: Three-chromophore FRET microscopy to analyze multiprotein interactions in living cells. Nat Methods. 2004, 1 (3): 209-217. 10.1038/nmeth720.
van der Krogt GN, Ogink J, Ponsioen B, Jalink K: A comparison of donor-acceptor pairs for genetically encoded FRET sensors: application to the Epac cAMP sensor as an example. PLoS One. 2008, 3 (4): e1916-10.1371/journal.pone.0001916.
Almudi I, Corominas M, Serras F: Competition between SOCS36E and Drk modulates Sevenless receptor tyrosine kinase activity. J Cell Sci. 2010, 123 (Pt 22): 3857-3862.
We thank Anni Straessle, Julia Lüdke and Igor Vuillez for technical support, the Bloomington stock center for flies, and the Light Microscopy Center at ETH Zürich for the use of the confocal facility.
The authors declare that they have no competing interests.
IA, EH and HS conceived the experiments. IA and IP performed the experiments. IA analysed the data. IA and HS wrote the paper. All the authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: Table S1: Primer sequences used to generate pENTR vectors for subsequent Gateway cloning. (XLSX 41 KB)
Additional file 3: Figure S2: InR-CFP, Chico-RFP and Lnk-CFP fusion proteins promote IIS activity. (A-C) Overexpression of UAS-InR-CFP using the GMR-Gal4 driver (B) results in overgrown eyes as compared to the control (UAS-GFP, A). (C) Eye areas of GMR > InR-CFP and GMR > GFP flies (n = 13, p < 0.01). (D-D””) MARCM clones in eye discs overexpressing UAS-Chico-RFP show an increase in phospho-PKB levels (D” and D””). (E-E””) MARCM clones overexpressing Lnk-CFP (E’) exhibit increased phospho-PKB levels (E” and E””). Scale bars represent 100 μm (A and B) and 50 μm (D and E), respectively. (JPEG 3 MB)
About this article
Cite this article
Almudi, I., Poernbacher, I., Hafen, E. et al. The Lnk/SH2B adaptor provides a fail-safe mechanism to establish the Insulin receptor-Chico interaction. Cell Commun Signal 11, 26 (2013). https://doi.org/10.1186/1478-811X-11-26