Ligand-dependent protein interactions of the juvenile hormone receptor captured in real time
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
36609881
DOI
10.1111/febs.16719
Knihovny.cz E-zdroje
- Klíčová slova
- Hsp90, bHLH-PAS domain, dimerisation, hormone receptor, juvenile hormone,
- MeSH
- juvenilní hormony * metabolismus MeSH
- ligandy MeSH
- methopren * farmakologie metabolismus MeSH
- molekulární chaperony metabolismus MeSH
- regulace genové exprese MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- juvenilní hormony * MeSH
- ligandy MeSH
- methopren * MeSH
- molekulární chaperony MeSH
Juvenile hormone (JH) signalling provides vital regulatory functions during insect development via transcriptional regulation of genes critical for the progression of metamorphosis and oogenesis. Despite the importance of JH signalling, the underlying molecular mechanisms remain largely unknown. Our current understanding of the pathway depends on static end-point information and suffers from the lack of time-resolved data. Here, we have addressed the dynamic aspect of JH signalling by monitoring in real time the interactions of insect JH receptor proteins. Use of two tags that reconstitute a functional luciferase when in proximity enabled us to follow the rapid assembly of a JH receptor heterodimer from basic helix-loop-helix/Per-Arnt-SIM (bHLH-PAS) proteins, methoprene-tolerant (Met) and taiman (Tai), upon specific JH binding to Met. On a similar timescale (minutes), the dissociation of Met-Met complexes occurred, again strictly dependent on Met interaction with specific agonist ligands. To resolve questions regarding the regulatory role of the chaperone Hsp90/83 in the JHR complex formation, we used the same technique to demonstrate that the Met-Hsp83 complex persisted in the agonist absence but readily dissociated upon specific binding of JH to Met. Preincubation with the Hsp90 inhibitor geldanamycin showed that the chaperone interaction protected Met from degradation and was critical for Met to produce the active signalling dimer with Tai. Thus, the JH receptor functions appear to be governed by principles similar to those regulating the aryl hydrocarbon receptor, the closest vertebrate homologue of the arthropod JH receptor.
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Truman JW (2019) The evolution of insect metamorphosis. Curr Biol 29, R1252-R1268.
Bellés X (2020) Insect Metamorphosis: From Natural History to Regulation of Development and Evolution. Elsevier Inc., London.
Martin D, Chafino S & Franch-Marro X (2021) How stage identity is established in insects: the role of the metamorphic gene network. Curr Opin Insect Sci 43, 29-38.
Roy S, Saha TT, Zou Z & Raikhel AS (2018) Regulatory pathways controlling female insect reproduction. Annu Rev Entomol 63, 489-511.
Jindra M, Palli SR & Riddiford LM (2013) The juvenile hormone signaling pathway in insect development. Annu Rev Entomol 58, 181-204.
Santos CG, Humann FC & Hartfelder K (2019) Juvenile hormone signaling in insect oogenesis. Curr Opin Insect Sci 31, 43-48.
Miura T (2019) Juvenile hormone as a physiological regulator mediating phenotypic plasticity in pancrustaceans. Dev Growth Differ 61, 85-96.
Nunes C, Sucena E & Koyama T (2021) Endocrine regulation of immunity in insects. FEBS J 288, 3928-3947.
Goodman WG & Cusson M (2012) The juvenile hormones. In Insect Endocrinology (Gilbert LI, ed.), pp. 310-365. Elsevier, Amsterdam.
Tsang SSK, Law STS, Li C, Qu Z, Bendena WG, Tobe SS & Hui JHL (2020) Diversity of insect sesquiterpenoid regulation. Front Genet 11, 1027.
Ashok M, Turner C & Wilson TG (1998) Insect juvenile hormone resistance gene homology with the bHLH-PAS family of transcriptional regulators. Proc Natl Acad Sci USA 95, 2761-2766.
Charles J-P, Iwema T, Epa VC, Takaki K, Rynes J & Jindra M (2011) Ligand-binding properties of a juvenile hormone receptor, Methoprene-tolerant. Proc Natl Acad Sci USA 108, 21128-21133.
Miura K, Oda M, Makita S & Chinzei Y (2005) Characterization of the Drosophila Methoprene -tolerant gene product. FEBS J 272, 1169-1178.
Jindra M, Uhlirova M, Charles J-P, Smykal V & Hill RJ (2015) Genetic evidence for function of the bHLH-PAS protein Gce/Met as a juvenile hormone receptor. PLoS Genet 11, e1005394.
Li M, Liu P, Wiley JD, Ojani R, Bevan DR, Li J & Zhu J (2014) A steroid receptor coactivator acts as the DNA-binding partner of the methoprene-tolerant protein in regulating juvenile hormone response genes. Mol Cell Endocrinol 394, 47-58.
Milacek M, Bittova L, Tumova S, Luksan O, Hanus R, Kyjakova P, Machara A, Marek A & Jindra M (2021) Binding of de novo synthesized radiolabeled juvenile hormone (JH III) by JH receptors from the Cuban subterranean termite Prorhinotermes simplex and the German cockroach Blattella germanica. Insect Biochem Mol Biol 139, 103671.
Jindra M, Tumova S, Milacek M & Bittova L (2021) A decade with the juvenile hormone receptor. Adv Insect Physiol 60, 37-85.
Godlewski J, Wang S & Wilson TG (2006) Interaction of bHLH-PAS proteins involved in juvenile hormone reception in Drosophila. Biochem Biophys Res Commun 342, 1305-1311.
Li M, Mead EA & Zhu J (2011) Heterodimer of two bHLH-PAS proteins mediates juvenile hormone-induced gene expression. Proc Natl Acad Sci USA 108, 638-643.
Zhang Z, Xu J, Sheng Z, Sui Y & Palli SR (2011) Steroid receptor co-activator is required for juvenile hormone signal transduction through a bHLH-PAS transcription factor, methoprene tolerant. J Biol Chem 286, 8437-8447.
Kayukawa T, Minakuchi C, Namiki T, Togawa T, Yoshiyama M, Kamimura M, Mita K, Imanishi S, Kiuchi M, Ishikawa Y et al. (2012) Transcriptional regulation of juvenile hormone-mediated induction of Krüppel homolog 1, a repressor of insect metamorphosis. Proc Natl Acad Sci USA 109, 11729-11734.
Bai J, Uehara Y & Montell DJ (2000) Regulation of invasive cell behavior by taiman, a Drosophila protein related to AIB1, a steroid receptor coactivator amplified in breast cancer. Cell 103, 1047-1058.
Jindra M, McKinstry WJ, Nebl T, Bittova L, Ren B, Shaw J, Phan T, Lu L, Low JKK, Mackay JP et al. (2021) Purification of an insect juvenile hormone receptor complex enables insights into its post-translational phosphorylation. J Biol Chem 297, 101387.
Zou Z, Saha TT, Roy S, Shin SW, Backman TWH, Girke T, White KP & Raikhel AS (2013) Juvenile hormone and its receptor, methoprene-tolerant, control the dynamics of mosquito gene expression. Proc Natl Acad Sci USA 110, E2173-E2181.
Pongratz I, Mason GG & Poellinger L (1992) Dual roles of the 90-kDa heat shock protein hsp90 in modulating functional activities of the dioxin receptor. J Biol Chem 267, 13728-13734.
Whitelaw ML, McGuire J, Picard D, Gustafsson JA & Poellinger L (1995) Heat shock protein hsp90 regulates dioxin receptor function in vivo. Proc Natl Acad Sci USA 92, 4437-4441.
He Q, Wen D, Jia Q, Cui C, Wang J, Palli SR & Li S (2014) Heat shock protein 83 (Hsp83) facilitates Methoprene-tolerant (Met) nuclear import to modulate juvenile hormone signaling. J Biol Chem 289, 27874-27885.
Kazlauskas A, Sundström S, Poellinger L & Pongratz I (2001) The hsp90 chaperone complex regulates intracellular localization of the dioxin receptor. Mol Cell Biol 21, 2594-2607.
Soshilov A & Denison MS (2011) Ligand displaces heat shock protein 90 from overlapping binding sites within the aryl hydrocarbon receptor ligand-binding domain. J Biol Chem 286, 35275-35282.
Soshilov AA, Motta S, Bonati L & Denison MS (2020) Transitional states in ligand-dependent transformation of the aryl hydrocarbon receptor into its DNA-binding form. Int J Mol Sci 21, 2474.
Dixon AS, Schwinn MK, Hall MP, Zimmerman K, Otto P, Lubben TH, Butler BL, Binkowski BF, Machleidt T, Kirkland TA et al. (2016) NanoLuc complementation reporter optimized for accurate measurement of protein interactions in cells. ACS Chem Biol 11, 400-408.
Masterson M, Bittar R, Chu H, Yamanaka N & Haga-Yamanaka S (2022) Rapid assessment of insect steroid hormone entry into cultured cells. Front Physiol 12, 816058.
Bittova L, Jedlicka P, Dracinsky M, Kirubakaran P, Vondrasek J, Hanus R & Jindra M (2019) Exquisite ligand stereoselectivity of a Drosophila juvenile hormone receptor contrasts with its broad agonist repertoire. J Biol Chem 294, 410-423.
Kayukawa T & Shinoda T (2015) Functional characterization of two paralogous JH receptors, methoprene-tolerant 1 and 2, in the silkworm, Bombyx mori (Lepidoptera: Bombycidae). Appl Entomol Zool 50, 383-391.
Miyakawa H & Iguchi T (2017) Comparative luciferase assay for establishing reliable in vitro screening system of juvenile hormone agonists. J Appl Toxicol 37, 1082-1090.
Chen HS, Singh SS & Perdew GH (1997) The Ah receptor is a sensitive target of geldanamycin-induced protein turnover. Arch Biochem Biophys 348, 190-198.
Kakaley EK, Wang HY & LeBlanc GA (2017) Agonist-mediated assembly of the crustacean methyl farnesoate receptor. Sci Rep 7, 45071.
Kakaley EK, Eytcheson SA & LeBlanc GA (2017) Ligand-mediated receptor assembly as an end point for high-throughput chemical toxicity screening. Environ Sci Technol 51, 9327-9333.
Yao TP, Forman BM, Jiang Z, Cherbas L, Chen JD, McKeown M, Cherbas P, Cherbas P & Evans RM (1993) Functional ecdysone receptor is the product of EcR and ultraspiracle genes. Nature 366, 476-479.
Trenker R & Jura N (2020) Receptor tyrosine kinase activation: from the ligand perspective. Curr Opin Cell Biol 63, 174-185.
Hilger D (2021) The role of structural dynamics in GPCR-mediated signaling. FEBS J 288, 2461-2489.
Denison MS, Soshilov AA, He G, DeGroot DE & Zhao B (2011) Exactly the same but different: promiscuity and diversity in the molecular mechanisms of action of the aryl hydrocarbon (dioxin) receptor. Toxicol Sci 124, 1-22.
Henry EC & Gasiewicz TA (1993) Transformation of the aryl hydrocarbon receptor to a DNA-binding form is accompanied by release of the 90 kDa heat-shock protein and increased affinity for 2,3,7,8-tetrachlorodibenzo-p-dioxin. Biochem J 294, 95-101.
Gradin K, McGuire J, Wenger RH, Kvietikova I, Whitelaw ML, Toftgard R, Tora L, Gassmann M & Poellinger L (1996) Functional interference between hypoxia and dioxin signal transduction pathways: competition for recruitment of the Arnt transcription factor. Mol Cell Biol 16, 5221-5231.
Bell DR & Poland A (2000) Binding of aryl hydrocarbon receptor (AhR) to AhR-interacting protein. The role of hsp90. J Biol Chem 275, 36407-36414.
Isaacs JS, Jung YJ, Mimnaugh EG, Martinez A, Cuttitta F & Neckers LM (2002) Hsp90 regulates a von Hippel Lindau-independent hypoxia-inducible factor-1 alpha-degradative pathway. J Biol Chem 277, 29936-29944.
Isaacs JS, Jung YJ & Neckers L (2004) Aryl hydrocarbon nuclear translocator (ARNT) promotes oxygen-independent stabilization of hypoxia-inducible factor-1alpha by modulating an Hsp90-dependent regulatory pathway. J Biol Chem 279, 16128-16135.
He Q, Zhang Y, Zhang X, Xu D, Dong W, Li S & Wu R (2017) Nucleoporin Nup358 facilitates nuclear import of Methoprene-tolerant (Met) in an importin β- and Hsp83-dependent manner. Insect Biochem Mol Biol 81, 10-18.
Taipale M, Krykbaeva I, Koeva M, Kayatekin C, Westover KD, Karras GI & Lindquist S (2012) Quantitative analysis of HSP90-client interactions reveals principles of substrate recognition. Cell 150, 987-1001.
Sahasrabudhe P, Rohrberg J, Biebl MM, Rutz DA & Buchner J (2017) The plasticity of the Hsp90 Co-chaperone system. Mol Cell 67, 947-961.
Radli M & Rudiger SGD (2018) Dancing with the diva: Hsp90-client interactions. J Mol Biol 430, 3029-3040.
Prodromou C & Bjorklund DM (2022) Advances towards understanding the mechanism of action of the Hsp90 complex. Biomolecules 12, 600.
Kirschke E, Goswami D, Southworth D, Griffin PR & Agard DA (2014) Glucocorticoid receptor function regulated by coordinated action of the Hsp90 and Hsp70 chaperone cycles. Cell 157, 1685-1697.
Verba KA, Wang RY, Arakawa A, Liu Y, Shirouzu M, Yokoyama S & Agard DA (2016) Atomic structure of Hsp90-Cdc37-Cdk4 reveals that Hsp90 traps and stabilizes an unfolded kinase. Science 352, 1542-1547.
Wang RY, Noddings CM, Kirschke E, Myasnikov AG, Johnson JL & Agard DA (2022) Structure of Hsp90-Hsp70-hop-GR reveals the Hsp90 client-loading mechanism. Nature 601, 460-464.
Lindebro MC, Poellinger L & Whitelaw ML (1995) Protein-protein interaction via PAS domains: role of the PAS domain in positive and negative regulation of the bHLH/PAS dioxin receptor-Arnt transcription factor complex. EMBO J 14, 3528-3539.
Perdew GH & Bradfield CA (1996) Mapping the 90 kDa heat shock protein binding region of the Ah receptor. Biochem Mol Biol Int 39, 589-593.
Powell E, Wang Y, Shapiro DJ & Xu W (2010) Differential requirements of Hsp90 and DNA for the formation of estrogen receptor homodimers and heterodimers. J Biol Chem 285, 16125-16134.
Greb-Markiewicz B, Orłowski M, Dobrucki J & Ożyhar A (2011) Sequences that direct subcellular traffic of the Drosophila methoprene-tolerant protein (MET) are located predominantly in the PAS domains. Mol Cell Endocrinol 345, 16-26.
Greb-Markiewicz B, Sadowska D, Surgut N, Godlewski J, Zarębski M & Ożyhar A (2015) Mapping of the sequences directing localization of the Drosophila germ cell-expressed protein (GCE). PLoS One 10, e0133307.
Silver K, Jiang H, Fu J, Phillips TW, Beeman RW & Park Y (2014) The Tribolium castaneum cell line TcA: a new tool kit for cell biology. Sci Rep 4, 6840.
MET goes to the membrane-A new place for the "old" juvenile hormone receptor