Abstract
Key message
We found two subunits FTase/GGTaseI-α and FTase-β formed a heterodimer to transfer a farnesyl group from FPP to protein N-dansyl-GCVLS, confirming they are responsible for protein farnesylation in planta.
Abstract
Tripterygium wilfordii is a medicinal plant with a broad spectrum of anti-inflammatory, immunosuppressive and anti-cancer activities. Recently, a number of studies have focused on investigating the biosynthetic pathways of its bioactive compounds, whereas little attention has been paid to the enzymes which play important roles in regulating diverse developmental processes of T. wilfordii. In this study, we report for the first time the identification and characterization of two subunits of farnesyltransferase (FTase), farnesyltransferase/geranylgeranyltransferase I-α (TwFTase/GGTase I-α) and farnesyltransferase-β (TwFTase-β), in this important medicinal plant. Cell-free in vivo assays, yeast two-hybrid (Y2H) and pull-down assays showed that the two subunits interact with each other to form a heterodimer to perform the role of specifically transferring a farnesyl group from FPP to the CAAX-box protein N-dansyl-GCVLS. Furthermore, we discovered that the two subunits had the same cytoplasmic localization pattern and displayed the same tissue expression pattern. These results indicated that we identified a functional TwFTase enzyme which contains two functionally complementary subunits TwFTase/GGTase I-α and TwFTase-β, which provides us promising genetic targets to construct transgenic plants or screen for more adaptable T. wilfordii mutants, which are able to survive in changing environments.






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Ahearn IM, Haigis K, Bar-Sagi D, Philips MR (2011) Regulating the regulator: post-translational modification of RAS. Nat Rev Mol Cell Biol 13:39–51
Bartel P, Chien CT, Sternglanz R, Fields S (1993) Elimination of false positives that arise in using the two-hybrid system. Biotechniques 14:920–924
Beck G, Coman D, Herren E, Ruiz-Sola MA, Rodríguez-Concepción M, Gruissem W, Vranová E (2013) Characterization of the GGPP synthase gene family in Arabidopsis thaliana. Plant Mol Biol 82:393–416
Caldelari D, Sternberg H, Rodríguez-Concepción M, Gruissem W, Yalovsky S (2001) Efficient prenylation by a plant geranylgeranyltransferase-I requires a functional CaaL box motif and a proximal polybasic domain. Plant Physiol 126:1416–1429
Cassidy PB, Dolence JM, Poulter CD (1995) Continuous fluorescence assay for protein prenyltransferases. Methods Enzymol 250:30–43
Cheng Q, Tong Y, Wang Z, Su P, Gao W, Huang L (2017) Molecular cloning and functional identification of a cDNA encoding 4-hydroxy-3-methylbut-2-enyl diphosphate reductase from Tripterygium wilfordii. Acta Pharm Sin B 7:208–214
Chugh R, Sangwan V, Patil SP, Dudeja V, Dawra RK, Banerjee S, Schumacher RJ, Blazar BR, Georg GI, Vickers SM et al (2012) A preclinical evaluation of Minnelide as a therapeutic agent against pancreatic cancer. Sci Transl Med 4:156ra39
Corson TW, Crews CM (2007) Molecular understanding and modern application of traditional medicines: triumphs and trials. Cell 130:769–774
Cutler S, Ghassemian M, Bonetta D, Cooney S, McCourt P (1996) A protein farnesyl transferase involved in abscisic acid signal transduction in Arabidopsis. Science 273:1239–1241
Del SG, Manfioletti G, Schneider C (1989) The CTAB-DNA precipitation method: a common mini-scale preparation of template DNA from phagemids, phages or plasmids suitable for sequencing. Biotechniques 7:514–520
Dozier JK, Khatwani SL, Wollack JW, Wang YC, Schmidt-Dannert C, Distefano MD (2014) Engineering protein farnesyltransferase for enzymatic protein labeling applications. Bioconjug Chem 25:1203–1212
Du F, Fan J, Wang T, Wu Y, Grierson D, Gao Z, Xia Y (2017) Identification of differentially expressed genes in flower, leaf and bulb scale of Lilium oriental hybrid ‘Sorbonne’ and putative control network for scent genes. BMC Genom 18:899
Dutilleul C, Ribeiro I, Blanc N, Nezames CD, Deng XW, Zglobicki P, Palacio Barrera AM, Atehortùa L, Courtois M, Labas V et al (2016) ASG2 is a farnesylated DWD protein that acts as ABA negative regulator in Arabidopsis. Plant Cell Environ 39:185–198
Hagemann A, Müller G, Manthey I, Bachmann HS (2017) Exploring the putative self-binding property of the human farnesyltransferase alpha-subunit. FEBS Lett 591:3637–3648
Hauser F, Li Z, Waadt R, Schroeder JI (2017) SnapShot: abscisic acid signaling. Cell 171:1708
Iwabuchi K, Li B, Bartel P, Fields S (1993) Use of the two-hybrid system to identify the domain of p53 involved in oligomerization. Oncogene 8:1693–1696
Johnson CD, Chary SN, Chernoff EA, Zeng Q, Running MP, Crowell DN (2005) Protein geranylgeranyltransferase I is involved in specific aspects of abscisic acid and auxin signaling in Arabidopsis. Plant Physiol 139:722–733
Manavalan LP, Chen X, Clarke J, Salmeron J, Nguyen HT (2012) RNAi-mediated disruption of squalene synthase improves drought tolerance and yield in rice. J Exp Bot 63:63–75
Manmathan H, Shaner D, Snelling J, Tisserat N, Lapitan N (2013) Virus-induced gene silencing of Arabidopsis thaliana gene homologues in wheat identifies genes conferring improved drought tolerance. J Exp Bot 64:1381–1392
Manolaridis I, Kulkarni K, Dodd RB, Ogasawara S, Zhang Z, Bineva G, Reilly NO, Hanrahan SJ, Thompson AJ, Cronin N et al (2013) Mechanism of farnesylated CAAX protein processing by the intramembrane protease Rce1. Nature 504:301–305
Manzo SG, Zhou ZL, Wang YQ, Marinello J, He JX, Li YC, Ding J, Capranico G, Miao ZH (2012) Natural product triptolide mediates cancer cell death by triggering CDK7-dependent degradation of RNA polymerase II. Cancer Res 72:5363–5373
Northey JG, Liang S, Jamshed M, Deb S, Foo E, Reid JB, McCourt P, Samuel MA (2016) Farnesylation mediates brassinosteroid biosynthesis to regulate abscisic acid responses. Nature Plants 2:16114
Su P, Guan H, Zhang Y, Wang X, Gao L, Zhao Y, Hu T, Zhou J, Ma B, Tu L et al (2017) Probing the single key amino acid responsible for the novel catalytic function of ent-kaurene oxidase supported by NADPH-cytochrome P450 reductases in Tripterygium wilfordii. Front Plant Sci 8:1756
Su P, Guan H, Zhao Y, Tong Y, Xu M, Zhang Y, Hu T, Yang J, Cheng Q, Gao L et al (2018) Identification and functional characterization of diterpene synthases for triptolide biosynthesis from Tripterygium wilfordii. Plant J 93:50–65
Subramani PA, Narala VR, Michael RD, Lomada D, Reddy MC (2015) Molecular docking and simulation of curcumin with Geranylgeranyl Transferase1 (GGTase1) and Farnesyl Transferase (FTase). Bioinformation 11:248–253
Tamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: Molecular evolutionary genetics analysis version 6.0. Mol Biol Evol 30:2725–2729
Titov DV, Gilman B, He QL, Bhat S, Low WK, Dang Y, Smeaton M, Demain AJ, Miller PS, Kugel JF et al (2011) XPB, a subunit of TFIIH, is a target of the natural product triptolide. Nat Chem Biol 7:182–188
Tong Y, Su P, Zhao Y, Zhang M, Wang X, Liu Y, Zhang X, Gao W, Huang L (2015) Molecular cloning and characterization of DXS and DXR genes in the terpenoid biosynthetic pathway of Tripterygium wilfordii. Int J Mol Sci 16:25516–25535
Tu SH (2009) Difficulties and countermeasures in treatment of rheumatoid arthritis with Tripterygium. Chin J Integr Tradit West Med 29:104–105
Wang Y, Ying J, Kuzma M, Chalifoux M, Sample A, McArthur C, Uchacz T, Sarvas C, Wan J, Dennis DT et al (2005) Molecular tailoring of farnesylation for plant drought tolerance and yield protection. Plant J 43:413–424
Wang Y, Beaith M, Chalifoux M, Ying J, Uchacz T, Sarvcs C, Griffiths R, Kuzma M, Wan J, Huang Y (2009) Shoot-specific down-regulation of protein farnesyltransferase (alpha-subunit) for yield protection against drought in canola. Mol Plant 2:191–200
Wong KF, Yuan Y, Luk JM (2012) Tripterygium wilfordii bioactive compounds as anticancer and anti-inflammatory agents. Clin Exp Pharmacol Physiol 39:311–320
Wu JR, Wang LC, Lin YR, Weng CP, Yeh CH, Wu SJ (2017) The Arabidopsis heat-intolerant 5 (hit5)/enhanced response to aba 1 (era1) mutant reveals the crucial role of protein farnesylation in plant responses to heat stress. New Phytol 213:1181–1193
Zhai Q, Zhang X, Wu F, Feng H, Deng L, Xu L, Zhang M, Wang Q, Li C (2015) Transcriptional mechanism of jasmonate receptor COI1-mediated delay of flowering time in Arabidopsis. Plant Cell 27:2814–2828
Zhang M, Su P, Zhou YJ, Wang XJ, Zhao YJ, Liu YJ, Tong YR, Hu TY, Huang LQ, Gao W (2015) Identification of geranylgeranyl diphosphate synthase genes from Tripterygium wilfordii. Plant Cell Rep 34:2179–2188
Zhao YJ, Chen X, Zhang M, Su P, Liu YJ, Tong YR, Wang XJ, Huang LQ, Gao W (2015) Molecular cloning and characterisation of farnesyl pyrophosphate synthase from Tripterygium wilfordii. PloS One 10:e0125415
Zhou ZL, Yang YX, Ding J, Li YC, Miao ZH (2012) Triptolide: structural modifications, structure-activity relationships, bioactivities, clinical development and mechanisms. Nat Prod Rep 29:457–475
Acknowledgements
This research was supported by the National Natural Science Foundation of China (81773830 to W.G.), High-level Teachers in Beijing Municipal Universities in the Period of 13th Five-year Plan (CIT&TCD20170324 to W.G.) and the Key project at central government level: the ability establishment of sustainable use for valuable Chinese medicine resources (2060302 to L.H.).
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PS, LH and WG designed the project; LG, SL, HG, JW, YZ (Zhang), YZ(Zhao) and TH performed the experiments and database analysis; PS, LG and LT wrote the manuscript; JZ, BM and XL interpreted the data; All authors read and approved the final manuscript.
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Communicated by Baochun Li.
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Su, P., Gao, L., Liu, S. et al. Probing the function of protein farnesyltransferase in Tripterygium wilfordii. Plant Cell Rep 38, 211–220 (2019). https://doi.org/10.1007/s00299-018-2363-9
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DOI: https://doi.org/10.1007/s00299-018-2363-9


