Publications

Special Issue

Special Issue

Special Issue

Plant, Cell & Environment published a Special Issue on “Stress Priming, Memory and Signalling in Plants”.

The issue is available online at: https://onlinelibrary.wiley.com/toc/13653040/2019/42/3.

Several CRC 973 PIs contributed to this issue by review articles or original articles. Monika Hilker and Thomas Schmülling served as guest editors.

Review Article

Several CRC 973 PIs published a review article on "Priming and memory of stress responses in organisms lacking a nervous system". You find the article here: https://onlinelibrary.wiley.com/doi/full/10.1111/brv.12215

2020

  • Griese, E., Pineda, A., Pashalidou, F.G., Pizarro Iradi, E., Hilker, M., Dicke, M. and Fatouros, N.E. (2019). Plant responses to butterfly oviposition partly explain preference–performance relationships on different brassicaceous species. Oecologia doi: 10.1007/s00442-019-04590-y.

  • Guerra, T., Schilling, S., Hake, K., Gorzolka, K., Sylvester, F.-P., Conrads, B., Westermann, B. and Romeis, T. (2020). Calcium-dependent protein kinase 5 links calcium-signaling with N-hydroxy-L-pipecolic acid- and SARD1-dependent immune memory in systemic acquired resistance. New Phytol. 225: 310-325, doi: 10.1111/nph.16147.

  • Vyse, K., Penzlin, J., Sergeant, K., Hincha, D.K., Arora, R. and Zuther, E. (2020). Repair of sub-lethal freezing damage in leaves of Arabidopsis thaliana. BMC Plant Biol., doi: 10.1186/s12870-020-2247-3.

2019

  • Bittner, N., Hundacker, J., Achotegui-Castells, A., Anderbrant, O. and Hilker, M. (2019). Defense of Scots pine against sawfly eggs (Diprion pini) is primed by exposure to sawfly sex pheromones. PNAS doi: 10.1073/pnas.1910991116.

  • Brzezinka, K., Altmann, S.and Bäurle, I. (2019). BRUSHY1/TONSOKU/MGOUN3 is required for heat stress memory. Plant Cell Environ. 42: 765-775, doi: 10.1111/pce.13365.

  • Cortleven, A., Leuendorf, J.E., Frank, M., Bolt, S., Pezzetta, D. and Schmülling, T. (2019). Cytokinin action in response to abiotic and biotic stresses in plants. Plant Cell Environ. 42: 998-1018, doi.org/10.1111/pce.13494.

  • Elabed, H., González-Tortuero, E., Ibacache-Quiroga, C., Bakhrouf, A., Johnston, P., Kamel G., Blázquez, J. and Rodríguez-Rojas, A. (2019). Seawater salt-trapped Pseudomonas Aeruginosa survives for years and gets primed for salinity tolerance. BMC Microbiol. 19: 142, doi: 10.1186/s12866-019-1499-2.

  • El Shazely, B., Urbański, A., Johnston, P. R. and Rolff, J. (2019). In Vivo exposure of insect AMP resistant Staphylococcus aureus to an insect immune system. Insect Bioch. Mol. Biol. 110: 60–68, doi: 10.1016/j.ibmb.2019.04.017.

  • Friedrich, T., Faivre, L., Bäurle, I. and Schubert, D. (2019). Chromatin‐based mechanisms of temperature memory in plants. Plant Cell Environ. 42: 756-764, doi: 10.1111/pce.13373.

  • Fritsch, V.N., Loi, V.V., Busche, T., Sommer, A., Nürnberg, D.J., Tedin, K., Kalinowski, J., Bernhardt, J., Fulde, M. and Antelmann, H. (2019). The MhqR repressor confers resistance to quinone-like antimicrobials in Staphylococcus aureus. Antioxid. Redox Signal. 31: 1235-1252, doi: 10.1089/ars.2019.7750.

  • Guerra, T., Schilling, S., Hake, K., Gorzolka, K., Sylvester, F.-P., Conrads, B., Westermann, B. and Romeis, T. (2019). Calcium-dependent protein kinase 5 links calcium-signaling with N-hydroxy-L-pipecolic acid- and SARD1-dependent immune memory in systemic acquired resistance. New Phytol. 225: 310-325, doi: 10.1111/nph.16147.

  • Hilker, M. and Schmülling, T. (2019). Stress priming, memory, and signalling in plants. Plant Cell Environ. 42: 753-761 doi: 10.1111/pce.13526.

  • Kafle, D. and Wurst, S. (2019). Legacy effects of herbivory enhance performance and resistance of progeny plants. J. Ecol. 107: 58-68, doi: 10.1111/1365-2745.13038.

  • Lortzing, V., Oberländer, J., Lortzing, T., Tohge, T., Steppuhn, A., Kunze, R. and Hilker, M. (2019). Insect egg deposition renders plant defense against hatching larvae more effective in a salicylic acid-dependent manner. Plant Cell Environ. 42: 1019-1032, doi: 10.1111/pce.13447.

  • Loi, V.V., Huyen, N.T.T., Busche, T., Tung, Q.N., Gruhlke, M.C.H., Kalinowski, J., Bernhardt, J., Slusarenko, A.J., and Antelmann, H. (2019). Staphylococcus aureus responds to allicin by global S-thioallylation - Role of the Brx/BSH/YpdA pathway and the disulfide reductase MerA to overcome allicin stress. Free Radic. Biol. Med. 139: 55-69, doi: 10.1016/j.freeradbiomed.2019.05.018.

  • Ma, X., Balazadeh, S. and Mueller-Roeber, B. (2019). Tomato fruit ripening factor NOR controls leaf senescence. J. Exp. Bot. 70: 2727-2740, doi: 10.1093/jxb/erz098.

  • Mikulski, P., Hohenstatt, M.L., Farrona, S., Smaczniak, C., Stahl, Y.S., Kalyanikrishna, Kaufmann, K., Angenent, G. and Schubert, D. (2019). The chromatin-associated protein PWO1 interacts with plant nuclear lamin-like components to regulate nuclear size. Plant Cell: 1141–1154, doi: 10.1105/tpc.18.00663.

  • Oberländer, J., Lortzing, V., Hilker, M. and Kunze, R. (2019). The differential response of cold- experienced Arabidopsis thaliana to larval herbivory benefits an insect generalist, but not a specialist. BMC Plant Biol. 19: 338, doi: 10.1186/s12870-019-1943-3.

  • Ratzmann, G., Meinzer, F.C. and Tietjen, B. (2019). Iso/anisohydry: still a useful concept. Trends Plant Sci.24: 191-194, doi: 10.1016/j.tplants.2019.01.001.

  • Ratzmann, G., Zakharova, L. and Tietjen, B. (2019). Optimal leaf water status regulation of plants in drylands. Sci. Rep. 9: 3768, doi: 10.1038/s41598-019-40448-2.

  • Rillig, M.C., Bonneval, K. and Lehmann, J. (2019) Sounds of soil: A new world of interactions under out feet? Soil Syst. 3: 45. doi: 10.3390/soilsystems3030045.

  • Rodríguez-Rojas, A., Kim, J., Johnston, P., Makarova, O., Eravci, M., Weise, C., Hengge, R. and Rolff, J. (2019). Non-lethal oxidative stress boosts bacterial survival and evolvability under lethal exposure. bioRxiv doi: 10.1101/575134.

  • Ryo, M., Aguilar-Trigueros, C.A., Pinek, L., Muller, L.A.H. and Rillig M.C. (2019). Basic principles of temporal dynamics. Trends Ecol. Evol. 34: 723-733, doi: 10.1016/j.tree.2019.03.007.

  • Schubert, D. (2019). Evolution of Polycomb-group function in the green lineage. F1000Research 8: 268, doi: 10.12688/f1000research.16986.1.

  • Schwachtje, J., Whitcomb, S.J., Firmino, A.A.P., Zuther, E., Hincha, D.K. and Kopka, J. (2019) Induced, imprinted, and primed responses to changing environments: Does metabolism store and process information? Front. Plant Sci. 10:106, doi: 10.3389/fpls.2019.00106.

  • Sedaghatmehr, M., Thirumalaikumar, V. P., Kamranfar, I., Marmagne, A., Masclaux-Daubresse, C. and Balazadeh, S. (2018). A regulatory role of autophagy for resetting the memory of heat stress in plants. Plant Cell Environ. 42: 1053-1063, doi: 10.1111/pce.13426.

  • Szymczak, A., Ryo, M. and Rillig, M.C. (2019). Diversity of responses of soil saprobic fungi to recurring heat   events. bioRxiv, doi: 10.1101/733923.

  • Takahashi, D., Gorka, M., Erban, A., Graf, A., Kopka, J., Zuther, E. and Hincha, D.K. (2019). Both cold and sub-zero acclimation induce cell wall modification and changes in the extracellular proteome in Arabidopsis thaliana. Sci. Rep. 9: 2289, doi: 10.1038/s41598-019-38688-3.

  • van Buer, J., Prescher, A. and Baier M. (2019). Cold-priming of chloroplast ROS signalling is developmentally regulated and is locally controlled at the thylakoid membrane. Sci. Rep. 9: 3022, doi: 10.1038/s41598-019-39838-3.

  • Vyse, K., Faivre, L., Romich, M., Pagter, M., Schubert, D., Hincha, D.K. and Zuther, E. (2019). Transcriptional and post-transcriptional regulation and transcriptional memory of chromatin regulators in response to low temperature. bioRxiv http://dx.doi.org/10.1101/757179.

  • Vyse, K., Pagter, M., Zuther, E. and Hincha, D.K. (2019). Deacclimation after cold acclimation - a crucial, but widely neglected part of plant winter survival. J. Exp. Botany 70: 4595-4604, doi: 10.1093/jxb/erz229.

  • Wesener, F. and Tietjen, B. (2019). Primed to be strong, primed to be fast: modeling benefits of microbial stress responses. FEMS Microbiol. Ecol., fiz114, doi: 10.1093/femsec/fiz114.

  • Zuther, E., Schaarschmidt, S., Fischer, A., Erban, A., Pagter, M., Mubeen, U., Giavalisco, P., Kopka, J., Sprenger, H. and Hincha, D.K. (2019).Molecular signatures associated with increased freezing tolerance due to low temperature memory in Arabidopsis. Plant Cell Environ. 42: 854-873, doi: 10.1111/pce.13502.

2018

  • Altmann, S., Muino, J.M., Lortzing, V., Brandt, R., Himmelbach, A., Altschmied, L. and Hilker, M. (2018). Transcriptomic basis for reinforcement of elm anti-herbivore defense mediated by inect egg deposition. Mol. Ecol. 27: 4901-4915, doi: 10.1111/mec.14900.

  • Auevechanichkul, N., Lintermann, R. and Wirthmueller, L. (2018). Production of magnetic GFP affinity beads. Protocol on Figshare, doi: 10.1002/pro.519.

  • Baier, M., Bittner, A., Prescher, A. and van Buer, J. (2018). Preparing plants for improved cold tolerance by priming. Plant Cell Environ. 42: 776-794, doi: 10.1111/pce.13394.

  • Baldauf, S., Ladrón de Guevara, M., Maestre, F.T. and Tietjen, B. (2018). Soil moisture dynamics under two rainfall frequency treatments drive early spring CO2 gas exchange of lichen-dominated biocrusts in central Spain. PeerJ. 6: e5904, doi: 10.7717/peerj.5904.

  • Brzezinka, K., Altmann, S. and Bäurle, I. (2018). BRUSHY1/TONSOKU/MGOUN3 is required for heat stress memory. Plant Cell Environ. 42: 765-775, doi: 10.1111/pce.13365.

  • Chen, C., De Masi, R., Lintermann, R. and Wirtmueller, L. (2018). Nuclear import of Arabidopsis poly (ADP-ribose) polymerase 2 is mediated by importin-α and a nuclear localization sequence located between the predicted SAP domains. Front. Plant Sci. 9: 1581, doi: 10.3389/fpls.2018.01581.

  • Cortleven, A., Leuendorf, J. E., Frank, M., Pezzetta, D., Bolt, S. and Schmülling, T. (2018). Cytokinin action in response to abiotic and bioticstress in plants. Plant Cell Environ. 42: 998–1018, doi: 10.1111/pce.13494.

  • Drok, S., Bandoly, M., Stelzer, S., Lortzing, T. and Steppuhn, A. (2018). Moth oviposition shapes the species-specific transcriptional and phytohormonal response of Nicotiana attenuata to larval feeding. Sci. Rep. 8: 10249, doi: 10.1038/s41598-018-28233-z.

  • Etemadi, M., Zuther, E., Müller, H., Hincha, D.K. and Berg, G. (2018). Ecotype-dependent response of bacterial communities associated with Arabidopsis to cold acclimation. Phytobiomes 2: 3-13, doi: 10.1094/PBIOMES-04-17-0015-R.

  • Geuss, D., Lortzing, T., Schwachtje, J., Kopka, J. and Steppuhn, A. (2018). Oviposition by Spodoptera exigua on Solanum dulcamara alters the plant's response to herbivory and impairs larval performance. Internatl. J. Mol. Sci. 19: 4008, doi: 10.3390/ijms19124008.

  • Hake, K. and Romeis, T. (2018). Protein kinase‐mediated signaling in priming: immune signal initiation, propagation, and establishment of long‐term pathogen resistance in plants. Plant Cell Environ. 42: 898-911, doi: 10.1111/pce.13429.

  • Hohenstatt, M.L., Mikulski, P., Komarynets, O. , Klose, C., Kycia, I., Jeltsch, A., Farrona, S. and Schubert, D. (2018). PWWP-DOMAIN INTERACTOR OF POLYCOMBS1 interacts with polycomb-group proteins and histones and regulates Arabidopsis flowering and development. Plant Cell 30: 117-133, doi: 10.1105/tpc.17.00117.

  • Imber, M., Huyen, N.T.T., Pietrzyk-Brzezinska, A.J., Loi, V.V., Hillion, M., Bernhardt, J., Thärichen, L., Kolšek, K., Saleh, M., Hamilton, C.J., Adrian, L., Gräter, F., Wahl, M.C. and Antelmann H. (2018). Protein S-bacillithiolation functions in thiol protection and redox regulation of the glyceraldehyde-3-phosphate dehydrogenase gap in Staphylococcus aureus under hypochlorite stress. Antioxid. Redox Signal. 28: 410-430, doi: 10.1089/ars.2016.6897.

  • Imber, M., Loi, V.V., Reznikov, S., Fritsch, V.N., Pietrzyk-Brzezinska, A.J., Prehn, J., Hamilton, C.J., Wahl, M.C., Bronowska, A.K. and Antelmann, H. (2018). The aldehyde dehydrogenase AldA contributes to the hypochlorite defense and is redox-controlled by protein S-bacillithiolation in Staphylococcus aureus. Redox Biol. 15: 557-568, doi: 10.1016/j.redox.2018.02.001.

  • Jouvet, L., Rodríguez-Rojas, A. and Steiner, U. (2018). Demographic variability and heterogeneity among individuals within and among clonal bacteria strains. Oikos 127: 728–737, doi: 10.1111/oik.04292.

  • Kamranfar, I., Xue, G.P., Tohge, T., Sedaghatmehr, M., Fernie, A.R., Balazadeh, S. and Mueller-Roeber, B.(2018). Transcription factor RD26 is a key regulator of metabolic reprogramming during dark-induced senescence. New Phytol. 218: 1543-1557, doi: 10.1111/nph.15127.

  • Kudla, J., Becker. D., Grill, E., Hedrich, R., Hippler, M., Kummer, U., Parniske, M., Romeis, T. and Schumacher, K. (2018). Advances and current challenges in calcium signaling. New Phytol. 218:414-431, doi: 10.1111/nph.14966.

  • Liu, H-C., Lämke, J., Lin, S-Y., Hung, M-J., Liu, K.-M., Charng, Y.-Y. and Bäurle, I. (2018). Distinct heat shock factors and chromatin modifications mediate the organ-autonomous transcriptional memory of heat stress. Plant J. 95: 401-413, doi: 10.1111/tpj.13958.

  • Loi, V.V., Busche, T., Bernhardt, J., Tedin, K., Wollenhaupt, J., Huyen, N.T.T., Weise, C., Kalinowski, J., Wahl, M., Fulde, M. and Antelmann, H. (2018). Redox-sensing under hypochlorite stress and infection conditions by the Rrf2-family repressor HypR in Staphylococcus aureus. Antioxid. Redox Sign. 29: 615-636, doi: 10.1089/ars.2017.7354.

  • Lortzing, V., Oberländer, J., Lortzing, T., Tohge, T., Steppuhn, A., Kunze, R. and Hilker, M. (2018). Insect egg deposition renders plant defense against hatching larvae more effective in a salicylic acid-dependent manner. Plant Cell Environ. 42: 1019–1032, doi: 10.1111/pce.13447.

  • Makarova, O., Johnston, P., Rodriguez-Rojas, A., El Shazely, B., Moreno-Morales, J. and Rolff, J. (2018). Genomics of experimental adaptation of Staphylococcus aureus to a natural combination of insect antimicrobial peptides. Sci. Rep. 8: 15359, doi: 10.1038/s41598-018-33593-7.

  • Nietzsche, M., Guerra, T., Alseekh, S., Wiermer, M., Sonnewald, S., Fernie, A.R. and Börnke, F. (2018). STOREKEEPER RELATED 1/G-element binding protein (STKR1) interacts with protein kinase SnRK1. Plant Physiol. 176: 1773-1792, doi: 10.1104/pp.17.01461.

  • Omidbakhshfard, M.A., Fujikura, U., Olas, J.J., Xue, G.-P., Balazadeh, S. and Mueller-Roeber, B. (2018). GROWTH-REGULATING FACTOR 9 negatively regulates Arabidopsis leaf growth by controlling ORG3 and restricting cell proliferation in leaf primordia. PLoS Genet. 14: e1007484, doi: 10.1371/journal.pgen.1007484.

  • Rodriguez-Rojas, A., Moreno-Morales, J., Mason, A.J. and Rolff, J. (2018). Cationic antimicrobial peptides do not change recombination frequency in Escherichia coli. Biol. Lett. 14: 20180006, doi: 10.1098/rsbl.2018.0006.

  • Schwachtje, J., Fischer, A., Erban, A. and Kopka, J. (2018). Primed primary metabolism in systemic leaves: a functional systems analysis. Sci. Rep. 8: 216, doi: 10.1038/s41598-017-18397-5.

  • Sprenger, H., Erban, A., Seddig, S., Rudack, K., Thalhammer, A., Le, M.Q., Walther, D., Zuther, E., Köhl, K., Kopka, J. and Hincha, D.K. (2018). Metabolite and transcript markers for the prediction of potato drought tolerance. Plant Biotechnol. J. 16: 939-950, doi: 10.1111/pbi.12840.

  • Thirumalaikumar, V.P., Devkar, V., Mehterov, N., Ali, S., Ozgur, R., Turkan, I., Mueller-Roeber, B. and Balazadeh, S. (2018). NAC transcription factor JUNGBRUNNEN1 enhances drought tolerance in tomato. Plant Biotechnol. J. 16: 354-366, doi: 10.1111/pbi.12776.

  • Tung, Q.N., Linzner, N., Loi, V.V. and Antelmann, H. (2018). Application of genetically encoded redox biosensors to measure dynamic changes in the glutathione, bacillithiol and mycothiol redox potentials in pathogenic bacteria. Free Radic. Biol. Med. 128: 84-96, doi: 10.1016/j.freeradbiomed.2018.02.018.

  • Veresoglou, S.D., Wang, D., Andrade-Linares, D.R., Hempel, S. and Rillig, M.C. (2018). Fungal decision to exploit or explore depends on growth rate. Microb. Ecol. 75: 289-292, doi: 10.1007/s00248-017-1053-4.

  • Voirol, L.R.P., Frago, E., Kaltenpoth, M., Hilker, M. and Fatouros, N.E. (2018). Bacterial symbionts in Lepidoptera: Their diversity, transmission, and impact on the host. Front. Microbiol. 9: 556, doi: 10.3389/fmicb.2018.00556.

  • Weinhold, A. (2018). Transgenerational stress-adaption: an opportunity for ecological epigenetics. Plant Cell Rep. 37: 3-9, doi: 10.1007/s00299-017-2216-y.

  • Yang, G., Wagg, C., Veresoglou, S.D., Hempel, S. and Rillig, M.C. (2018). How soil biota drive ecosystem stability. Trends Plant Sci. 23: 1057-1067, doi: 10.1016/j.tplants.2018.09.007.

  • Yu, G., Baeder, D., Regoes, R., Rolff, J. (2018). Predicting drug resistance evolution: antimicrobial peptides vs. antibiotics. Proc. R. Soc. Lond. B. 285: 20172687, doi: 10.1098/rspb.2017.2687.

  • Zuther, E., Schaarschmidt, S., Fischer, A., Erban, A., Pagter, M., Mubeen, U., Giavalisco, P., Kopka, J., Sprenger, H. and Hincha, D. (2018). Molecular determinants of increased freezing tolerance due to low temperature memory in Arabidopsis. Plant Cell Environ. 42: 854–873, doi: 10.1111/pce.13502.

2017

  • Andersen, U.B., Kjaer, K.H., Erban, A., Alpers, J., Hincha, D.K., Kopka, J., Zuther, E. and Pagter, M. (2017). Impact of seasonal warming on overwintering and spring phenology of blackcurrant. Environ. Exp. Bot. 140: 96-109, doi: 10.1016/j.envexpbot.2017.06.005.

  • Bäurle, I. (2017). Can't remember to forget you: Chromatin-based priming of somatic stress responses. Semin. Cell Dev. Biol. 83: 133-139, doi: 10.1016/j.semcdb.2017.09.032.

  • Bolt, S., Zuther, E., Zintl, S., Hincha, D. K. and Schmülling, T. (2017). ERF105 is a transcription factor gene of Arabidopsis thaliana required for freezing tolerance and cold acclimation. Plant Cell Environ. 40: 108-120, doi: 10.1111/pce.12838.

  • Bremer, A., Kent, B., Hauß, T., Thalhammer, A., Yepuri, N.R., Darwish, T.A., Garvey, C.J., Bryant, G. and Hincha, D.K. (2017). Intrinsically disordered stress protein COR15A resides at the membrane surface during dehydration. Biophys. J. 113: 572-579, doi: 10.1016/j.bpj.2017.06.027.

  • Cvetkovic, J., Mueller, K. and Baier, M. (2017). The effect of cold priming on the fitness of Arabidopsis thaliana accessions under natural and controlled conditions. Sci. Rep. 7: 44055, doi: 10.1038/srep44055.

  • Geuss, D., Stelzer, S., Lortzing, T. and Steppuhn, A. (2017). An ovicidal response of Solanum dulcamara to insect oviposition. Plant Cell Environ. 40: 2663-2677, doi: 10.1111/pce.13015.

  • Griese, E., Dicke, M., Hilker, M. and Fatouros, N.E. (2017). Plant response to butterfly eggs: inducibility, severity and success of egg-killing leaf necrosis depends on plant genotype and egg clustering. Sci. Rep. 7: 7316, doi: 10.1038/s41598-017-06704-z.

  • Hedtmann, C., Guo, W., Reifschneider, E., Heiber, I., Hiltscher, H., van Buer, J., Barsch, A., Niehaus, K., Rowan, B., Lortzing, T., Steppuhn, A. and Baier, M. (2017). The plant immunity regulating F-Box protein CPR1 supports plastid function in absence of pathogens. Front. Plant Sci. 8: 1650, doi: 10.3389/fpls.2017.01650.

  • Kafle, D., Hänel, A., Lortzing, T., Steppuhn, A. and Wurst, S. (2017). Sequential above- and belowground herbivory modifies plant responses depending on herbivore identity. BMC Ecol. 17: 5, doi: 10.1186/s12898-017-0115-2.

  • Kleinmanns, J.A., Schatlowski, N., Heckmann, D. and Schubert D. (2017). BLISTER regulates polycomb-target genes, represses stress-regulated genes and promotes stress responses in Arabidopsis thaliana. Front Plant Sci. 8: 1530, 1-14, doi: 10.3389/fpls.2017.01530.

  • Lämke, J. and Bäurle, I. (2017). Epigenetic and chromatin-based mechanisms in environmental stress adaptation and stress memory in plants. Genome Biol. 18: 124, doi: 10.1186/s13059-017-1263-6.

  • Lira, B., Gramegna, G., Trench, B., Alves, F., Silva, É., Silva, G., Thirumalaikumar, V.P., Lupi, A., Demarco, D., Nogueira, F., Balazadeh, S., Freschi, L. and Rossi, M. (2017). Manipulation of a senescence-associated gene improves fleshy fruit yield in Solanum lycopersicum. Plant Physiol. 175: 77-91, doi: 10.1104/pp.17.00452.

  • Liu, N., Hake, K., Wang, W., Zhao, T., Romeis T. and Tang, D. (2017). CALCIUM‐DEPENDENT PROTEIN KINASE5 associates with the truncated NLR protein TIR‐NBS2 to contribute to exo70B1‐mediated immunity. Plant Cell 29: 746–759, doi: 10.1105/tpc.16.00822.

  • Lortzing, T., Firtzlaff, V., Nguyen, D., Rieu, I., Stelzer, S., Schad, M., Kallarackal, J. and Steppuhn, A. (2017). Transcriptomic responses of Solanum dulcamara to natural and simulated herbivory. Mol. Ecol. Res.17: 196-211, doi: 10.1111/1755-0998.12687.

  • Mikulski,  P., Komarynets, O., Fachinelli, F., Weber, A.P.M. and Schubert D. (2017). Characterization of the Polycomb-group mark H3K27me3 in unicellular algae. Front Plant Sci. 8: 607, doi: 10.3389/fpls.2017.00607.

  • Motlagh, S.E., Ribone, P.A., Thirumalaikumar, V.P., Allu, A.D., Chan, R.L., Mueller-Roeber, B. and Balazadeh, S. (2017). JUNGBRUNNEN1 confers drought tolerance downstream of the HD-Zip I transcription factor AtHB13. Front. Plant Sci. 8: 2118, doi: 10.3389/fpls.2017.02118.

  • Nitschke, S., Cortleven, A. and Schmülling, T. (2017). Novel stress in plants by altering the photoperiod. Trends in Plant Sci. 22: 913-916, doi: 10.1016/j.tplants.2017.09.005.

  • Pagter, M., Alpers, J., Erban, A., Kopka, J., Zuther, E. and Hincha, D. K. (2017). Rapid transcriptional and metabolic regulation of the deacclimation process in cold acclimated Arabidopsis thaliana. BMC Genomics 18: 731, doi: 10.1186/s12864-017-4126-3.

  • Pappas, M.L., Broekgaarden, C., Broufas, G.D., Kant, M.R., Messelink, G.J., Steppuhn, A., Wäckers, F.L. and van Dam, N.M. (2017). Induced plant defences in biological control: a double-edged sword. Pest Managem. Sci. 73: 1780-1788, doi: 10.1002/ps.4587.

  • Schäfer, M., Brütting, C., Xu, S., Ling, Z., Steppuhn, A., Baldwin, I.T. and Schuman, M.C. (2017). NaMYB8 regulates distinct, optimally distributed herbivore defense traits. J. Integr. Plant Biol. 12: 844-885, doi: 10.1111/jipb.12593.

2016

  • Andrade-Linares, D.R., Veresoglou, S.D. and Rillig, M.C. (2016). Temperature priming and memory in soil filamentous fungi. Fungal Ecol. 21: 10-15, doi: 10.1016/j.funeco.2016.02.002.

  • Andrade-Linares, D.R., Lehmann, A. and Rillig, M.C. (2016). Microbial stress priming – a meta-analysis. Environ. Microbiol. 18: 1277-1288, doi: 10.1111/1462-2920.13223.

  • Anjum, N.A., Khan, N.A., Sofo, A., Baier, M. and Kizek, R. (2016). Redox homeostasis managers in plants under environmental stresses. Front. Environ. Sci. 4: 35, doi: 10.3389/fenvs.2016.00035.

  • Austel, N., Eilers, E.J., Meiners, T. and Hilker, M. (2016). Elm leaves “warned” by insect egg deposition reduce survival of hatching larvae by a shift in their quantitative leaf metabolite pattern. Plant Cell Environ. 39: 366-376, doi 10.1111/pce.12619.

  • Bandoly, M., Grichnik, R., Hilker, M. and Steppuhn, A. (2016). Priming of anti-herbivore defence in Nicotiana attenuata by insect oviposition: Herbivore specific effects. Plant Cell Environ. 39: 848-859, doi: 10.1111/pce.12677.

  • Bandoly, M. and Steppuhn, A. (2016). Bioassays to investigate the effects of insect oviposition on a plant’s resistance to herbivores. BioProtocol. 6: e1823, doi: 10.21769/BioProtoc.1823.

  • Bandoly, M. and Steppuhn, A. (2016). A push-button: Spodoptera exigua oviposition on Nicotiana attenuata dose-independently primes the feeding-induced plant defence. Plant Signal. Behav. 11: e1114198, doi: 10.1080/15592324.2015.1114198.

  • Bäurle I. (2016). Plant heat adaptation: priming in response to heat stress. F1000Research (F1000 Faculty Rev.): 694, doi: 10.12688/f1000research.7526.1.

  • Brzezinka, K., Altmann, S., Czesnick, H., Nicolas, P., Górka, M., Benke, E., Kabelitz, T., Jähne, F., Graf, A., Kappel, C. and Bäurle, I. (2016). Arabidopsis FORGETTER1 mediates stress-induced chromatin memory through nucleosome remodeling. eLife 5: e17061, doi: 10.7554/eLife.17061.

  • Cortleven, A., Marg, I., Yamburenko, M.V., Schlicke, H., Hill, K., Grimm, B., Schaller, E.G. and Schmülling, T. (2016). Cytokinin regulates the etioplast-chloroplast transition through the two-component signaling system and activation of chloroplast-related genes. Plant Physiol. 172: 464-478, doi: 10.1104/pp.16.00640.

  • Firtzlaff, V., Oberländer, J., Geiselhardt, S., Hilker, M. and Kunze, R. (2016). Pre-exposure of Arabidopsis to the abiotic or biotic environmental stimuli ´chilling´ or ´insect eggs´ exhibits different transcriptomic responses to herbivory. Sci. Rep. 6: 28544, doi: 10.1038/srep28544.

  • Hilker, M. and Fatouros, N.E. (2016). Resisting the onset of herbivory: plants perceive and respond to insect eggs. Curr. Opin. Plant Biol. 32: 9-16, doi: 10.1016/j.pbi.2016.05.003.

  • Hilker, M., Schwachtje, J., Baier, M., Balazadeh, S., Bäurle, I., Geiselhardt, S., Hincha, D.K., Kunze, R., Mueller-Roeber, B., Rillig, M.C., Romeis, T., Schmülling, T., Steppuhn, A., van Dongen, J., Whitcomb, S.J., Wurst, S., Zuther, E. and Kopka, J. (2016). Priming and memory of stress responses in organisms lacking a nervous system. Biol. Rev. 91: 1118-1133, doi: 10.1111/brv.12215.

  • Juszczak, I., Cvetkovic, J., Zuther, E., Hincha, D.K. and Baier, M. (2016). Natural variation of cold deacclimation correlates with variation of cold-acclimation of the plastid antioxidant system in Arabidopsis thaliana accessions. Front. Plant Sci. 7: 305, doi: 10.3389/fpls.2016.00305.

  • Kabelitz, T., Brzezinka, K., Friedrich, T., Gorka, M., Graf, A., Kappel, C. and Bäurle, I. (2016). A JUMONJI protein with E3 ligase and histone H3 binding activities affects transposon silencing in Arabidopsis. Plant Physiol. 171: 344-358, doi: 10.1104/pp.15.01688.

  • Lämke, J., Brzezinka, K., Altmann, S. and Bäurle, I. (2016). A hit-and-run HSF governs sustained histone methylation and transcriptional memory after heat stress. EMBO J. 35: 162-175, doi: 10.15252/embj.201592593.

  • Lämke, J., Brzezinka, K. and Bäurle, I. (2016). HSFA2 orchestrates transcriptional dynamics after heat stress in Arabidopsis thaliana. Transcription 7: 111-114, doi: 10.15252/embj.201592593.

  • Lortzing, T., Calf, O.W., Böhlke, M., Schwachtje, J., Kopka, J., Geuss, D., Kosanke, S., van Dam, N.M. and Steppuhn, A. (2016). Plant-bleeding for defence: Extrafloral nectar secretion from wounds of Solanum dulcamara. Nat. Plants 2: 16056, doi: 10.15252/embj.201592593.

  • Lortzing, T. and Steppuhn, A. (2016). Jasmonate signalling in plants shapes plant-insect interaction ecology. Curr. Opin. Insect Sci. 14: 32-39, doi: 10.1016/j.cois.2016.01.002.

  • Makarova, O., Rodriguez-Rojas, A., Erevci, M., Weise, C., Dobson, A., Johnston, P. and Rolff, J. (2016). Longlasting immunity and persistent infection in insects revisited. Phil. Trans. Roy. Soc. B. 371: 1695, doi: 10.1098/rstb.2015.0296.

  • Nitschke, S., Cortleven, A., Iven, T., Feussner, I., Havaux, M., Riefler, M. and Schmülling, T. (2016). Circadian stress regimes affect the circadian clock and cause jasmonic acid-dependent cell death in cytokinin-deficient Arabidopsis plants. Plant Cell 28: 1616-39, doi: 10.1105/tpc.16.00016.  

  • Popova, A.V. and Hincha, D.K. (2016). Effects of flavonol glycosides on liposome stability during freezing and drying. Biochim. Biophys. Acta - Biomem. 1858: 3050-3060, doi: 10.1016/j.bbamem.2016.09.020.

  • Schulz, E., Tohge, T., Zuther, E., Fernie, A.R. and Hincha, D.K. (2016). Flavonoids are determinants of freezing tolerance and cold acclimation in Arabidopsis thaliana. Sci. Rep. 6: 34027, doi: 10.1038/srep34027.

  • Sedaghatmehr, M., Mueller-Roeber, B. and Balazadeh, S. (2016). The plastid metalloprotease FtsH6 and small heat shock protein HSP21 jointly regulate thermomemory in Arabidopsis. Nat. Comm. 7: 12439, doi: 10.1038/ncomms12439.

  • Shahnejat-Bushehri, S., Tarkowska, D., Sakuraba, Y. and Balazadeh, S. (2016). Arabidopsis NAC transcription factor JUB1 regulates GA/BR metabolism and signalling. Nat. Plants 2: 16013, doi: 10.1038/nplants.2016.13.

  • Üstün, S., Sheikh, A., Gimenez-Ibanez, S., Jones, A., Ntoukakis, V. and Börnke, F. (2016). The proteasome acts as a hub for plant immunity and is targeted by pseudomonas type III effectors. Plant Physiol. 172: 1941-1958, doi: 10.1104/pp.16.00808.

  • van Buer, J., Cvetkovic, J. and Baier, M. (2016). Cold regulation of plastid ascorbate peroxidases serves as a priming hub controlling ROS signaling in Arabidopsis thaliana. BMC Plant Biol. 16:163,  doi: 10.1186/s12870-016-08536-7. 10.

2015

  • Aguilar-Trigueros, C.A., Hempel, S., Powell, J.R., Anderson, I.C., Antonovics, J., Bergmann, J., Cavagnaro, T.R., Chen, B.D., Hart, M.M., Klironomos, J., Petermann, J.S., Verbruggen, E., Veresoglou, S.D. and Rillig, M.C. (2015). Branching out: towards a trait-based understanding of fungal ecology. Fung. Biol. Rev. 29: 34-41, http://dx.doi.org/10.1016/j.fbr.2015.03.001.

  • Austel, N., Reinecke, A., Björkman, C., Hilker, M. and Meiners, T. (2015). Phenotypic plasticity in a willow leaf beetle depends on host plant species: Release and recognition of beetle odors. Chem. Sens. 40: 109-124, doi: 10.1111/tpj.12918.

  • Bandoly, M., Hilker, M. and Steppuhn, A. (2015). Oviposition by Spodoptera exigua on Nicotiana attenuata primes induced plant defence against larval herbivory. Plant J. 83: 661-672, doi: 10.1111/pce.12677.

  • Brenner, W.G. and Schmülling, T. (2015). Summarizing and exploring data of a decade of cytokinin-related transcriptomics. Front. Plant Sci. 6: 29, doi: 10.3389/fpls.2015.00029.

  • Büchel, K., Fenning, T., Gershenzon, J., Hilker, M. and Meiners, T. (2015). Elm defence against herbivores and pathogens: Morphological, chemical and molecular regulation aspects. Phytochem. Rev. 15: 961-983, doi: 10.1007/s11101-015-9442-0.

  • del Prete, S., Mikulski, P., Schubert, D. and Gaudin, V. (2015). One, two, three: polycomb proteins hit all dimensions of gene gegulation. Genes 6: 520-542, doi: 10.3390/genes6030520.

  • Garapati, P., Feil, R., Lunn, J.E., van Dijck, P., Balazadeh, S. and Mueller-Roeber, B. (2015). Transcription factor Arabidopsis activating Factor1 integrates carbon starvation responses with trehalose metabolism. Plant Physiol. 169: 379-390, doi: 10.1104/pp.15.00917.

  • Garapati, P., Xue, G.-P., Munné-Bosch, S. and Balazadeh, S. (2015). Transcription factor ATAF1 in Arabidopsis promotes senescence by direct regulation of key chloroplast maintenance and senescence transcriptional cascades. Plant Physiol. 168: 1122-1139, doi: 10.1104/pp.15.00567.

  • Hilker, M. and Fatouros, N.E. (2015). Plant responses to insect egg deposition. Annu. Rev. Entomol. 60: 493–515, doi: 10.1146/annurev-ento-010814-020620.

  • Le, M.Q., Pagter, M. and Hincha, D.K. (2015). Global changes in gene expression, assayed 25 by microarray hybridization and quantitative RT-PCR, during acclimation of three Arabidopsis thaliana accessions to sub-zero temperatures after cold acclimation. Plant Mol. Biol. 87: 1-15, doi: 10.1007/s11103-014-0256-z.

  • Matschi, S., Hake, K., Herde, M., Hause, B. and Romeis, T. (2015). Calcium-dependent protein kinase CPK28 regulates growth by stage-specific alteration of JA levels independent of 20 defense. Plant Cell 27: 591-606, doi: 10.1105/tpc.15.00024.

  • Monaghan, J., Matschi, S., Romeis, T. and Zipfel, C. (2015). The calcium-dependent protein kinase CPK28 negatively regulates BIK1-mediated PAMP-induced calcium burst. Plant Signal. Behav. 10: e1018497, doi: 10.1080/15592324.2015.1018497.

  • Pashalidou, F.G., Frago, E., Griese, E., Poelman, E.H., van Loon, J.J.A., Dicke, M. and Fatouros, N.E. (2015). Early herbivore alert matters: plant-mediated effects of egg deposition on higher trophic levels benefit plant fitness. Ecol. Lett. 18: 927-936, doi: 10.1111/ele.12470.

  • Petrov, V., Hille, J., Mueller-Roeber, B. and Gechev, T.S. (2015). ROS-mediated abiotic stress induced programmed cell death in plants. Plant Physiol. 6: 69, doi: 10.3389/fpls.2015.00069.

  • Popova, A.V., Rausch, S., Hundertmark, M., Gibon, Y. and Hincha, D.K. (2015). The intrinsically disordered protein LEA7 from Arabidopsis thaliana protects the isolated enzyme lactate dehydrogenase and enzymes in a soluble leaf proteome during freezing and drying. Biochim. Biophys. Acta: 1517-1525, doi: 0.1016/j.bbapap.2015.05.002.

  • Rillig, M.C., Rolff, J., Tietjen, B., Wehner, J. and Andrade-Linares, D. (2015). Community priming – effects of sequential stressors on microbial assemblages. FEMS Microbiol. Ecol. 91: fiv040, doi: 0.1093/femsec/fiv040.

  • Rodriguez-Rojas, A., Makarova, O., Mueller, U. and Rolff, J. (2015). Cationic peptides facilitate iron-induced mutagenesis in bacteria, PLoS Genet. 11: e1005546, doi: 10.1371/journal.pgen.1005546.

  • Schöning, C. and Wurst, S. (2015). Positive effects of root-knot nematodes (Meloidogyne incognita) on nitrogen availability do not outweigh their negative effects on fitness in Nicotiana attenuata. Plant Soil 400: 381-390, doi: 10.1007/s11104-015-2738-4.

  • Schulz, E., Tohge, T., Zuther, E., Fernie, A.R. and Hincha, D.K. (2015). Natural variation in flavonol and anthocyanin metabolism during cold acclimation in Arabidopsis thaliana 30 accessions. Plant Cell Environ. 38: 1658-1672, doi: 10.1038/srep34027.

  • Zuther, E., Juszczak, I., Lee, Y.P., Baier, M. and Hincha, D.K. (2015). Time-dependent deacclimation after cold acclimation in Arabidopsis thaliana accessions. Sci. Rep. 5: 12199, doi: 10.1038/srep12199.

2014

  • Aguilar-Trigueros, C.A., Powell, J.R., Anderson, I.C., Antonovics, J. and Rillig, M.C. (2014). Ecological understanding of root-infecting fungi using trait-based approaches. Trends Plant Sci. 19: 432-438, doi: 10.1016/j.tplants.2014.02.006.

  • Beyaert, I. and Hilker, M. (2014). Plant odour plumes as mediators of plant-insect interactions. Biol. Rev. 89: 68-81, doi: 10.1111/brv.12043.

  • Cortleven, A., Nitschke, S., Klaumünzer, M., AbdElgawad, H., Asard, H., Grimm, B., Lurz, R., Riefler, M. and Schmülling, T. (2014). A novel protective function for cytokinin in the light stress response is mediated through the AHK2 and AHK3 receptors. Plant Physiol. 164: 1470-1483, doi: 10.1104/pp.113.224667.

  • Dethloff, F., Erban, A., Orf, I., Alpers, J., Fehrle, I., Beine-Golovchuk, O., Schmidt, S., Schwachtje, J. and Kopka, J. (2014). Profiling methods to identify cold-regulated primary metabolites using gas chromatography coupled to mass spectrometry. Meth. Mol. Biol. 1166: 171-197. In: D.K. Hincha, E. Zuther (eds), Plant Cold Acclimation: Methods and Protocols, doi: 10.1007/978-1-4939-0844-8_14.

  • Dobson, A., Purves, J. and Rolff, J. (2014). Increased survival of experimentally evolved antimicrobial peptide-resistant S. aureus in an animal host. Evol. Appl. 7: 905-912, doi: 10.1111/eva.12184.

  • Hilker, M. (2014). New synthesis: Parallels between biodiversity and chemodiversity. J. Chem. Ecol. 40: 225-226, doi: doi: 10.1007/s10886-014-0402-8.

  • Hiltscher, H., Rudnik, R., Shaikhali, J., Heiber, I., Mellenthin, M., Meirelles Duarte, I., Schuster, G., Kahmann, U. and Baier, M. (2014). The radical induced cell death protein 1 (RCD1) supports transcriptional activation of genes for chloroplast antioxidant enzymes. Front. Plant Sci. 5: 475, doi: 10.3389/fpls.2014.00475.

  • Hincha, D.K. and Zuther, E. (2014). Introduction - Plant cold acclimation and freezing tolerance. In: Plant Cold Acclimation. D.K. Hincha and E. Zuther (eds.), Methods in Molecular Biology, Vol. 1166, pp. 1-6, Springer Humana Press, New York, doi: 10.1007/978-1-4939-0844-8_1.

  • Hincha, D.K. and Zuther, E. (eds.) (2014). Plant Cold Acclimation, Methods in Molecular Biology, Vol. 1166, 282 pp., Springer Humana Press, New York, doi: 10.1007/978-1-4939-0844-8.

  • Huege, J., Goetze, J., Dethloff, F., Junker, B. and Kopka, J. (2014). Quantification of stable isotope label in metabolites via mass spectrometry. Methods Mol. Biol. 1056: 213-223, doi: 10.1007/978-1-62703-592-7_20.

  • Juszczak, I. and Baier, M. (2014). Quantification of superoxide and hydrogen peroxide in leaves. In: Plant cold Acclimation. Methods and Protocols. D.K. Hincha and E. Zuther (eds.), Humana Press, pp. 217-224, doi: 10.1007/978-1-4939-0844-8_16.

  • Kabelitz, T., Kappel, C., Henneberger, K., Benke, E., Nöh, C. and Bäurle, I. (2014). eQTL Mapping of transposon silencing reveals a position-dependent stable escape from epigenetic silencing and transposition of AtMu1 in the Arabidopsis lineage. Plant Cell 26: 3261-3271, doi: 10.1105/tpc.114.128512.

  • Kafle, D., Krähmer, A., Naumann, A. and Wurst, S. (2014). Genetic variation of the host plant species matters for interactions with above- and belowground herbivores. Insects 5: 651-667, doi: 10.3390/insects5030651.

  • Kumar, P., Pandit, S.S., Steppuhn, A. and Baldwin, I.T. (2014). Natural history-driven, plant-mediated RNAi-based study reveals CYP6B46’s role in a nicotine-mediated antipredator herbivore defense. P. Natl. Acad. Sci. 111: 1245-1252, doi: 10.1073/pnas.1314848111.

  • Lassig, R., Gutermuth, T., Bey, T.D., Konrad, K.R. and Romeis, T. (2014). Pollen tube NAD(P)H oxidases act as a speed control to dampen growth rate oscillations during polarized cell growth. Plant J. 78: 94-106, doi: 10.1111/tpj.12452.

  • Lu, D., Wang, T., Persson, S., Mueller-Roeber, B. and Schippers, J.H.M. (2014). Transcriptional control of ROS homeostasis by KUODA1 regulates cell expansion during leaf development. Nat. Commun. 5: 3767, doi: 10.1038/ncomms4767.

  • Mellenthin, M., Ellersiek, U., Börger, A. and Baier, M. (2014). Expression of the Arabidopsis sigma factor SIG5 is photoreceptor and photosynthesis controlled. Plants 3: 359-391, doi: 10.3390/plants3030359.

  • Monaghan, J., Matschi, S., Romeis, T. and Zipfel, C. 2015. The calcium-dependent protein kinase CPK28 negatively regulates BIK1-mediated PAMP-induced calcium burst. Plant Signal. Behav. 10: e1018497, doi: 10.1080/15592324.2015.1018497.

  • Monaghan, J., Matschi, S., Shorinola, O., Rovenich, H., Matei, A., Segonzac, C., Malinovsky, F.G., Rathjen, J.P., MacLean, D., Romeis, T. and Zipfel, C. (2014). The calcium-dependent protein kinase CPK28 buffers plant immunity and regulates BIK1 turnover. Cell Host Microbe 16: 605-615, doi: 10.1016/j.chom.2014.10.007.

  • Reinecke, A. and Hilker, M. (2014). Plant semiochemicals – perception and behavioural responses by insects. Annu. Plant Rev. 47: 115 – 154. In: Insect – Plant Interactions. C. Voelckel and G. Jander (eds.), Wiley, doi: 10.1002/9781118829783.ch4.  

  • Rodríguez-Rojas, A., Makarova, O. and Rolff, J. (2014). Antimicrobials, stress and mutagenesis. PLoS Pathog. 10: e1004445, doi: 10.1371/journal.ppat.1004445.

  • Romeis, T. and Herde, M. (2014). From local to global: CDPKs in systemic defense signaling upon microbial and herbivore attack. Curr. Opin. Plant Biol. 20: 1-10, doi: 10.1016/j.pbi.2014.03.002.

  • Schlicke, H., Hartwig, A.S., Firtzlaff, V., Richter, A.S., Glasser, C., Maier, K., Finkemeier, I. and Grimm B. (2014). Induced deactivation of genes encoding chlorophyll biosynthesis enzymes disentangles tetrapyrrole-mediated retrograde signaling. Mol. Plant 7: 1211-1227, doi: 10.1093/mp/ssu034.

  • Seybold, H., Trempel, F., Ranf, S., Scheel, D., Romeis, T. and Lee. J. (2014). Ca2+ signalling in plant immune response: from pattern recognition receptors to Ca2+ decoding mechanisms. New Phytol. 204: 782-790, doi: 10.1111/nph.13031.

  • Stief, A., Altmann, S., Hoffmann, K., Datt Pant, B., Scheible, W.-R. and Bäurle, I.(2014). Arabidopsis miR156 regulates tolerance to recurring environmental stress through SPL transcription factors. Plant Cell 26: 1792-1807, doi: 10.1105/tpc.114.123851.

  • Stief, A., Brzezinka, K., Lämke, J. and Bäurle, I. (2014). Epigenetic responses to heat stress at different time scales and the involvement of short RNAs. Plant Signal. Behav. 9: e970430, doi: 10.4161/15592316.2014.970430.

  • Thalhammer, A., Bryant, G., Sulpice, R. and Hincha, D.K. (2014). Disordered cold regulated15 proteins protect chloroplast membranes during freezing through binding and folding, but do not stabilize chloroplast enzymes in-vivo. Plant Physiol. 166: 190-201, doi: 10.1104/pp.114.245399.

  • Thalhammer, A. and Hincha, D.K. (2014). A mechanistic model of COR15 protein function in plant freezing tolerance: integration of structural and functional characteristics. Plant Signal. Behav. 9: e977722, doi: 10.4161/15592324.2014.977722.

  • Thalhammer, A., Hincha, D.K. and Zuther, E. (2014). Measuring freezing tolerance: electrolyte leakage and chlorophyll fluorescence assays. In: Plant Cold Acclimation. D.K. Hincha and E. Zuther E (eds.), Methods in Molecular Biology, Vol. 1166, pp. 15-24, Springer Humana Press, New York, doi: 10.1007/978-1-4939-0844-8_3.

  • Weckwerth, P., Ehlert B. and Romeis, T. (2014). ZmCPK1, a calcium-independent kinase member of the Zea mays CDPK gene family, functions as a negative regulator in cold stress signalling. Plant Cell Environ. 38: 544-58, doi: 10.1111/pce.12414.

2013

  • Duan, G., Christian, N., Schwachtje, J., Walther, D. and Ebenhöh, O. (2013). The metabolic interplay between plants and phytopathogens. Metabolites 3: 1-23, doi: 10.3390/metabo3010001.

  • Dubiella, U., Seybold, H., Durian, G., Komander, E., Lassig, R., Witte, C-P., Schulze W.X. and Romeis, T. (2013). Calcium-dependent protein kinase/NADPH oxidase activation circuit is required for rapid defense signal propagation. Proc. Natl. Acad. Sci. USA. 110: 8744-8749, doi: 10.1073/pnas.1221294110.

  • Dunn, W. B., Erban, A., Weber, R. J. M., Creek, D. J., Brown, M., Breitling, R., Hankemeier, T., Goodacre, R., Neumann, S., Kopka, J. and Viant, M. R. (2013). Mass appeal: metabolite identification in mass spectrometry-focused untargeted metabolomics. Metabolomics 9: S44-S66, doi: 10.1007/s11306-012-0434-4.

  • Gechev, T.S., Benina, M., Obata, T., Tohge, T., Sujeeth, N., Minkov, I., Hille, J., Temanni, M.R., Marriott, A.S., Bergström, E., Thomas-Oates, J., Antonio, C., Mueller-Roeber, B., Schippers, J.H., Fernie, A.R. and Toneva, V. (2013). Molecular mechanisms of desiccation tolerance in the resurrection glacial relic Haberlea rhodopensis. Cell Mol. Life Sci. 70: 689-709, doi: 10.1007/s00018-012-1155-6.

  • Geiselhardt, S., Yoneya, K., Blenn, B., Drechsler, N., Gershenzon, J., Kunze, R. and Hilker, M. (2013). Egg laying of cabbage white butterfly (Pieris brassicae) on Arabidopsis thaliana affects subsequent performance of the larvae. PLoS ONE 8: e59661, doi: 10.1371/journal.pone.0059661.

  • Heiber, I., Wenguo, C. and Baier, M. (2013). Linking chloroplast antioxidant defence to carbohydrate availability: The transcript abundance of stromal ascorbate peroxidase is sugar controlled via ascorbate. Mol. Plant 7: 58-70, doi: 10.1093/mp/sst154.

  • Lee, Y.P., Giorgi, F.M., Lohse, M., Kvederaviciute, K., Klages, S., Usadel, B., Meskiene, I., Reinhardt, R. and Hincha, D.K. (2013). Transcriptome sequencing and microarray design for functional genomics in the extremophile Arabidopsis relative Thellungiella salsuginea (Eutrema salsugineum). BMC Genomics 14: 793, doi: 10.1186/1471-2164-14-793.

  • Meissner, M., Orsini, E., Ruschhaupt, M., Melchinger, A.E., Hincha, D.K. and Heyer, A.G. (2013). Mapping quantitative trait loci for freezing tolerance in a recombinant inbred line population of Arabidopsis thaliana accessions Tenela and C24 reveals REVEILLE1 as negative regulator of cold acclimation. Plant Cell Environ. 36: 1256-1267, doi: 10.1111/pce.12054.

  • Scarpeci, T.E., Zanor, M.I., Mueller-Roeber, B. and Valle, E.M. (2013). Overexpression of AtWRKY30 enhances abiotic stress tolerance during early growth stages in Arabidopsis thaliana. Plant Mol. Biol. 3: 265-77, doi: 10.1007/s11103-013-0090-8.

  • Schmidt, M., Mieulet. D., Hubberten, H.-M., Obata, T., Hoefgen. R., Fernie, A.R., Fisahn, J., San Segundo, B., Guiderdoni, B., Schippers, J.H. and Mueller-Roeber, B. (2013). SALT-RESPONSIVE ERF1 regulates ROS-dependent signalling during the initial response to salt stress in rice. Plant Cell 6: 2115-31, doi: 10.1105/tpc.113.113068.

  • Strehmel, N., Kopka, J., Scheel, D. and Böttcher, C. (2013). Annotating unknown components from GC/EI-MS-based metabolite profiling experiments using GC/APCI(+)-QTOFMS. Metabolomics 10: 324-336, doi: 10.1007/s11306-013-0569-y.

  • Thalhammer, A. and Hincha, D.K. (2013). The function and evolution of closely related COR/LEA (Cold-Regulated/Late Embryogenesis Abundant) proteins in Arabidopsis thaliana. Plant and Microbe Adaptations to Cold in a Changing World, pp. 89-105, doi: 10.1007/978-1-4614-8253-6_8.

  • Ullrich Dubiella, U., Seybold, H., Durian, G., Komander, E., Lassig, R., Witte, C.-P., Schulze W.X. and Romeis, T. (2013). Calcium-dependent protein kinase/NADPH oxidase activation circuit is required for rapid defense signal propagation. P. Natl. Acad. Sci. 110: 8744-8749, doi: 10.1073/pnas.1221294110.

  • Wurst, S. (2013). Plant-mediated links between detritivores and aboveground herbivores. Front. Plant Sci. 4: 380, doi: 10.3389/fpls.2013.00380.

2012

  • Balazadeh, S., Jaspert, N., Arif, M., Mueller-Roeber, B. and Maurino V.G. (2012). Expression of ROS-responsive genes and transcription factors after metabolic formation of H2O2 in chloroplasts. Front. Plant Sci. 3: 234, doi: 10.3389/fpls.2012.00234.

  • Beyaert, I., Köpke, D., Stiller, J., Hammerbacher, A., Yoneya, K., Schmidt, A., Gershenzon, J. and Hilker, M. (2012). Can insect egg deposition “warn“ a plant of future feeding damage by herbivorous larvae? Proc. Roy. Soc. London, Ser. B 279: 101–108, doi: 10.1098/rspb.2011.0468.

  • Brenner, W.G., Ramireddy, E., Heyl, A. and Schmülling, T. (2012). Gene regulation by cytokinin in Arabidopsis. Front. Plant. Sci. 3: 8, doi: 10.3389/fpls.2012.00008.

  • Brenner, W.G. and Schmülling, T. (2012). Transcript profiling of cytokinin action in Arabidopsis roots and shoots discovers largely similar but also organ-specific responses. BMC Plant Biol.12: 112, doi: 10.1186/1471-2229-12-112.

  • Degenkolbe, T., Giavalisco, P., Zuther, E., Seiwert, B., Hincha, D.K. and Willmitzer, L. (2012). Differential remodeling of the lipidome during cold acclimation in natural accessions of Arabidopsis thaliana. Plant J. 72: 972-982, doi: 10.1111/tpj.12007.

  • Juszczak, I. and Baier, M. (2012). The strength of the miR398-Csd2-CCS1 regulon is subject to natural variation in Arabidopsis thaliana. FEBS Lett. 586: 3385-3390, doi: 10.1016/j.febslet.2012.07.049.

  • Juszczak, I., Rudnik, R., Pietzenuk, B. and Baier, M. (2012). Natural genetic variation in the expression regulation of the chloroplast antioxidant system among Arabidopsis thaliana accessions. Physiol. Plant. 146: 53-70, doi: 10.1111/j.1399-3054.2012.01602.x.

  • Lai, A.G., Doherty, C.J., Mueller-Roeber, B., Kay, S.A., Schippers, J.H. and Dijkwel, P.P. (2012). CIRCADIAN CLOCK-ASSOCIATED 1 regulates ROS homeostasis and oxidative stress responses. Proc. Natl. Acad. Sci. USA 109: 17129-17134, doi: 10.1073/pnas.1209148109.

  • Lee, Y.P., Babakov, A., de Boer, B., Zuther, E. and Hincha, D.K. (2012). Comparison of freezing tolerance, compatible solutes and polyamines in geographically diverse collections of Thellungiella sp. and Arabidopsis thaliana accessions. BMC Plant Biol.12: 131, doi: 10.1186/1471-2229-12-131.

  • Schippers, J.H., Nguyen, H.M., Lu, D., Schmidt R. and Mueller-Roeber B. (2012). ROS homeostasis during development: an evolutionary conserved strategy. Cell Mol. Life Sci. 69: 3245-3257, doi: 10.1007/s00018-012-1092-4.

  • Shahnejat-Bushehri, S., Balazadeh, S. and Mueller-Roeber B.(2012). Arabidopsis NAC transcription factor JUNGBRUNNEN1 affects thermomemory-associated genes and enhances heat stress tolerance in primed and unprimed conditions. Plant Signal. Behav. 7: 1518–1521, doi: 10.4161/psb.22092.

  • Zuther, E., Schulz, E., Childs, L.H. and Hincha, D.K. (2012). Clinal variation in the non-acclimated and cold-acclimated freezing tolerance of Arabidopsis thaliana accessions. Plant Cell Environ. 35: 1860-1878, doi: 10.1111/j.1365-3040.2012.02522.x.