References
- Cove D. The moss physcomitrella patens. Annu Rev Genet. 2005;39(1):339–6. doi:10.1146/annurev.genet.39.073003.110214. PMID: 16285864
- Falz AL, Müller-Schüssele SJ. Physcomitrella as a model system for plant cell biology and organelle-organelle communication. Curr Opin Plant Biol. 2019;52:7–13. PMID:31254720. doi:10.1016/j.pbi.2019.05.007.
- Rensing SA, Goffinet B, Meyberg R, Wu SZ, Bezanilla M. The moss Physcomitrium (Physcomitrella) patens: a model organism for non-seed plants. Plant Cell. 2020;32(5):1361–1376. doi:10.1105/tpc.19.00828. PMID:32152187
- Rensing SA, Lang D, Zimmer AD, Terry A, Salamov A, Shapiro H, Nishiyama T, Perroud P-F, Lindquist EA, Kamisugi Y, et al. The Physcomitrella genome reveals evolutionary insights into the conquest of land by plants. Science. 2008;319(5859):64–69. PMID:18079367. doi:10.1126/science.1150646.
- Kudla J, Becker D, Grill E, Hedrich R, Hippler M, Kummer U, Parniske M, Romeis T, Schumacher K. Advances and current challenges in calcium signaling. New Phytol. 2018;218(2):414–431. doi:10.1111/nph.14966. PMID:29332310
- Tian W, Wang C, Gao QF, Li LG, Luan S. Calcium spikes, waves and oscillations in plant development and biotic interactions. Nat Plants. 2020;6(7):750–759. doi:10.1038/s41477-020-0667-6. PMID:32601423
- Demidchik V, Shabala S, Isayenkov S, Cuin TA, Pottosin I. Calcium transport across plant membranes: mechanisms and functions. New Phytol. 2018;220(1):49–69. doi:10.1111/nph.15266. PMID:29916203
- Lam HM, Chiu J, Hsieh MH, Meisel L, Oliveira IC, Shin M, Coruzzi G. Glutamate-receptor genes in plants. Nature. 1998;396(6707):125–126. doi:10.1038/24066. PMID:9823891
- Leng Q, Mercier RW, Yao W, Berkowitz GA. Cloning and first functional characterization of a plant cyclic nucleotide-gated cation channel. Plant Physiol. 1999;121(3):753–761. doi:10.1104/pp.121.3.753. PMID:10557223
- Hou CC, Tian W, Kleist T, He K, Garcia V, Bai FL, Hao YL, Luan S, Li LG. DUF221 proteins are a family of osmosensitive calcium-permeable cation channels conserved across eukaryotes. Cell Res. 2014;24(5):632–635. doi:10.1038/cr.2014.14. PMID: 24503647
- Yuan F, Yang HM, Xue Y, Kong DD, Ye R, Li CJ, Zhang J, Theprungsirikul L, Shrift T, Krichilsky B, et al. OSCA1 mediates osmotic-stress-evoked Ca2+ increases vital for osmosensing in Arabidopsis. Nature. 2014;514(7522):367–371. doi:10.1038/nature13593. PMID: 25162526
- Frachisse JM, Thomine S, Allain JM. Calcium and plasma membrane force-gated ion channels behind development. Curr Opin Plant Biol. 2020;53:57–64. PMID:31783322. doi:10.1016/j.pbi.2019.10.006.
- Jarratt-Barnham E, Wang L, Ning Y, Davies JM. The complex story of plant cyclic nucleotide-gated channels. Int J Mol Sci. 2021;22(2):874. doi:10.3390/ijms22020874. PMID:33467208
- Ortiz-Ramírez C, Michard E, Simon AA, Damineli DSC, Hernández-Coronado M, Becker JD, Feijó JA. GLUTAMATE RECEPTOR-LIKE channels are essential for chemotaxis and reproduction in mosses. Nature. 2017;549(7670):91–95. doi:10.1038/nature23478. PMID:28737761
- Kang J, Turano FJ. The putative glutamate receptor 1.1 (AtGLR1.1) functions as a regulator of carbon and nitrogen metabolism in Arabidopsis thaliana. Proc Natl Acad Sci USA. 2003;100(11):6872–6877. doi:10.1073/pnas.1030961100. PMID:12738881
- Cho D, Kim SA, Murata Y, Lee S, Jae SK, Nam HG, Kwak JM. De-regulated expression of the plant glutamate receptor homolog AtGLR3.1 impairs long-term Ca 2+-programmed stomatal closure. Plant J. 2009;58(3):437–449. doi:10.1111/j.1365-313X.2009.03789.x. PMID:19143998
- Michard E, Lima PT, Borges F, Silva AC, Portes MT, Carvalho JE, Gilliham M, Liu L-H, Obermeyer G, Feijó JA, et al. Glutamate receptor–like genes form Ca 2+channels in pollen tubes and are regulated by pistil d-serine. Science. 2011;332(6028):434–437. PMID:21415319. doi:10.1126/science.1201101.
- Vincill ED, Clarin AE, Molenda JN, Spalding EP. Interacting glutamate receptor-like proteins in phloem regulate lateral root initiation in Arabidopsis. Plant Cell. 2013;25(4):1304–1313. doi:10.1105/tpc.113.110668. PMID:23590882
- Kong D, Ju C, Parihar A, Kim S, Cho D, Kwak JM. Arabidopsis glutamate receptor homolog AtGLR3.5 modulates cytosolic Ca2+ level to counteract effect of abscisic acid in seed germination. Plant Physiol. 2015;167(4):1630–1642. doi:10.1104/pp.114.251298. PMID:25681329
- Kong D, Hu H-C, Okuma E, Lee Y, Lee HS, Munemasa S, Cho D, Ju C, Pedoeim L, Rodriguez B, Wang J, Im W, Murata Y, Pei ZM, Kwak JM. L-Met activates Arabidopsis GLR Ca2+ channels upstream of ROS production and regulates stomatal movement. Cell Rep. 2016;17(10):2553–2561. PMID:27926860. doi:10.1016/j.celrep.2016.11.015.
- Wudick MM, Portes MT, Michard E, Rosas-Santiago P, Lizzio MA, Nunes CO, Campos C, Santa Cruz Damineli D, Carvalho JC, Lima PT, et al. CORNICHON sorting and regulation of GLR channels underlie pollen tube Ca 2+homeostasis. Science. 2018;360(6388):533–536. PMID:29724955. doi:10.1126/science.aar6464.
- Meyerhoff O, Muller K, Roelfsema MRG, Latz A, Lacombe B, Hedrich R, Dietrich P, Becker D. AtGLR3.4, a glutamate receptor channel-like gene is sensitive to touch and cold. Planta. 2005;222(3):418–427. doi:10.1007/s00425-005-1551-3. PMID:15864638
- Li F, Wang J, Ma CL, Zhao YX, Wang YC, Hasi A, Qi Z. Glutamate receptor-like channel3.3 is involved in mediating glutathione-triggered cytosolic calcium transients, transcriptional changes, and innate immunity responses in Arabidopsis. Plant Physiol. 2013;162(3):1497–1509. doi:10.1104/pp.113.217208. PMID:23656893
- Mousavi SAR, Chauvin A, Pascaud F, Kellenberger S, Farmer EE. GLUTAMATE RECEPTOR-LIKE genes mediate leaf-to-leaf wound signaling. Nature. 2013;500(7463):422–426. doi:10.1038/nature12478. PMID:23969459
- Toyota M, Spencer D, Sawai-Toyota S, Jiaqi W, Zhang T, Koo AJ, Howe GA, Gilroy S. Glutamate triggers long-distance, calcium-based plant defense signaling. Science. 2018;361(6407):1112–1115. doi:10.1126/science.aat7744. PMID:30213912
- Li M, Wang F, Li S, Yu G, Wang L, Li Q, Zhu X, Li Z, Yuan L, Liu P. Importers drive leaf-to-leaf jasmonic acid transmission in wound-induced systemic immunity. Mol Plants. 2020;13(10):1485–1498. PMID:32889174. 10.1016/j.molp.2020.08.017.
- Chen L, Bao F, Tang S, Zuo E, Lv Q, Zhang D, Hu Y, Wang X, He Y. PpAKR1A, a novel Aldo-Keto reductase from Physcomitrella patens, plays a positive role in salt stress. Int J Mol Sci. 2019;20(22):5723. doi:10.3390/ijms20225723. PMID: 31739643
- Jefferson RA, Kavanagh TA, Bevan MW. GUS fusions: b-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 1987;6(13):3901–3907. doi:10.1002/j.1460-2075.1987.tb02730.x. PMID: 3327686
- Forde BG, Roberts MR. Glutamate receptor-like channels in plants: a role as amino acid sensors in plant defence? F1000Prime Rep. 2014;6:37. PMID:24991414. doi:10.12703/P6-37.
- Wudick MM, Michard E, Oliveira C, Feijó JA. Comparing plant and animal glutamate receptors: common traits but different fates? J Exp Bot. 2018;17(17):4151–4163. doi:10.1093/jxb/ery153. PMID:29684179
- Cheng Y, Zhang X, Sun T, Tian Q, Zhang WH. Glutamate receptor homolog3.4 is involved in regulation of seed germination under salt stress in Arabidopsis. Plant & Cell Physiol. 2018;59(5):978–988. doi:10.1093/pcp/pcy034. PMID:29432559
- Chen PY, Hsu CY, Lee CE, Chang IF. Arabidopsis glutamate receptor GLR3.7 is involved in abscisic acid response. Plant Signal Behav. 2021;12(12):1997513. doi:10.1080/15592324.2021.1997513. PMID:34763610
- De Bortoli S, Teardo E, Szabò I, Morosinotto T, Alboresi A. Evolutionary insight into the ionotropic glutamate receptor superfamily of photosynthetic organisms. Biophys Chem. 2016;218:14–26. PMID:27586818. doi:10.1016/j.bpc.2016.07.004.