SRF3-bHLH Crosstalk in Arabidopsis Iron Homeostasis: Receptor Kinase Signaling, Transcriptional Regulation and Genetic Epistasis

Authors

  • Zain Haider Department of Plant pathology, University of Agriculture, Faisalabad, Pakistan
  • Sadia Farah Imran Albrecht Daniel Thaer-Institute of Agricultural and Horticultural Sciences, Humboldt-Universität zu Berlin, Germany
  • Ali Raza Department of Botany, University of Agriculture Faisalabad, Pakistan.
  • Abdul Latif Universidade Federal de Pelotas (UFPel), Brazil
  • Maryam Saleem
  • Muhammad Amir Virology lab, Centre of Agricultural Biochemistry and Biotechnology, University of Agriculture Faisalabad, Pakistan

DOI:

https://doi.org/10.38211/joarps.2026.07.368

Keywords:

Iron homeostasis; bHLH transcription factors; SRF3; receptor kinase signaling; genetic epistasis; plant immunity

Abstract

In this review, the available evidence that connects the SRF3 receptor kinase with the bHLH-driven Fe-deficiency regulatory network in Arabidopsis plants is summarized. The data currently available suggests that SRF3 and bHLH-mediated regulation are functionally convergent in the regulation of IRT1, but there is currently no evidence for direct genetic epistasis or physical interaction between these regulators. Three possible models are considered: SRF3 could act upstream of bHLH regulators; SRF3 could be active alongside the bHLH pathway; or SRF3 could have indirect effects on bHLH activity such as by phosphorylation, protein stability or subcellular localization. Based on these models, genetic interaction experiments between SRF3 and important bHLH mutants, as well as transcriptional, protein-level and phosphoproteomic experiments, are suggested to determine the pathway hierarchy and molecular connectivity. Further research is also needed to uncover the role of SRF3–bHLH crosstalk in coordinating iron homeostasis with plant immunity and how insights can be used to develop strategies for enhancing iron acquisition and nutritional quality in crops. Overall, the SRF3-bHLH relationship is a hypothesis to be tested, not a pathway

63 25

Downloads

Download data is not yet available.

References

Angeles-Albores, D., Puckett Robinson, C., Williams, B. A., Wold, B. J., & Sternberg, P. W. (2018). Reconstructing a metazoan genetic pathway with transcriptome-wide epistasis measurements. Proceedings of the National Academy of Sciences, 115(13), E2930-E2939. https://doi.org/doi:10.1073/pnas.1712387115 DOI: https://doi.org/10.1073/pnas.1712387115

Azam, H., Pierro, L., Reina, M., Gallagher, W. M., & Prencipe, M. (2022). Emerging role for the Serum Response Factor (SRF) as a potential therapeutic target in cancer. Expert Opinion on Therapeutic Targets, 26(2), 155-169. DOI: https://doi.org/10.1080/14728222.2022.2032652

Baby, D., Weldi, S., Knopf, M., Venkadasamy, V., Erickson, J. L., & Bauer, P. (2025). A three amino acid sequence gates protein stability control of bHLH104 and iron uptake in Arabidopsis thaliana. Plant, Cell & Environment. DOI: https://doi.org/10.1101/2025.11.18.689088

Bais, P., Alidrissi, L., & Blilou, I. (2023). Detecting Protein-Protein Interactions Using Bimolecular Fluorescence Complementation (BiFC) and Luciferase Complementation Assays (LCA). Methods Mol Biol, 2690, 121-131. https://doi.org/10.1007/978-1-0716-3327-4_12 DOI: https://doi.org/10.1007/978-1-0716-3327-4_12

Berger, N., Marin, A. J., Stassen, M., Lourenço, T., Li, M., Watanabe, S., & Marino, D. (2024). Molecular Regulation of Iron Homeostasis. Progress in Botany, 85, 75. DOI: https://doi.org/10.1007/124_2023_76

Berger, N., Marin, A. J., Stassen, M. J., Lourenço, T., Li, M., Watanabe, S.,…Marino, D. (2023). Molecular regulation of iron homeostasis in plants. In Progress in Botany Vol. 85 (pp. 75-103). Springer. DOI: https://doi.org/10.1007/124_2023_76

Bhat, M. A., Mishra, A. K., Shah, S. N., Bhat, M. A., Jan, S., Rahman, S.,…Jan, A. T. (2024). Soil and mineral nutrients in plant health: A prospective study of iron and phosphorus in the growth and development of plants. Current Issues in Molecular Biology, 46(6), 5194-5222. DOI: https://doi.org/10.3390/cimb46060312

Cai, Y., Li, Y., & Liang, G. (2021). FIT and bHLH Ib transcription factors modulate iron and copper crosstalk in Arabidopsis. Plant, Cell & Environment, 44(5), 1679-1691. https://doi.org/https://doi.org/10.1111/pce.14000 DOI: https://doi.org/10.1111/pce.14000

Cappellari, O. (2012). Endothelial-derived Dll4 and PDGF-BB reprogram committed skeletal myoblasts to a pericytes fate without erasing their myogenic memory. DOI: https://doi.org/10.1016/j.devcel.2013.01.022

Chia, J.-C., & Vatamaniuk, O. (2024). Shall we talk? New details in crosstalk between copper and iron homeostasis uncovered in Arabidopsis thaliana. New Phytologist, 242. https://doi.org/10.1111/nph.19583 DOI: https://doi.org/10.1111/nph.19583

Choi, S. G., Richardson, A., Lambourne, L., Hill, D. E., & Vidal, M. (2018). Protein Interactomics by Two-Hybrid Methods. Methods Mol Biol, 1794, 1-14. https://doi.org/10.1007/978-1-4939-7871-7_1 DOI: https://doi.org/10.1007/978-1-4939-7871-7_1

de Martin, X., Sodaei, R., & Santpere, G. (2021). Mechanisms of binding specificity among bHLH transcription factors. International Journal of Molecular Sciences, 22(17), 9150. DOI: https://doi.org/10.3390/ijms22179150

De Storme, N., & Geelen, D. (2014). Callose homeostasis at plasmodesmata: molecular regulators and developmental relevance. Frontiers in Plant Science, 5, 138. DOI: https://doi.org/10.3389/fpls.2014.00138

Ding, W., Yu, Z., Tong, Y., Huang, W., Chen, H., & Wu, P. (2009). A transcription factor with a bHLH domain regulates root hair development in rice. Cell research, 19, 1309-1311. https://doi.org/10.1038/cr.2009.109 DOI: https://doi.org/10.1038/cr.2009.109

Duan, Y., Wang, Z., Fang, Y., Pei, Z., Hu, H., Xu, Q.,…Chen, X. (2024). A secreted fungal laccase targets the receptor kinase OsSRF3 to inhibit OsBAK1–OsSRF3-mediated immunity in rice. Nature communications, 15(1), 7891. https://doi.org/10.1038/s41467-024-52204-w DOI: https://doi.org/10.1038/s41467-024-52204-w

Escocard de Azevedo Manhães, A. M., Ortiz‐Morea, F. A., He, P., & Shan, L. (2021). Plant plasma membrane‐resident receptors: Surveillance for infections and coordination for growth and development. Journal of integrative plant biology, 63(1), 79-101. DOI: https://doi.org/10.1111/jipb.13051

Gao, F., & Dubos, C. (2021). Transcriptional integration of plant responses to iron availability. Journal of experimental botany, 72(6), 2056-2070. DOI: https://doi.org/10.1093/jxb/eraa556

Gao, F., & Dubos, C. (2024). The arabidopsis bHLH transcription factor family. Trends in plant science, 29(6), 668-680. DOI: https://doi.org/10.1016/j.tplants.2023.11.022

Gao, F., Li, M., & Dubos, C. (2024). bHLH121 and clade IVc bHLH transcription factors synergistically function to regulate iron homeostasis in Arabidopsis thaliana. J Exp Bot, 75(10), 2933-2950. https://doi.org/10.1093/jxb/erae072 DOI: https://doi.org/10.1093/jxb/erae072

Gao, F., Robe, K., Gaymard, F., Izquierdo, E., & Dubos, C. (2019). The transcriptional control of iron homeostasis in plants: a tale of bHLH transcription factors? Frontiers in Plant Science, 10, 6. DOI: https://doi.org/10.3389/fpls.2019.00006

Gratz, R., Manishankar, P., Ivanov, R., Köster, P., Mohr, I., Trofimov, K.,…Brumbarova, T. (2019). CIPK11-Dependent Phosphorylation Modulates FIT Activity to Promote Arabidopsis Iron Acquisition in Response to Calcium Signaling. Developmental Cell, 48(5), 726-740.e710. https://doi.org/https://doi.org/10.1016/j.devcel.2019.01.006 DOI: https://doi.org/10.1016/j.devcel.2019.01.006

Hao, Y., Zong, X., Ren, P., Qian, Y., & Fu, A. (2021). Basic helix-loop-helix (bHLH) transcription factors regulate a wide range of functions in Arabidopsis. International Journal of Molecular Sciences, 22(13), 7152. DOI: https://doi.org/10.3390/ijms22137152

Herlihy, J. H., Long, T. A., & McDowell, J. M. (2020). Iron homeostasis and plant immune responses: recent insights and translational implications. Journal of Biological Chemistry, 295(39), 13444-13457. DOI: https://doi.org/10.1074/jbc.REV120.010856

Huang, F., Sun, M., Yao, Z., Zhou, J., Bai, Q., Chen, X.,…Shen, Y. (2024). Protein kinase SnRK2.6 phosphorylates transcription factor bHLH3 to regulate anthocyanin homeostasis during strawberry fruit ripening. Journal of experimental botany, 75(18), 5627-5640. https://doi.org/10.1093/jxb/erae250 DOI: https://doi.org/10.1093/jxb/erae250

Jiang, M., Wu, S., Xie, K., Zhou, G., Zhou, W., & Bao, P. (2024). The significance of ferroptosis in renal diseases and its therapeutic potential. Heliyon, 10(16). DOI: https://doi.org/10.1016/j.heliyon.2024.e35882

Kim, S. A., LaCroix, I. S., Gerber, S. A., & Guerinot, M. L. (2019). The iron deficiency response in Arabidopsis thaliana requires the phosphorylated transcription factor URI. Proceedings of the National Academy of Sciences, 116(50), 24933-24942. DOI: https://doi.org/10.1073/pnas.1916892116

Kim, S. A., LaCroix, I. S., Gerber, S. A., & Guerinot, M. L. (2019). The iron deficiency response in Arabidopsis thaliana requires the phosphorylated transcription factor URI. Proc Natl Acad Sci U S A, 116(50), 24933-24942. https://doi.org/10.1073/pnas.1916892116 DOI: https://doi.org/10.1073/pnas.1916892116

Knez, M., Graham, R. D., Welch, R. M., & Stangoulis, J. C. (2017). New perspectives on the regulation of iron absorption via cellular zinc concentrations in humans. Critical Reviews in Food Science and Nutrition, 57(10), 2128-2143. DOI: https://doi.org/10.1080/10408398.2015.1050483

Kumar, A., Kaur, G., Singh, P., Meena, V., Sharma, S., Tiwari, M.,…Pandey, A. K. (2022). Strategies and bottlenecks in hexaploid wheat to mobilize soil iron to grains. Frontiers in Plant Science, 13, 863849. DOI: https://doi.org/10.3389/fpls.2022.863849

Lei, R., Li, Y., Cai, Y., Li, C., Pu, M., Lu, C.,…Liang, G. (2020). bHLH121 functions as a direct link that facilitates the activation of FIT by bHLH IVc transcription factors for maintaining Fe homeostasis in Arabidopsis. Molecular Plant, 13(4), 634-649. DOI: https://doi.org/10.1016/j.molp.2020.01.006

Li, R., Ma, L., Li, M., Zhu, X., Zhai, Y., Liu, J.,…Yang, L. (2026). Iron need attention: a review on the role of iron in plants. Frontiers in Plant Science, 17, 1876801. DOI: https://doi.org/10.3389/fpls.2026.1876801

Li, W., Han, X., & Lan, P. (2022). Emerging roles of protein phosphorylation in plant iron homeostasis. Trends in plant science, 27(9), 908-921. DOI: https://doi.org/10.1016/j.tplants.2022.03.012

Li, X., Zhang, H., Ai, Q., Liang, G., & Yu, D. (2016). Two bHLH Transcription Factors, bHLH34 and bHLH104, Regulate Iron Homeostasis in Arabidopsis thaliana. Plant Physiol, 170(4), 2478-2493. https://doi.org/10.1104/pp.15.01827 DOI: https://doi.org/10.1104/pp.15.01827

Liang, G. (2022). Iron uptake, signaling, and sensing in plants. Plant Communications, 3(5). DOI: https://doi.org/10.1016/j.xplc.2022.100349

Lurthy, T., Pivato, B., Lemanceau, P., & Mazurier, S. (2021). Importance of the rhizosphere microbiota in iron biofortification of plants. Frontiers in Plant Science, 12, 744445. DOI: https://doi.org/10.3389/fpls.2021.744445

Maier, S. A., Galellis, J. R., & McDermid, H. E. (2005). Phylogenetic analysis reveals a novel protein family closely related to adenosine deaminase. Journal of molecular evolution, 61(6), 776-794. DOI: https://doi.org/10.1007/s00239-005-0046-y

Mankotia, S., Singh, D., Monika, K., Kalra, M., Meena, H., Meena, V.,…Satbhai, S. B. (2023). ELONGATED HYPOCOTYL 5 regulates BRUTUS and affects iron acquisition and homeostasis in Arabidopsis thaliana. The Plant Journal, 114(6), 1267-1284. DOI: https://doi.org/10.1111/tpj.16191

Maurer, F., Naranjo Arcos, M. A., & Bauer, P. (2014). Responses of a triple mutant defective in three iron deficiency-induced basic helix-loop-helix genes of the subgroup Ib (2) to iron deficiency and salicylic acid. PLoS One, 9(6), e99234. DOI: https://doi.org/10.1371/journal.pone.0099234

McInturf, S. A. (2018). Iron Homeostasis is Hierarchically Regulated by Multiple Inputs: Evidence for the Role of Reactive Oxygen Species and Iron-zinc Cross Talk University of Missouri--Columbia].

Molnár, Z., Solomon, W., Mutum, L., & Janda, T. (2023). Understanding the mechanisms of Fe deficiency in the rhizosphere to promote plant resilience. Plants, 12(10), 1945. DOI: https://doi.org/10.3390/plants12101945

Pan, L., Huang, C., Li, R., & Li, Y. (2024). The bHLH Transcription Factor PhbHLH121 Regulates Response to Iron Deficiency in Petunia hybrida. Plants, 13(23), 3429. DOI: https://doi.org/10.3390/plants13233429

Pfister, K. (2008). Functional analysis of the STRUBBELIG-RECEPTOR FAMILY in Arabidopsis thaliana Technische Universität München].

Pireyre, M., & Burow, M. (2015). Regulation of MYB and bHLH Transcription Factors: A Glance at the Protein Level. Molecular Plant, 8(3), 378-388. https://doi.org/10.1016/j.molp.2014.11.022 DOI: https://doi.org/10.1016/j.molp.2014.11.022

Platre, M., Satbhai, S., Brent, L., Gleason, M., Cao, M., Grison, M.,…Busch, W. (2022). The receptor kinase SRF3 coordinates iron-level and flagellin dependent defense and growth responses in plants. Nature communications, 13. https://doi.org/10.1038/s41467-022-32167-6

Platre, M. P., Satbhai, S. B., Brent, L., Gleason, M. F., Cao, M., Grison, M.,…Goeschl, C. (2022). The receptor kinase SRF3 coordinates iron-level and flagellin dependent defense and growth responses in plants. Nature communications, 13(1), 4445.

Platre, M. P., Satbhai, S. B., Brent, L., Gleason, M. F., Cao, M., Grison, M.,…Busch, W. (2022). The receptor kinase SRF3 coordinates iron-level and flagellin dependent defense and growth responses in plants. Nature communications, 13(1), 4445. https://doi.org/10.1038/s41467-022-32167-6 DOI: https://doi.org/10.1038/s41467-022-32167-6

Platre, M. P., Satbhai, S. B., Brent, L., Gleason, M. F., Cao, M., Grison, M.,…Busch, W. (2022). The receptor kinase SRF3 coordinates iron-level and flagellin dependent defense and growth responses in plants. Nat Commun, 13(1), 4445. https://doi.org/10.1038/s41467-022-32167-6 DOI: https://doi.org/10.1038/s41467-022-32167-6

Qian, Y., Zhang, T., Yu, Y., Gou, L., Yang, J., Xu, J., & Pi, E. (2021). Regulatory Mechanisms of bHLH Transcription Factors in Plant Adaptive Responses to Various Abiotic Stresses [Review]. Frontiers in Plant Science, Volume 12 - 2021. https://doi.org/10.3389/fpls.2021.677611 DOI: https://doi.org/10.3389/fpls.2021.677611

Radani, Y., Li, R., Korboe, H. M., Ma, H., & Yang, L. (2023). Transcriptional and Post-Translational Regulation of Plant bHLH Transcription Factors during the Response to Environmental Stresses. Plants (Basel), 12(11). https://doi.org/10.3390/plants12112113 DOI: https://doi.org/10.3390/plants12112113

Rav, B. R., & Satbhai, S. B. (2026). Iron Deficiency Reprograms Lateral Root Growth via TAR2-Dependent Auxin Biosynthesis in Arabidopsis. Physiologia plantarum, 178(2), e70828. https://doi.org/https://doi.org/10.1111/ppl.70828 DOI: https://doi.org/10.1111/ppl.70828

Receptor-Like Kinase–membrane-anchored, R. (2021). SRF3 STRUBBELIG RECEPTOR FAMILY 3–atypical receptor kinase localized at PD and PD vesicles SUB STRUBBELIG–RLK involved in non-cell-autonomous developmental signaling via PD. Pathogen effectors, plasmodesmata, and novel vesicular structures in plant immunity.

Riaz, N., & Guerinot, M. (2021). All together now: regulation of the iron deficiency response. Journal of experimental botany, 72, 2045-2055. https://doi.org/10.1093/jxb/erab003 DOI: https://doi.org/10.1093/jxb/erab003

Robe, K., Stassen, M. J., Watanabe, S., Espadas, J., Gonzalez, P., Rossille, A.,…Santoni, V. (2025). Coumarin-facilitated iron transport: An IRT1-independent strategy for iron acquisition in Arabidopsis thaliana. Plant Communications, 6(9). DOI: https://doi.org/10.1016/j.xplc.2025.101431

Ryu, H., Choi, S., Cheng, M., Koo, B.-K., Kim, E. Y., Lee, H.-S., & Lee, D.-H. (2025). Flagellin sensing, signaling, and immune responses in plants. Plant Communications. DOI: https://doi.org/10.1016/j.xplc.2025.101383

Schwarz, B., & Bauer, P. (2020). FIT, a regulatory hub for iron deficiency and stress signaling in roots, and FIT-dependent and-independent gene signatures. Journal of experimental botany, 71(5), 1694-1705. DOI: https://doi.org/10.1093/jxb/eraa012

Schwarz, B., & Bauer, P. (2020). FIT, a regulatory hub for iron deficiency and stress signaling in roots, and FIT-dependent and -independent gene signatures. J Exp Bot, 71(5), 1694-1705. https://doi.org/10.1093/jxb/eraa012 DOI: https://doi.org/10.1093/jxb/eraa012

Shafi, Z., Shahid, M., Ilyas, T., & Singh, K. (2025). Next-generation perspectives on microbially synthesized siderophores: molecular engineering, multi-omics insights, and applications for smart climate-resilient crops. World Journal of Microbiology and Biotechnology, 41(10), 393. DOI: https://doi.org/10.1007/s11274-025-04575-5

Shi, W., Bilstein-Schloemer, M., Stolze, S., Platre, M., Hofmann, M., Doehlemann, G.,…Saur, I. (2026). Targeting of the barley cell-surface receptor SRF3 by the Blumeria hordei effector AVR A13 overlaps with AVR A13 recognition by MLA and the induction of NLR-mediated cell death. https://doi.org/10.64898/2026.01.08.698370 DOI: https://doi.org/10.64898/2026.01.08.698370

Shikha, D., Kumar, A., Jakhar, P., Serre, N., Koolath, V., Bhardwaj, S.,…Satbhai, S. B. (2026). Danger-associated peptide modulates iron deficiency signaling and root growth in Arabidopsis. New Phytologist, 249(4), 1890-1908. https://doi.org/https://doi.org/10.1111/nph.70792 DOI: https://doi.org/10.1111/nph.70792

Shin, L.-J., Lo, J.-C., Chen, G. H., Callis, J., Fu, H., & Yeh, K.-C. (2013). IRT1 DEGRADATION FACTOR1, a RING E3 Ubiquitin Ligase, Regulates the Degradation of IRON-REGULATED TRANSPORTER1 in Arabidopsis. The Plant Cell, 25, 3039-3051. https://doi.org/10.1105/tpc.113.115212 DOI: https://doi.org/10.1105/tpc.113.115212

Shinde, M. Y., Sidoli, S., Kulej, K., Mallory, M. J., Radens, C. M., Reicherter, A. L.,…Garcia, B. A. (2017). Phosphoproteomics reveals that glycogen synthase kinase-3 phosphorylates multiple splicing factors and is associated with alternative splicing. Journal of Biological Chemistry, 292(44), 18240-18255. DOI: https://doi.org/10.1074/jbc.M117.813527

Song, S., Zhang, N., Fan, X., & Wang, G. (2025). bHLH Transcription Factors in Cereal Crops: Diverse Functions in Regulating Growth, Development and Stress Responses. International Journal of Molecular Sciences, 26(20), 9915. DOI: https://doi.org/10.3390/ijms26209915

Spielmann, J., Fanara, S., Cotelle, V., & Vert, G. (2023). Multilayered regulation of iron homeostasis in Arabidopsis. Frontiers in Plant Science, 14, 1250588. DOI: https://doi.org/10.3389/fpls.2023.1250588

Stringlis, I. A., Yu, K., Feussner, K., de Jonge, R., Van Bentum, S., Van Verk, M. C.,…Pieterse, C. M. J. (2018). MYB72-dependent coumarin exudation shapes root microbiome assembly to promote plant health. Proceedings of the National Academy of Sciences, 115(22), E5213-E5222. https://doi.org/doi:10.1073/pnas.1722335115 DOI: https://doi.org/10.1073/pnas.1722335115

Tabata, R. (2023). Regulation of the iron-deficiency response by IMA/FEP peptide. Front Plant Sci, 14, 1107405. https://doi.org/10.3389/fpls.2023.1107405 DOI: https://doi.org/10.3389/fpls.2023.1107405

Tang, D., Wang, G., & Zhou, J.-M. (2017). Receptor kinases in plant-pathogen interactions: more than pattern recognition. The Plant Cell, 29(4), 618-637. DOI: https://doi.org/10.1105/tpc.16.00891

Trofimov, K., Mankotia, S., Ngigi, M., Baby, D., Satbhai, S. B., & Bauer, P. (2025). Shedding light on iron nutrition: exploring intersections of transcription factor cascades in light and iron deficiency signaling. Journal of experimental botany, 76(3), 787-802. DOI: https://doi.org/10.1093/jxb/erae324

Tsuchida, N., Lee, T.-H., Leiwakabessy, M., Yamashita, K., Hiruma, K., Okada, K.,…Cosentino, S. (2026). Iron-dependent reprogramming of damage-associated peptide receptor signaling coordinates immunity and phosphate stress adaptation. bioRxiv, 2026.2003. 2009.710003. DOI: https://doi.org/10.64898/2026.03.09.710003

Verma, M. (2025). Mapping chemical and genetic regulators of aryl hydrocarbon receptor signaling. Harvard University.

Wang, R., Fei, Y., Pan, Y., Zhou, P., Adegoke, J. O., Shen, R., & Lan, P. (2023). IMA peptides function in iron homeostasis and cadmium resistance. Plant Science, 336, 111868. DOI: https://doi.org/10.1016/j.plantsci.2023.111868

Wang, Y., Li, X., Fan, B., Zhu, C., & Chen, Z. (2021). Regulation and function of defense-related callose deposition in plants. International Journal of Molecular Sciences, 22(5), 2393. DOI: https://doi.org/10.3390/ijms22052393

Wu, H., & Ling, H.-Q. (2019). FIT-binding proteins and their functions in the regulation of Fe homeostasis. Frontiers in Plant Science, 10, 844. DOI: https://doi.org/10.3389/fpls.2019.00844

Wu, H., & Ling, H. Q. (2019). FIT-Binding Proteins and Their Functions in the Regulation of Fe Homeostasis. Front Plant Sci, 10, 844. https://doi.org/10.3389/fpls.2019.00844 DOI: https://doi.org/10.3389/fpls.2019.00844

Xie, Y., Shan, L., & He, P. (2026). Cell surface receptors integrate plant immunity, stress adaptation, and nutrient acquisition. Trends in plant science. DOI: https://doi.org/10.1016/j.tplants.2026.04.013

Yu, Q., Li, X., He, J., Feng, Y., Kang, J., Chen, L.,…Yang, Y. (2026). CARK3-mediated phosphorylation of bHLH106 inhibits iron uptake by repressing the expression of IRT1 in Arabidopsis. Plant Communications. DOI: https://doi.org/10.1016/j.xplc.2026.102030

Yuan, Y., Wu, H., Wang, N., Li, J., Zhao, W., Du, J.,…Ling, H.-Q. (2008). FIT interacts with AtbHLH38 and AtbHLH39 in regulating iron uptake gene expression for iron homeostasis in Arabidopsis. Cell research, 18(3), 385-397. DOI: https://doi.org/10.1038/cr.2008.26

Zaid, A., Ahmad, B., Jaleel, H., Wani, S. H., & Hasanuzzaman, M. (2020). A critical review on iron toxicity and tolerance in plants: role of exogenous phytoprotectants. Plant micronutrients: Deficiency and toxicity management, 83-99. DOI: https://doi.org/10.1007/978-3-030-49856-6_4

Zamioudis, C., Hanson, J., & Pieterse, C. M. J. (2014). β-Glucosidase BGLU42 is a MYB72-dependent key regulator of rhizobacteria-induced systemic resistance and modulates iron deficiency responses in Arabidopsis roots. New Phytologist, 204(2), 368-379. https://doi.org/https://doi.org/10.1111/nph.12980 DOI: https://doi.org/10.1111/nph.12980

Zhang, J., Liu, B., Li, M., Feng, D., Jin, H., Wang, P.,…Wang, H.-B. (2015). The bHLH Transcription Factor bHLH104 Interacts with IAA-LEUCINE RESISTANT3 and Modulates Iron Homeostasis in Arabidopsis. The Plant Cell, 27(3), 787-805. https://doi.org/10.1105/tpc.114.132704 DOI: https://doi.org/10.1105/tpc.114.132704

Zhang, X., Zhang, D., Sun, W., & Wang, T. (2019). The adaptive mechanism of plants to iron deficiency via iron uptake, transport, and homeostasis. International Journal of Molecular Sciences, 20(10), 2424. DOI: https://doi.org/10.3390/ijms20102424

Zhang, Z., Cheng, J., Wang, W., Gao, Y., Xian, X., Li, C., & Wang, Y. (2023). Transcription factors dealing with iron‐deficiency stress in plants: focus on the bHLH transcription factor family. Physiologia plantarum, 175(6), e14091. DOI: https://doi.org/10.1111/ppl.14091

Downloads

Published

12-10-2026

How to Cite

SRF3-bHLH Crosstalk in Arabidopsis Iron Homeostasis: Receptor Kinase Signaling, Transcriptional Regulation and Genetic Epistasis (Z. Haider, S. F. Imran, A. Raza, A. Latif, M. Saleem, & M. Amir, Trans.). (2026). Journal of Applied Research in Plant Sciences, 7(02), 183-194. https://doi.org/10.38211/joarps.2026.07.368

Similar Articles

1-10 of 118

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)