Editing the message: 3′UTR cis-regulatory elements at the nexus of post-transcriptional regulation and crop improvement
Zeqin Zhang , Sirui Liu , Saikat Paul , Michitaka Notaguchi , Wenna Zhang , Munenori Kitagawa
Horticulture Advances ›› 2026, Vol. 4 ›› Issue (1) : 23
Climate change and soil degradation pose increasingly serious threats to global food security, highlighting the need for continued innovation and diversification in plant breeding strategies. Plant growth and development rely on precise and dynamic regulation of gene expression that enables rapid responses to environmental cues. Increasing evidence highlights the central roles of cis-regulatory elements (CREs), including RNA sequence motifs, RNA modifications, and secondary or tertiary RNA structures, in post-transcriptional control. These CREs are enriched within the untranslated regions (UTRs) of plant mRNAs. In this review, we summarize the diverse CREs characterized to date, particularly those located within the 3′UTR, and describe how they function together with trans-acting factors like RNA-binding proteins to regulate mRNA stability, translation efficiency, subcellular localization, and non-cell-autonomous mobility. These processes constitute key mechanisms for the spatiotemporal regulation of gene expression that underlies plant environmental responses and resilience. We further discuss emerging opportunities and challenges in harnessing 3′UTR CREs as targets and tools for next-generation crop improvement. By integrating recent advances in post-transcriptional biology with molecular breeding frameworks, 3′UTR CREs offer a promising framework for achieving precise, tunable, and robust regulation of agronomically important traits.
3′ untranslated region (3′UTR) / Cis-regulatory elements / Post-transcriptional regulation / N6-methyladenosine (m6A) / RNA structure / Crop breeding
| [1] |
|
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
Cai Y, Cheng L, Liu X, Li R, Liu Y, Ge S, et al. SlALKBH9B is involved in drought-induced flower drop by regulating ethylene production. Hortic Res. 2025;12:uhaf173. https://doi.org/10.1093/hr/uhaf173. |
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
Chen Y, Yin S, Yang Y, Xie K. The dsRNA-binding protein OsDRB1.4 is phosphorylated by OsMPK5 and negatively regulates rice defense against Magnaporthe oryzae. Plant J. 2025;122:e70285. https://doi.org/10.1111/tpj.70285. |
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
|
| [19] |
Due Tankmar M, Reichel M, Arribas-Hernández L, Brodersen P. A YTHDF–PABP interaction is required for m6A-mediated organogenesis in plants. EMBO Rep. 2023;24:e57741. https://doi.org/10.15252/embr.202357741. |
| [20] |
|
| [21] |
|
| [22] |
Gao Y, Bian H, Wang H, Wang J, Ye B, Zhang C, et al. The m6A reader SlYTH1 regulates flavor-related volatiles biosynthesis via affecting mRNA stability and translation in tomato fruit. Plant Physiol. 2025;198:kiaf245. https://doi.org/10.1093/plphys/kiaf245. |
| [23] |
|
| [24] |
|
| [25] |
|
| [26] |
|
| [27] |
|
| [28] |
|
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
|
| [39] |
|
| [40] |
|
| [41] |
|
| [42] |
|
| [43] |
|
| [44] |
|
| [45] |
|
| [46] |
|
| [47] |
|
| [48] |
|
| [49] |
|
| [50] |
|
| [51] |
Lewinski M, Steffen A, Kachariya N, Elgner M, Schmal C, Messini N, et al. Arabidopsis thaliana GLYCINE RICH RNA-BINDING PROTEIN 7 interaction with its iCLIP target LHCB1.1 correlates with changes in RNA stability and circadian oscillation. Plant J. 2024;118:203–24. https://doi.org/10.1111/tpj.16601. |
| [52] |
|
| [53] |
|
| [54] |
Li Y, Zhu S. Polar localization and local translation of RHO-RELATED PROTEIN FROM PLANTS2 mRNAs promote root hair growth in Arabidopsis. Plant Cell. 2024;37:koae333. https://doi.org/10.1093/plcell/koae333. |
| [55] |
|
| [56] |
|
| [57] |
|
| [58] |
|
| [59] |
|
| [60] |
|
| [61] |
|
| [62] |
|
| [63] |
|
| [64] |
|
| [65] |
|
| [66] |
|
| [67] |
|
| [68] |
|
| [69] |
|
| [70] |
|
| [71] |
|
| [72] |
|
| [73] |
|
| [74] |
|
| [75] |
Shi Y, Yang S, Pei T, Xu Y, Zhao Y, Xue H, et al. The m6A writers, readers, and erasers regulate plant development and respond to biotic/abiotic stresses. Epigenetics Insights. 2025;18:e008. https://doi.org/10.48130/epi-0025-0007. |
| [76] |
|
| [77] |
|
| [78] |
|
| [79] |
|
| [80] |
|
| [81] |
|
| [82] |
|
| [83] |
|
| [84] |
|
| [85] |
|
| [86] |
|
| [87] |
|
| [88] |
|
| [89] |
|
| [90] |
Wang J, Li Y, Hu Y, Zhu S. Jasmonate induces translation of the Arabidopsis transfer RNA-binding protein YUELAO1, which activates MYC2 in jasmonate signaling. Plant Cell. 2024c;37:koae294. https://doi.org/10.1093/plcell/koae294. |
| [91] |
|
| [92] |
|
| [93] |
|
| [94] |
|
| [95] |
|
| [96] |
|
| [97] |
|
| [98] |
|
| [99] |
|
| [100] |
|
| [101] |
|
| [102] |
|
| [103] |
|
| [104] |
|
| [105] |
|
| [106] |
|
| [107] |
|
| [108] |
|
| [109] |
|
| [110] |
|
| [111] |
|
| [112] |
|
| [113] |
|
| [114] |
|
| [115] |
|
| [116] |
|
The Author(s)
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