The transcription factor SbbHLH168 enhances salt tolerance by coordinating ion homeostasis and lignin content in sorghum

Simin Li , Zishuo Han , Rui Liu , Zengting Chen , Xuemei Wang , Na Sui , Zhiying Zhao

Stress Biology ›› 2026, Vol. 6 ›› Issue (1) : 51

PDF
Stress Biology ›› 2026, Vol. 6 ›› Issue (1) :51 DOI: 10.1007/s44154-026-00330-4
Original Paper
research-article
The transcription factor SbbHLH168 enhances salt tolerance by coordinating ion homeostasis and lignin content in sorghum
Author information +
History +
PDF

Abstract

Soil salinization is an escalating global threat to crop productivity. Here, we demonstrate that the sorghum bHLH transcription factor SbbHLH168 is a central regulator of salt-stress tolerance. SbbHLH168 is nuclear-localized, constitutively expressed in all organs and rapidly up-regulated by NaCl. Overexpression of SbbHLH168 in either Arabidopsis or sorghum conferred markedly higher biomass retention, longer roots, lower relative electrical conductivity, less accumulation of superoxide and H₂O₂, and lower Na⁺/K⁺ ratio through decreased Na⁺ accumulation under salt stress, whereas VIGS silent groups displayed the opposite phenotype. qRT-PCR and biochemical assays demonstrated that SbbHLH168 up-regulates key lignin-biosynthetic genes (SbC4H, SbF5H, SbCOMT1) and increases root lignin content under salt stress, thereby reinforcing cell-wall integrity and limiting ion leakage. Furthermore, yeast two-hybrid and BiFC assays confirmed that SbbHLH168 interacts with SbbHLH35 in the nucleus, indicating that SbbHLH168's functional activity depends on heterodimerization with SbbHLH35. Collectively, SbbHLH168 integrates ion homeostasis, ROS scavenging and lignin content to confer salt tolerance, providing a direct gene target for molecular breeding of resilient sorghum cultivars.

Keywords

Salt stress / SbbHLH168 / SbbHLH35 / Lignin content / Sorghum

Cite this article

Download citation ▾
Simin Li, Zishuo Han, Rui Liu, Zengting Chen, Xuemei Wang, Na Sui, Zhiying Zhao. The transcription factor SbbHLH168 enhances salt tolerance by coordinating ion homeostasis and lignin content in sorghum. Stress Biology, 2026, 6 (1) : 51 DOI:10.1007/s44154-026-00330-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Alam MS, Yang ZK, Li C, Yan Y, Liu Z, Nazir MM, Xu JH. Loss-of-function mutations of OsbHLH044 transcription factor lead to salinity sensitivity and a greater chalkiness in rice (Oryza sativa L.). Plant Physiol Biochem, 2022, 193: 110-123

[2]

Asano T, Hayashi N, Kobayashi M, Aoki N, Miyao A, Mitsuhara I, Ichikawa H, Komatsu S, Hirochika H, Kikuchi S, Ohsugi R. A rice calcium-dependent protein kinase OsCPK12 oppositely modulates salt-stress tolerance and blast disease resistance. Plant J, 2012, 69(1): 26-36

[3]

Bassil E, Blumwald E. The ins and outs of intracellular ion homeostasis: NHX-type cation/H(+) transporters. Curr Opin Plant Biol, 2014, 22: 1-6

[4]

Chen Y, Li F, Ma Y, Chong K, Xu Y. Overexpression of OrbHLH001, a putative helix-loop-helix transcription factor, causes increased expression of AKT1 and maintains ionic balance under salt stress in rice. J Plant Physiol, 2013, 170(1): 93-100

[5]

Chen C, Ge F, Du H, Sun Y, Sui Y, Tang S, Shen Z, Li X, Zhang H, Mei C, Xie P, Li C, Yang S, Wei H, Shi J, Zhang D, Zhao K, Yang D, Qiao Y, Luo Z, Zhang L, Khan A, Wodajo B, Wu Y, Xia R, Wu C, Liang C, Xie Q, Yu F. A comprehensive omics resource and genetic tools for functional genomics research and genetic improvement of sorghum. Mol Plant, 2025, 18(4): 703-719

[6]

Cui B, Liu R, Flowers TJ, Song J. Casparian bands and suberin lamellae: key targets for breeding salt tolerant crops?. Environ Exp Bot, 2021, 191 104600

[7]

Dahlberg J. The role of sorghum in renewables and biofuels. Methods Mol Biol, 2019, 1931: 269-277

[8]

Dong Y, Wang C, Han X, Tang S, Liu S, Xia X, Yin W. A novel bHLH transcription factor PebHLH35 from Populus euphratica confers drought tolerance through regulating stomatal development, photosynthesis and growth in Arabidopsis. Biochem Biophys Res Commun, 2014, 450(1): 453-458

[9]

Duchenne-Moutien RA, Neetoo H. Climate change and emerging food safety issues: a review. J Food Prot, 2021, 84(11): 1884-1897

[10]

Feller A, Machemer K, Braun EL, Grotewold E. Evolutionary and comparative analysis of MYB and bHLH plant transcription factors. Plant J, 2011, 66(1): 94-116

[11]

Hao H, Li Z, Leng C, Lu C, Luo H, Liu Y, Wu X, Liu Z, Shang L, Jing HC. Sorghum breeding in the genomic era: opportunities and challenges. Theor Appl Genet, 2021, 134(7): 1899-1924

[12]

Hao R, Zhou W, Li J, Luo M, Scheres B, Guo Y. On salt stress, PLETHORA signaling maintains root meristems. Dev Cell, 2023, 58(18): 1657-1669.e5

[13]

Hernandez JM, Feller A, Morohashi K, Frame K, Grotewold E. The basic helix loop helix domain of maize R links transcriptional regulation and histone modifications by recruitment of an EMSY-related factor. Proc Natl Acad Sci U S A, 2007, 104(43): 17222-17227

[14]

Jiang Y, Yang B, Deyholos MK. Functional characterization of the Arabidopsis bHLH92 transcription factor in abiotic stress. Mol Genet Genomics, 2009, 282(5): 503-516

[15]

Jiang L, Tian X, Li S, Fu Y, Xu J, Wang G. The AabHLH35 transcription factor identified from Anthurium andraeanum is involved in cold and drought tolerance. Plants (Basel), 2019, 8(7 216

[16]

Johnson R, Puthur JT. Seed priming as a cost effective technique for developing plants with cross tolerance to salinity stress. Plant Physiol Biochem, 2021, 162: 247-257

[17]

Lakra N, Nutan KK, Das P, Anwar K, Singla-Pareek SL, Pareek A. A nuclear-localized histone-gene binding protein from rice (OsHBP1b) functions in salinity and drought stress tolerance by maintaining chlorophyll content and improving the antioxidant machinery. J Plant Physiol, 2015, 176: 36-46

[18]

Lee S, Jeon D, Choi S, Kang Y, Seo S, Kwon S, Lyu J, Ahn J, Seo J, Kim C. Expression profile of sorghum genes and cis-regulatory elements under salt-stress conditions. Plants (Basel), 2022, 117 869

[19]

Lei R, Li Y, Cai Y, Li C, Pu M, Lu C, Yang Y, Liang G. bHLH121 functions as a direct link that facilitates the activation of FIT by bHLH IVc transcription factors for maintaining Fe homeostasis in Arabidopsis. Mol Plant, 2020, 134): 634-649

[20]

Liang X, Li J, Yang Y, Jiang C, Guo Y. Designing salt stress-resilient crops: current progress and future challenges. J Integr Plant Biol, 2024, 66(3): 303-329

[21]

Liu C, Mao B, Ou S, Wang W, Liu L, Wu Y, Chu C, Wang X. OsbZIP71, a bZIP transcription factor, confers salinity and drought tolerance in rice. Plant Mol Biol, 2014, 84(1–2): 19-36

[22]

Moreno JE, Moreno-Piovano G, Chan RL. The antagonistic basic helix-loop-helix partners BEE and IBH1 contribute to control plant tolerance to abiotic stress. Plant Sci, 2018, 271: 143-150

[23]

Onohata T, Gomi K. Overexpression of jasmonate-responsive OsbHLH034 in rice results in the induction of bacterial blight resistance via an increase in lignin biosynthesis. Plant Cell Rep, 2020, 39(9): 1175-1184

[24]

Pan W, Zheng P, Zhang C, Wang W, Li Y, Fan T, Liu Y, Cao S. The effect of ABRE BINDING FACTOR 4-mediated FYVE1 on salt stress tolerance in Arabidopsis. Plant Sci, 2020, 296 110489

[25]

Park HJ, Kim WY, Yun DJ. A new insight of salt stress signalingin plant. Mol Cells, 2016, 39(6): 447-459

[26]

Qiao Q, Huang Y, Dong H, Xing C, Han C, Lin L, Wang X, Su Z, Qi K, Xie Z, Huang X, Zhang S. The PbbHLH62/PbVHA-B1 module confers salt tolerance through modulating intracellular Na+/K+ homeostasis and reactive oxygen species removal in pear. Plant Physiol Biochem, 2024, 210 108663

[27]

Rabeh K, Hnini M, Oubohssaine M. A comprehensive review of transcription factor-mediated regulation of secondary metabolites in plants under environmental stress. Stress Biol, 2025, 5: 15

[28]

Schwacke R, Schneider A, van der Graaff E, Fischer K, Catoni E, Desimone M, Frommer WB, Flügge UI, Kunze R. ARAMEMNON, a novel database for Arabidopsis integral membrane proteins. Plant Physiol, 2003, 131(1): 16-26

[29]

Shu L, Li L, Jiang YQ, Yan J. Advances in membrane-tethered NAC transcription factors in plants. Plant Sci, 2024, 342 112034

[30]

Song Y, Zheng H, Sui Y, Li S, Wu F, Sun X, Sui N. SbWRKY55 regulates sorghum response to saline environment by its dual role in abscisic acid signaling. Theor Appl Genet, 2022, 135(8): 2609-2625

[31]

Song Y, Li S, Sui Y, Zheng H, Han G, Sun X, Yang W, Wang H, Zhuang K, Kong F, Meng Q, Sui N. SbbHLH85, a bHLH member, modulates resilience to salt stress by regulating root hair growth in sorghum. Theor Appl Genet, 2022, 135(1): 201-216

[32]

Sui N, Tian S, Wang W, Wang M, Fan H. Overexpression of glycerol-3-phosphate acyltransferase from Suaeda salsa improves salt tolerance in arabidopsis. Front Plant Sci, 2017, 8: 1337

[33]

Toda Y, Tanaka M, Ogawa D, Kurata K, Kurotani K, Habu Y, Ando T, Sugimoto K, Mitsuda N, Katoh E, Abe K, Miyao A, Hirochika H, Hattori T, Takeda S. RICE SALT SENSITIVE3 forms a ternary complex with JAZ and class-C bHLH factors and regulates jasmonate-induced gene expression and root cell elongation. Plant Cell, 2013, 25(5): 1709-1725

[34]

Wan W, Zhang L, Liu X, Cui H, Shi M, Sun H, Yang W, Wang X, Yang F, Jin S. BLH3 regulates the ABA pathway and lignin synthesis under salt stress in Lilium pumilum. Plants (Basel), 2025, 14(12 1860

[35]

Waseem M, Rong X, Li Z. Dissecting the role of a basic helix-loop-helix transcription factor, SlbHLH22, under salt and drought stresses in transgenic solanum lycopersicum L. Front Plant Sci, 2019, 410): 734

[36]

Wu Z, Wang N, Hisano H, Cao Y, Wu F, Liu W, Bao Y, Wang ZY, Fu C. Simultaneous regulation of F5H in COMT-RNAi transgenic switchgrass alters effects of COMT suppression on syringyl lignin biosynthesis. Plant Biotechnol J, 2019, 17(4): 836-845

[37]

Xie Q, Xu Z. Sustainable agriculture: from sweet sorghum planting and ensiling to ruminant feeding. Mol Plant, 2019, 12(5): 603-606

[38]

Yamaguchi T, Hamamoto S, Uozumi N. Sodium transport system in plant cells. Front Plant Sci, 2013, 4 410

[39]

Yang Z, Zheng HX, Wei XC, Song J, Wang BS, Sui N (2018) Transcriptome analysis of sweet sorghum inbred lines differing in salt tolerance provides novel insights into salt exclusion by roots. Plant Soil 430:423–439. https://doi.org/10.1007/s11104-018-3736-0

[40]

Zhai Y, Zhang L, Xia C, Fu S, Zhao G, Jia J, Kong X. The wheat transcription factor, TabHLH39, improves tolerance to multiple abiotic stressors in transgenic plants. Biochem Biophys Res Commun, 2016, 473(4): 1321-1327

[41]

Zhang J, Yu D, Zhang Y, Liu K, Xu K, Zhang F, Wang J, Tan G, Nie X, Ji Q, Zhao L, Li C. Vacuum and co-cultivation agroinfiltration of (Germinated) seeds results in Tobacco Rattle Virus (TRV) mediated whole-plant Virus-Induced Gene Silencing (VIGS) in wheat and maize. Front Plant Sci, 2017, 8: 393

[42]

Zhang H, Yu F, Xie P, Sun S, Qiao X, Tang S, Chen C, Yang S, Mei C, Yang D, Wu Y, Xia R, Li X, Lu J, Liu Y, Xie X, Ma D, Xu X, Liang Z, Feng Z, Huang X, Yu H, Liu G, Wang Y, Li J, Zhang Q, Chen C, Ouyang Y, Xie Q. A Gγ protein regulates alkaline sensitivity in crops. Science, 2023, 379(6638 eade8416

[43]

Zhang H, Guo J, Chen X, Zhou Y, Pei Y, Chen L, Ul Haq S, Lu M, Gong H, Chen R (2022) Pepper bHLH transcription factor CabHLH035 contributes to salt tolerance by modulating ion homeostasis and proline biosynthesis. Hortic Res 9:uhac203. https://doi.org/10.1093/hr/uhac203

[44]

Zheng H, Gao Y, Sui Y, Dang Y, Wu F, Wang X, Zhang F, Du X, Sui N. R2R3 MYB transcription factor SbMYBHv33 negatively regulates sorghum biomass accumulation and salt tolerance. Theor Appl Genet, 2023, 1361): 5

[45]

Zhou H, Shi H, Yang Y, Feng X, Chen X, Xiao F, Lin H, Guo Y. Insights into plant salt stress signaling and tolerance. J Genet Genomics, 2024, 51(1): 16-34

[46]

Zuo ZF, Lee HY, Kang HG (2023). Basic Helix-Loop-Helix Transcription Factors: Regulators for Plant Growth Development and Abiotic Stress Responses. Int J Mol Sci 24(2):1419. https://doi.org/10.3390/ijms24021419

Funding

National Natural Science Research Foundation of China(32301746)

Natural Science Foundation of Shandong Province(No. ZR2023QC192)

National Key R&D Program of China(2023YFD200140201)

Modern Agriculture Industrial Technology Systems Project of Shandong Province(SDAIT-15-04)

the special fund for TaiShan Scholars(No. tsqn202211106)

the special fund for TaiShan Scholars(No. tsqn20250718)

RIGHTS & PERMISSIONS

The Author(s)

PDF

0

Accesses

0

Citation

Detail

Sections
Recommended

/