Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Nature Communications
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. nature communications
  3. articles
  4. article
Phytochrome B integrates jasmonic acid and warm temperature signaling pathways to regulate cotyledon chloroplast development
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 09 March 2026

Phytochrome B integrates jasmonic acid and warm temperature signaling pathways to regulate cotyledon chloroplast development

  • Peipei Qi1,2 na1,
  • Junling Huai1,3 na1,
  • Nan Gao1,
  • Yuanyuan Yao1,3 &
  • …
  • Rongcheng Lin  ORCID: orcid.org/0000-0001-8346-33901,2 

Nature Communications , Article number:  (2026) Cite this article

  • 2212 Accesses

  • 6 Altmetric

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Chloroplasts
  • Jasmonic acid
  • Plant signalling

Abstract

Chloroplast biogenesis and development are coordinated by both endogenous factors and environmental cues. The interplay between jasmonic acid (JA) and temperature in regulating chloroplast development remains poorly understood. Here, we demonstrate that methyl jasmonate (MeJA) and warm temperature (28 °C) treatments additively impair chlorophyll accumulation and chloroplast development in Arabidopsis thaliana cotyledons. We found that the thermosensor phytochrome B (phyB) suppresses, whereas the JA receptor CORONATINE INSENSITIVE 1 (COI1) promotes, MeJA- and warm temperature-mediated chloroplast development. Moreover, phyB directly interacts with JASMONATE ZIM-DOMAIN 1 (JAZ1) and JAZ3, preventing their JA-induced degradation, and warm temperature attenuates this interaction. Strikingly, we reveal that transcription factors ELONGATED HYPOCOTYL 5 (HY5) and MYC2 oppositely regulate cotyledon chloroplast development in response to MeJA and warm temperature by directly and differentially modulating downstream transcriptional networks. Our study establishes a molecular framework in which phyB integrates JA and warm temperature signaling through the HY5-MYCs transcriptional regulatory network to fine-tune chloroplast development, highlighting a plant strategy for ecological adaptation.

Similar content being viewed by others

Warm temperature triggers JOX and ST2A-mediated jasmonate catabolism to promote plant growth

Article Open access 10 August 2021

Extended JAZ degron sequence for plant hormone binding in jasmonate co-receptor of tomato SlCOI1-SlJAZ

Article Open access 30 June 2021

Methyl jasmonate-loaded chitosan nanoparticles and biochar improve maize thermotolerance

Article Open access 05 February 2026

Data availability

All data generated or analyzed in this study are available in the main text and the Supplementary Information. Sequence data from this article can be found in the GenBank/EMBL data libraries under the following accession numbers: COI1 (AT2G39940), phyB (AT2G18790), JAZ1 (AT1G19180), JAZ3 (AT3G17860), HY5 (AT5G11260), MYC2 (AT1G32640), MYC3 (AT5G46760), MYC4 (AT4G17880), MES16 (AT4G16690), RAP2.6 (AT1G43160), RAP2.6 L (AT5G13330), SAG21 (AT4G02380), SAG20 (AT3G10985), SOC1 (AT2G45660), NYC1 (AT4G13250), SRG1 (AT1G17020), WAG2 (AT3G14370), CRF2 (AT4G23750), NCED3 (AT3G14440), COR15B (AT2G42530), MYB47 (AT1G18710), ACBP3 (AT4G24230), HSP101 (AT1G74310), LTI65 (AT5G52300), LTI78 (AT5G52310), GLK1 (AT2G20570), GLK2 (AT5G44190), ACTIN7 (AT5G09810), and UBQ1 (AT3G52590). All the unprocessed data, gels, and blots were provided in the Source Data file. Source data are provided with this paper.

References

  1. Lobell, D. B., Schlenker, W. & Costa-Roberts, J. Climate trends and global crop production since 1980. Science 333, 616–620 (2011).

    Google Scholar 

  2. Zhao, C. et al. Temperature increase reduces global yields of major crops in four independent estimates. Proc. Natl. Acad. Sci. USA 114, 9326–9331 (2017).

    Google Scholar 

  3. Casal, J. J. & Balasubramanian, S. Thermomorphogenesis. Annu. Rev. Plant Biol. 70, 321–346 (2019).

    Google Scholar 

  4. Quint, M. et al. Molecular and genetic control of plant thermomorphogenesis. Nat. Plants 2, 15190 (2016).

    Google Scholar 

  5. Li, J., Li, G., Wang, H. & Wang Deng, X. Phytochrome signaling mechanisms. Arabidopsis Book 9, e0148 (2011).

    Google Scholar 

  6. Leivar, P. & Quail, P. H. PIFs: pivotal components in a cellular signaling hub. Trends Plant Sci. 16, 19–28 (2011).

    Google Scholar 

  7. Klose, C., Nagy, F. & Schäfer, E. Thermal reversion of plant phytochromes. Mol. Plant 13, 386–397 (2020).

    Google Scholar 

  8. Chen, D. et al. Integration of light and temperature sensing by liquid-liquid phase separation of phytochrome B. Mol. Cell 82, 3015–3029 (2022).

    Google Scholar 

  9. Jung et al. Phytochromes function as thermosensors in Arabidopsis. Science 354, 886–889 (2016).

    Google Scholar 

  10. Legris et al. Phytochrome B integrates light and temperature signals in Arabidopsis. Science 354, 897–900 (2016).

    Google Scholar 

  11. Koini, M. A. et al. High temperature-mediated adaptations in plant architecture require the bHLH transcription factor PIF4. Curr. Biol. 19, 408–413 (2009).

    Google Scholar 

  12. Kim, C. et al. High ambient temperature accelerates leaf senescence via phytochrome-interacting factor 4 and 5 in Arabidopsis. Mol. Cells 43, 645–661 (2020).

    Google Scholar 

  13. Foreman, J. et al. Light receptor action is critical for maintaining plant biomass at warm ambient temperatures. Plant J. 65, 441–452 (2011).

    Google Scholar 

  14. Hong, J. et al. Reframing agriculture by light: the role of light-mediated jasmonates/salicylic acid regulation in plant defense, development and beyond. Veg. Res. 4, e027 (2024).

    Google Scholar 

  15. Li, C. et al. Jasmonate signaling pathway modulates plant defense, growth, and their trade-offs. Int. J. Mol. Sci. 23, 3945 (2022).

    Google Scholar 

  16. Chini, A. et al. The JAZ family of repressors is the missing link in jasmonate signalling. Nature 448, 666–671 (2007).

    Google Scholar 

  17. Fernandez-Calvo, P. et al. The Arabidopsis bHLH transcription factors MYC3 and MYC4 are targets of JAZ repressors and act additively with MYC2 in the activation of jasmonate responses. Plant Cell 23, 701–715 (2011).

    Google Scholar 

  18. Wang, Y., Mostafa, S., Zeng, W., & Jin, B. Function and Mechanism of Jasmonic Acid in Plant Responses to Abiotic and Biotic Stresses. Int. J. Mol. Sci. 22, 8568 (2021).

  19. Xu, L. et al. The SCF(COI1) ubiquitin-ligase complexes are required for jasmonate response in Arabidopsis. Plant Cell 14, 1919–1935 (2002).

    Google Scholar 

  20. Hu, S., Yu, K., Yan, J., Shan, X. & Xie, D. Jasmonate perception: Ligand–receptor interaction, regulation, and evolution. Mol. Plant 16, 23–42 (2023).

    Google Scholar 

  21. Zhu, X. et al. Jasmonic acid promotes degreening via MYC2/3/4- and ANAC019/055/072-mediated regulation of major chlorophyll catabolic genes. Plant J. 84, 597–610 (2015).

    Google Scholar 

  22. Qi, T. et al. Regulation of Jasmonate-Induced Leaf Senescence by Antagonism between bHLH Subgroup IIIe and IIId Factors in Arabidopsis. Plant Cell 27, 1634–1649 (2015).

    Google Scholar 

  23. Zhu, T. et al. Warm temperature triggers JOX and ST2A-mediated jasmonate catabolism to promote plant growth. Nat. Commun. 12, 4804 (2021).

    Google Scholar 

  24. Fernandez-Milmanda, G. L. et al. A light-dependent molecular link between competition cues and defence responses in plants. Nat. Plants 6, 223–230 (2020).

    Google Scholar 

  25. Huai, J. et al. JASMONATE ZIM-domain protein 3 regulates photomorphogenesis and thermomorphogenesis through inhibiting PIF4 in Arabidopsis. Plant Physiol. 195, 2274–2288 (2024).

    Google Scholar 

  26. Thines, B. et al. JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling. Nature 448, 661–665 (2007).

    Google Scholar 

  27. Toledo-Ortiz, G. et al. The HY5-PIF regulatory module coordinates light and temperature control of photosynthetic gene transcription. PLoS Genet 10, e1004416 (2014).

    Google Scholar 

  28. Liu, X., Li, Y. & Zhong, S. Interplay between light and plant hormones in the control of Arabidopsis seedling chlorophyll biosynthesis. Front. Plant Sci. 8, 1433 (2017).

    Google Scholar 

  29. Xiao, Y. et al. HY5: a pivotal regulator of light-dependent development in higher plants. Front. Plant Sci. 12, 800989 (2022).

    Google Scholar 

  30. Song, C. et al. The multifaceted roles of MYC2 in plants: Toward transcriptional reprogramming and stress tolerance by jasmonate signaling. Front. Plant Sci. 13, 868874 (2022).

    Google Scholar 

  31. Ortigosa, A. et al. The JA-pathway MYC transcription factors regulate photomorphogenic responses by targeting HY5 gene expression. Plant J. 102, 138–152 (2020).

    Google Scholar 

  32. Cheng, Y., Qin, G., Dai, X., & Zhao, Y. NPY genes and AGC kinases define two key steps in auxin-mediated organogenesis in Arabidopsis. Proc. Natl. Acad. Sci. USA 105, 21017–21022 (2008).

  33. Rashotte, A. M. et al. A subset of Arabidopsis AP2 transcription factors mediates cytokinin responses in concert with a two-component pathway. Proc. Natl. Acad. Sci. USA 103, 11081–11085 (2006).

    Google Scholar 

  34. Kim, H. J., Nam, H. G. & Lim, P. O. Regulatory network of NAC transcription factors in leaf senescence. Curr. Opin. Plant Biol. 33, 48–56 (2016).

    Google Scholar 

  35. Li, Y. et al. Regulatory and retrograde signaling networks in the chlorophyll biosynthetic pathway. J. Integr. Plant Biol. 67, 887–911 (2025).

    Google Scholar 

  36. de Ollas, C. & Dodd, I. C. Physiological impacts of ABA–JA interactions under water-limitation. Plant Mol. Biol. 91, 641–650 (2016).

    Google Scholar 

  37. Moreno, J. E., Tao, Y., Chory, J. & Ballare, C. L. Ecological modulation of plant defense via phytochrome control of jasmonate sensitivity. Proc. Natl. Acad. Sci. USA 106, 4935–4940 (2009).

    Google Scholar 

  38. Agrawal, A. A., Kearney, E. E., Hastings, A. P. & Ramsey, T. E. Attenuation of the jasmonate burst, plant defensive traits, and resistance to specialist monarch caterpillars on shaded common milkweed (Asclepias syriaca). J. Chem. Ecol. 38, 893–901 (2012).

    Google Scholar 

  39. Suzuki, A. et al. Lotus japonicus nodulation is photomorphogenetically controlled by sensing the red/far red (R/FR) ratio through jasmonic acid (JA) signaling. Proc. Natl. Acad. Sci. USA 108, 16837–16842 (2011).

    Google Scholar 

  40. Zhou, Y. et al. NPR1 promotes blue light-induced plant photomorphogenesis by ubiquitinating and degrading PIF4. Proc. Natl. Acad. Sci. USA 121, e2412755121 (2024).

    Google Scholar 

  41. Xu, X., Hu, J. & Yuan, Z. Stabilization or degradation? Post-translational modifications of JAZ proteins in plants. Mol. Plant 17, 1002–1004 (2024).

    Google Scholar 

  42. Xu, L. et al. The SCFCOI1 ubiquitin-ligase complexes are required for jasmonate response in Arabidopsis. Plant Cell 14, 1919–1935 (2002).

    Google Scholar 

  43. Yan, J. et al. The Arabidopsis F-box protein CORONATINE INSENSITIVE1 is stabilized by SCFCOI1 and degraded via the 26S proteasome pathway. Plant Cell 25, 486–498 (2013).

    Google Scholar 

  44. Varshney, V. et al. The Arabidopsis F-box protein SKP1-INTERACTING PARTNER 31 modulates seed maturation and seed vigor by targeting JASMONATE ZIM DOMAIN proteins independently of jasmonic acid-isoleucine. Plant Cell 35, 3712–3738 (2023).

    Google Scholar 

  45. Wu, S. et al. The MYC2-PUB22-JAZ4 module plays a crucial role in jasmonate signaling in tomato. Mol. Plant 17, 598–613 (2024).

    Google Scholar 

  46. Sakuraba, Y. et al. Phytochrome-interacting transcription factors PIF4 and PIF5 induce leaf senescence in Arabidopsis. Nat. Commun. 5, 4636 (2014).

    Google Scholar 

  47. Zhang, Y., Liu, Z., Chen, Y., He, J. X. & Bi, Y. PHYTOCHROME-INTERACTING FACTOR 5 (PIF5) positively regulates dark-induced senescence and chlorophyll degradation in Arabidopsis. Plant Sci. 237, 57–68 (2015).

    Google Scholar 

  48. Li, J. Y., Yang, C., Tian, Y. Y. & Liu, J. X. Regulation of chloroplast development and function at adverse temperatures in plants. Plant Cell Physiol. 63, 580–591 (2022).

    Google Scholar 

  49. Zhang, T. et al. GLK transcription factors accompany ELONGATED HYPOCOTYL5 to orchestrate light-induced seedling development in Arabidopsis. Plant Physiol. 194, 2400–2421 (2024).

    Google Scholar 

  50. Yang, C. et al. HY5-HDA9 module transcriptionally regulates plant autophagy in response to light-to-dark conversion and nitrogen starvation. Mol. Plant 13, 515–531 (2020).

    Google Scholar 

  51. Yan, Y. et al. A downstream mediator in the growth repression limb of the jasmonate pathway. Plant Cell 19, 2470–2483 (2007).

    Google Scholar 

  52. Zhang, Y. & Turner, J. G. Wound-induced endogenous jasmonates stunt plant growth by inhibiting mitosis. PLoS One 3, e3699 (2008).

    Google Scholar 

  53. Noir, S. et al. Jasmonate controls leaf growth by repressing cell proliferation and the onset of endoreduplication while maintaining a potential stand-by mode. Plant Physiol. 161, 1930–1951 (2013).

    Google Scholar 

  54. Attaran, E. et al. Temporal dynamics of growth and photosynthesis suppression in response to jasmonate signaling. Plant Physiol. 165, 1302–1314 (2014).

    Google Scholar 

  55. He, Y., Fukushige, H., Hildebrand, D. F. & Gan, S. Evidence supporting a role of jasmonic acid in Arabidopsis leaf senescence. Plant Physiol. 128, 876–884 (2002).

    Google Scholar 

  56. Frangedakis, E. et al. MYB-related transcription factors control chloroplast biogenesis. Cell 187, 4859–4876 (2024).

    Google Scholar 

  57. Reed, J. W., Nagpal, P., Poole, D. S., Furuya, M. & Chory, J. Mutations in the gene for the red/far-red light receptor phytochrome B alter cell elongation and physiological responses throughout Arabidopsis development. Plant Cell 5, 147–157 (1993).

    Google Scholar 

  58. Oyama, T., Shimura, Y. & Okada, K. The Arabidopsis HY5 gene encodes a bZIP protein that regulates stimulus-induced development of root and hypocotyl. Genes Dev. 11, 2983–2995 (1997).

    Google Scholar 

  59. Li, Y. et al. Arabidopsis EXECUTER1 interacts with WRKY transcription factors to mediate plastid-to-nucleus singlet oxygen signaling. Plant Cell 35, 827–851 (2023).

    Google Scholar 

  60. Huai, J. et al. SEUSS and PIF4 coordinately regulate light and temperature signaling pathways to control plant growth. Mol. Plant 11, 928–942 (2018).

    Google Scholar 

  61. Zhang, D., Jing, Y., Jiang, Z. & Lin, R. The chromatin-remodeling factor PICKLE integrates brassinosteroid and gibberellin signaling during skotomorphogenic growth in Arabidopsis. Plant Cell 26, 2472–2485 (2014).

    Google Scholar 

  62. Fernández-Calvo, P. et al. The Arabidopsis bHLH transcription factors MYC3 and MYC4 are targets of JAZ repressors and act additively with MYC2 in the activation of jasmonate responses. Plant Cell 23, 701–715 (2011).

    Google Scholar 

  63. An, C. et al. Mediator subunit MED25 links the jasmonate receptor to transcriptionally active chromatin. Proc. Natl. Acad. Sci. USA 114, E8930–E8939 (2017).

    Google Scholar 

  64. Liu, S. et al. FHY3 interacts with phytochrome B and regulates seed dormancy and germination. Plant Physiol. 187, 289–302 (2021).

    Google Scholar 

  65. Jing, Y., Guo, Q. & Lin, R. The SNL-HDA19 histone deacetylase complex antagonizes HY5 activity to repress photomorphogenesis in Arabidopsis. N. Phytol. 229, 3221–3236 (2020).

    Google Scholar 

  66. Zhang, D., Li, Y., Zhang, X., Zha, P. & Lin, R. The SWI2/SNF2 chromatin-remodeling ATPase BRAHMA regulates chlorophyll biosynthesis in Arabidopsis. Mol. Plant 10, 155–167 (2017).

    Google Scholar 

  67. Liu, L. et al. Metabolomics and transcriptomics analysis revealed the response mechanism of alfalfa to combined cold and saline-alkali stress. Plant J. 119, 1900–1919 (2024).

    Google Scholar 

  68. Lin, R. et al. Transposase-derived transcription factors regulate light signaling in Arabidopsis. Science 318, 1302–1305 (2007).

    Google Scholar 

  69. Li, Y., Du, Y., Huai, J., Jing, Y. & Lin, R. The RNA helicase UAP56 and the E3 ubiquitin ligase COP1 coordinately regulate alternative splicing to repress photomorphogenesis in Arabidopsis. Plant Cell 34, 4191–4212 (2022).

    Google Scholar 

  70. Fan, W. et al. Arabidopsis PLANT U-BOX44 down-regulates osmotic stress signaling by mediating Ca2+-DEPENDENT PROTEIN KINASE4 degradation. Plant Cell 35, 3870–3888 (2023).

    Google Scholar 

  71. Xu, X. et al. Convergence of light and chloroplast signals for de-etiolation through ABI4-HY5 and COP1. Nat. Plants 2, 16066 (2016).

    Google Scholar 

  72. O’Malley Ronan, C. et al. Cistrome and epicistrome features shape the regulatory DNA landscape. Cell 165, 1280–1292 (2016).

    Google Scholar 

  73. Xu, H. et al. The JA-to-ABA signaling relay promotes lignin deposition for wound healing in Arabidopsis. Mol. Plant 17, 1594–1605 (2024).

    Google Scholar 

  74. Park, Y. J., Lee, H. J., Ha, J. H., Kim, J. Y. & Park, C. M. COP1 conveys warm temperature information to hypocotyl thermomorphogenesis. N. Phytol. 215, 269–280 (2017).

    Google Scholar 

Download references

Acknowledgements

We thank Dr. Daoxin Xie (Tsinghua University) for providing coi1-8 seeds, Dr. Chuanyou Li (Shandong Agricultural University) for providing 35S:MYC2-Myc seeds, and Dr. Lei Wang (Institute of Botany, Chinese Academy of Sciences) for providing myc2-2 and myc2/3/4 seeds. This work was supported by grants from the Key Research and Development Program of Zhejiang Province (2024SSYS0100 to R.L.), National Key Research and Development Program of China (2024YFA1306702 to J.H.), National Natural Science Foundation of China (U25A20633 to R.L., 32270262 to J.H.), and Project of Stable Support for Youth Teams in Basic Research of the Chinese Academy of Sciences (YSBR-119 to J.H.).

Author information

Author notes
  1. These authors contributed equally: Peipei Qi, Junling Huai.

Authors and Affiliations

  1. State Key Laboratory of Forage Breeding-by-Design and Utilization, Key Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing, China

    Peipei Qi, Junling Huai, Nan Gao, Yuanyuan Yao & Rongcheng Lin

  2. Biotechnology Institute, Xianghu Laboratory, Hangzhou, China

    Peipei Qi & Rongcheng Lin

  3. University of Chinese Academy of Sciences, Beijing, China

    Junling Huai & Yuanyuan Yao

Authors
  1. Peipei Qi
    View author publications

    Search author on:PubMed Google Scholar

  2. Junling Huai
    View author publications

    Search author on:PubMed Google Scholar

  3. Nan Gao
    View author publications

    Search author on:PubMed Google Scholar

  4. Yuanyuan Yao
    View author publications

    Search author on:PubMed Google Scholar

  5. Rongcheng Lin
    View author publications

    Search author on:PubMed Google Scholar

Contributions

P.Q. performed most of the experiments, analyzed data, and wrote the manuscript; J.H. generated plant materials, analyzed data, discussed the project, and wrote the manuscript; N.G. and Y.Y. conducted part of experiments and material preparation; R.L. conceived and supervised the study, analyzed data, and revised the paper.

Corresponding authors

Correspondence to Junling Huai or Rongcheng Lin.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review

Peer review information

Nature Communications thanks Gen-ichiro Arimura and the other anonymous, reviewer(s) for their contribution to the peer review of this work. A peer review file is available.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary information (download PDF )

Descriptions of Additional Supplementary Files (download PDF )

Supplementary Data 1 (download XLSX )

Supplementary Data 2 (download XLSX )

Supplementary Data 3 (download XLSX )

Supplementary Data 4 (download XLSX )

Supplementary Data 5 (download XLSX )

Supplementary Data 6 (download XLSX )

Supplementary Data 7 (download XLSX )

Supplementary Data 8 (download XLSX )

Supplementary Data 9 (download XLSX )

Supplementary Data 10 (download XLSX )

Reporting Summary (download PDF )

Transparent Peer Review file (download PDF )

Source data

Source data (download XLSX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Qi, P., Huai, J., Gao, N. et al. Phytochrome B integrates jasmonic acid and warm temperature signaling pathways to regulate cotyledon chloroplast development. Nat Commun (2026). https://doi.org/10.1038/s41467-026-70131-w

Download citation

  • Received: 28 July 2025

  • Accepted: 19 February 2026

  • Published: 09 March 2026

  • DOI: https://doi.org/10.1038/s41467-026-70131-w

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Download PDF

Associated content

Collection

Light Signaling in Plants

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Videos
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • Aims & Scope
  • Editors
  • Journal Information
  • Open Access Fees and Funding
  • Calls for Papers
  • Editorial Values Statement
  • Journal Metrics
  • Editors' Highlights
  • Contact
  • Editorial policies
  • Top Articles

Publish with us

  • For authors
  • For Reviewers
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Nature Communications (Nat Commun)

ISSN 2041-1723 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing