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.

  • Article
  • Published:

Forecasting rice latitude adaptation through a daylength-sensing-based environment adaptation simulator

Abstract

Global climate change necessitates crop varieties with good environmental adaptability. As a proxy for climate adaptation, crop breeders could select for adaptability to different latitudes, but the lengthy procedures for that slow development. Here, we combined molecular technologies with a streamlined in-house screening method to facilitate rapid selection for latitude adaptation. We established the daylength-sensing-based environment adaptation simulator (DEAS) to assess rice latitude adaptation status via the transcriptional dynamics of florigen genes at different latitudes. The DEAS predicted the florigen expression profiles in rice varieties with high accuracy. Furthermore, the DEAS showed potential for application in different crops. Incorporating the DEAS into conventional breeding programmes would help to develop cultivars for climate adaptation.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Allele information of photoperiodic genes in indica hybrid rice varieties.
Fig. 2: Number of Hd1 and DTH8 allelic combinations within combined ecological classes.
Fig. 3: Using DEAS step 1 to detect rice daylength-sensing processes.
Fig. 4: DEAS step 2 couples environmental adaptation and daylength sensing.
Fig. 5: Categorical manner for evaluating the DEAS inference accuracy.
Fig. 6: Evaluation of the DEAS inference accuracy using field data.
Fig. 7: Application of the DEAS to soybean.
Fig. 8: Working model for how daylength sensing mediates rice latitude adaptation.

Similar content being viewed by others

Data availability

Information about indica hybrid rice varieties grown in East Asia, including days to heading and geographic distribution, was obtained from the China Rice Data Center (http://www.ricedata.cn/). Daylength data for different latitudes were collected using the Rise and Set Times app developed by S. Vdovenko (http://www.lifewaresolutions.com/). The haplotype information of flowering-time genes for sterile and restorer lines can be obtained from MBKBASE (http://www.mbkbase.org)33. Hd3a and RFT1 expression data for a rice paddy field at Tsukuba, Japan, grown under normal agricultural conditions can be obtained from https://ricexpro.dna.affrc.go.jp/category-select.php47.

Code availability

In this study, we did not generate any custom code. All mathematical algorithms can be implemented through MATLAB (MathWorks; licence of Xiamen University) and R. All maps were drawn using libraries mapdata, maptools and ggplot2 in R software.

References

  1. Sloat, L. L. et al. Climate adaptation by crop migration. Nat. Commun. 11, 1243 (2020).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  2. Rosenzweig, C. et al. Assessing agricultural risks of climate change in the 21st century in a global gridded crop model intercomparison. Proc. Natl Acad. Sci. USA 111, 3268–3273 (2014).

    Article  ADS  CAS  PubMed  Google Scholar 

  3. Teixeira, J. E. et al. Hallauer’s Tuson: a decade of selection for tropical-to-temperate phenological adaptation in maize. Heredity 114, 229–240 (2015).

    Article  CAS  PubMed  Google Scholar 

  4. Eshed, Y. & Lippman, Z. B. Revolutions in agriculture chart a course for targeted breeding of old and new crops. Science 366, eaax0025 (2019).

    Article  CAS  PubMed  Google Scholar 

  5. Kloosterman, B. et al. Naturally occurring allele diversity allows potato cultivation in northern latitudes. Nature 495, 246–250 (2013).

    Article  ADS  CAS  PubMed  Google Scholar 

  6. Lu, S. et al. Natural variation at the soybean J locus improves adaptation to the tropics and enhances yield. Nat. Genet. 49, 773–779 (2017).

    Article  CAS  PubMed  Google Scholar 

  7. Lu, S. et al. Stepwise selection on homeologous PRR genes controlling flowering and maturity during soybean domestication. Nat. Genet. 52, 428–436 (2020).

    Article  CAS  PubMed  Google Scholar 

  8. Guo, L. et al. Stepwise cis-regulatory changes in ZCN8 contribute to maize flowering-time adaptation. Curr. Biol. 28, 3005–3015 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Hung, H. Y. et al. ZmCCT and the genetic basis of day-length adaptation underlying the postdomestication spread of maize. Proc. Natl Acad. Sci USA 109, E1913–E1921 (2012).

    Article  CAS  PubMed  Google Scholar 

  10. Yang, Q. et al. CACTA-like transposable element in ZmCCT attenuated photoperiod sensitivity and accelerated the postdomestication spread of maize. Proc. Natl Acad. Sci. USA 110, 16969–16974 (2013).

    Article  ADS  CAS  PubMed  Google Scholar 

  11. Zhang, J. et al. Combinations of the Ghd7, Ghd8 and Hd1 genes largely define the ecogeographical adaptation and yield potential of cultivated rice. New Phytol. 208, 1056–1066 (2015).

    Article  CAS  PubMed  Google Scholar 

  12. Gao, H. et al. Days to heading 7, a major quantitative locus determining photoperiod sensitivity and regional adaptation in rice. Proc. Natl Acad. Sci. USA 111, 16337–16342 (2014).

    Article  ADS  CAS  PubMed  Google Scholar 

  13. Yan, W. et al. Natural variation in Ghd7.1 plays an important role in grain yield and adaptation in rice. Cell Res. 23, 969–971 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Koo, B. H. et al. Natural variation in OsPRR37 regulates heading date and contributes to rice cultivation at a wide range of latitudes. Mol. Plant 6, 1877–1888 (2013).

    Article  CAS  PubMed  Google Scholar 

  15. Dai, X. et al. LHD1, an allele of DTH8/Ghd8, controls late heading date in common wild rice (Oryza rufipogon). J. Integr. Plant Biol. 54, 790–799 (2012).

    Article  CAS  PubMed  Google Scholar 

  16. Yan, W. H. et al. A major QTL, Ghd8, plays pleiotropic roles in regulating grain productivity, plant height, and heading date in rice. Mol. Plant 4, 319–330 (2011).

    Article  CAS  PubMed  Google Scholar 

  17. Xue, W. et al. Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice. Nat. Genet. 40, 761–767 (2008).

    Article  CAS  PubMed  Google Scholar 

  18. Zhang, Z. et al. Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions. Sci. Rep. 7, 5388 (2017).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  19. Du, A. et al. The DTH8-Hd1 module mediates day-length-dependent regulation of rice flowering. Mol. Plant 10, 948–961 (2017).

    Article  CAS  PubMed  Google Scholar 

  20. Nemoto, Y., Nonoue, Y., Yano, M. & Izawa, T. Hd1, a CONSTANS ortholog in rice, functions as an Ehd1 repressor through interaction with monocot-specific CCT-domain protein Ghd7. Plant J. 86, 221–233 (2016).

    Article  CAS  PubMed  Google Scholar 

  21. Zhu, S. et al. The OsHAPL1-DTH8-Hd1 complex functions as the transcription regulator to repress heading date in rice. J. Exp. Bot. 68, 553–568 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Goretti, D. et al. Transcriptional and post-transcriptional mechanisms limit Heading Date 1 (Hd1) function to adapt rice to high latitudes. PLoS Genet. 13, e1006530 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  23. Yano, M. et al. Hd1, a major photoperiod sensitivity quantitative trait locus in rice, is closely related to the Arabidopsis flowering time gene CONSTANS. Plant Cell 12, 2473–2484 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Wei, X. et al. DTH8 suppresses flowering in rice, influencing plant height and yield potential simultaneously. Plant Physiol. 153, 1747–1758 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Itoh, H. & Izawa, T. The coincidence of critical day length recognition for florigen gene expression and floral transition under long-day conditions in rice. Mol. Plant 6, 635–649 (2013).

    Article  CAS  PubMed  Google Scholar 

  26. Simpson, G. G. & Dean, C. Arabidopsis, the Rosetta stone of flowering time? Science 296, 285–289 (2002).

    Article  ADS  CAS  PubMed  Google Scholar 

  27. Salazar, J. D. et al. Prediction of photoperiodic regulators from quantitative gene circuit models. Cell 139, 1170–1179 (2009).

    Article  CAS  PubMed  Google Scholar 

  28. Sawa, M., Nusinow, D. A., Kay, S. A. & Imaizumi, T. FKF1 and GIGANTEA complex formation is required for day-length measurement in Arabidopsis. Science 318, 261–265 (2007).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  29. Osugi, A., Itoh, H., Ikeda-Kawakatsu, K., Takano, M. & Izawa, T. Molecular dissection of the roles of phytochrome in photoperiodic flowering in rice. Plant Physiol. 157, 1128–1137 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Itoh, H., Nonoue, Y., Yano, M. & Izawa, T. A pair of floral regulators sets critical day length for Hd3a florigen expression in rice. Nat. Genet. 42, 635–638 (2010).

    Article  CAS  PubMed  Google Scholar 

  31. Vince-Prue, D. Photoperiodism in Plants (McGraw-Hill, 1975).

  32. Cheng, S. H., Zhuang, J. Y., Fan, Y. Y., Du, J. H. & Cao, L. Y. Progress in research and development on hybrid rice: a super-domesticate in China. Ann. Bot. 100, 959–966 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  33. Li, X. et al. Analysis of genetic architecture and favorable allele usage of agronomic traits in a large collection of Chinese rice accessions. Sci. China Life Sci. 63, 1688–1702 (2020).

    Article  PubMed  Google Scholar 

  34. Wu, W. et al. Association of functional nucleotide polymorphisms at DTH2 with the northward expansion of rice cultivation in Asia. Proc. Natl Acad. Sci. USA 110, 2775–2780 (2013).

    Article  ADS  CAS  PubMed  Google Scholar 

  35. Kojima, S. et al. Hd3a, a rice ortholog of the Arabidopsis FT gene, promotes transition to flowering downstream of Hd1 under short-day conditions. Plant Cell Physiol. 43, 1096–1105 (2002).

    Article  CAS  PubMed  Google Scholar 

  36. Izawa, T. et al. Phytochrome mediates the external light signal to repress FT orthologs in photoperiodic flowering of rice. Genes Dev. 16, 2006–2020 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Takahashi, Y., Shomura, A., Sasaki, T. & Yano, M. Hd6, a rice quantitative trait locus involved in photoperiod sensitivity, encodes the α subunit of protein kinase CK2. Proc. Natl Acad. Sci. USA 98, 7922–7927 (2001).

    Article  ADS  CAS  PubMed  Google Scholar 

  38. Doi, K. et al. Ehd1, a B-type response regulator in rice, confers short-day promotion of flowering and controls FT-like gene expression independently of Hd1. Genes Dev. 18, 926–936 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Hori, K. et al. Hd16, a gene for casein kinase I, is involved in the control of rice flowering time by modulating the day-length response. Plant J. 76, 36–46 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Matsubara, K. et al. Natural variation in Hd17, a homolog of Arabidopsis ELF3 that is involved in rice photoperiodic flowering. Plant Cell Physiol. 53, 709–716 (2012).

    Article  CAS  PubMed  Google Scholar 

  41. Saito, H. et al. Ef7 encodes an ELF3-like protein and promotes rice flowering by negatively regulating the floral repressor gene Ghd7 under both short- and long-day conditions. Plant Cell Physiol. 53, 717–728 (2012).

    Article  CAS  PubMed  Google Scholar 

  42. Yang, Y., Peng, Q., Chen, G. X., Li, X. H. & Wu, C. Y. OsELF3 is involved in circadian clock regulation for promoting flowering under long-day conditions in rice. Mol. Plant 6, 202–215 (2013).

    Article  CAS  PubMed  Google Scholar 

  43. Zhao, J. et al. OsELF3-1, an ortholog of ARABIDOPSIS EARLY FLOWERING 3, regulates rice circadian rhythm and photoperiodic flowering. PLoS ONE 7, e43705 (2012).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  44. Shibaya, T. et al. Hd18, encoding histone acetylase related to Arabidopsis FLOWERING LOCUS D, is involved in the control of flowering time in rice. Plant Cell Physiol. 57, 1828–1838 (2016).

    Article  CAS  PubMed  Google Scholar 

  45. Zhang, B. et al. Genetic interactions among Ghd7, Ghd8, OsPRR37 and Hd1 contribute to large variation in heading date in rice. Rice 12, 48 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  46. Wang, P., Gong, R., Yang, Y. & Yu, S. Ghd8 controls rice photoperiod sensitivity by forming a complex that interacts with Ghd7. BMC Plant Biol. 19, 462 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  47. Nagano, A. J. et al. Deciphering and prediction of transcriptome dynamics under fluctuating field conditions. Cell 151, 1358–1369 (2012).

    Article  CAS  PubMed  Google Scholar 

  48. Jaeger, P. A., Doherty, C. & Ideker, T. Modeling transcriptome dynamics in a complex world. Cell 151, 1161–1162 (2012).

    Article  CAS  PubMed  Google Scholar 

  49. Araki, M. G., Gyokusen, K. & Kajimoto, T. Vertical and seasonal variations in temperature responses of leaf respiration in a Chamaecyparis obtusa canopy. Tree Physiol. 37, 1269–1284 (2017).

    Article  CAS  PubMed  Google Scholar 

  50. Hu, Y. N. et al. Rice production and climate change in northeast China: evidence of adaptation through land use shifts. Environ. Res. Lett. 14, 024014 (2019).

    Article  ADS  Google Scholar 

  51. Lv, Z. F. et al. Climate change impacts on regional rice production in China. Clim. Change 147, 523–537 (2018).

    Article  ADS  Google Scholar 

  52. Liu, Z. H. et al. Shifts in the extent and location of rice cropping areas match the climate change pattern in China during 1980-2010. Reg. Environ. Change 15, 919–929 (2015).

    Article  Google Scholar 

  53. Li, Z. G. et al. Chinese rice production area adaptations to climate changes, 1949-2010. Environ. Sci. Technol. 49, 2032–2037 (2015).

    Article  ADS  CAS  PubMed  Google Scholar 

  54. 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).

    Article  CAS  PubMed  Google Scholar 

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

    Article  ADS  CAS  PubMed  Google Scholar 

  56. Ma, X. et al. A robust CRISPR/Cas9 system for convenient, high-efficiency multiplex genome editing in monocot and dicot plants. Mol Plant 8, 1274–1284 (2015).

    Article  CAS  PubMed  Google Scholar 

  57. Naito, Y., Hino, K., Bono, H. & Ui-Tei, K. CRISPRdirect: software for designing CRISPR/Cas guide RNA with reduced off-target sites. Bioinformatics 31, 1120–1123 (2015).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by the National Key R&D Program of China (2017YFA0506100), the National Natural Science Foundation (31671378) and the Fundamental Research Funds for the Central Universities (20720170068 and 20720190085). We thank Y. Liu (South China Agricultural University) for providing the pYLCRISPR/Cas9-MTmono vectors. We thank the breeder L. Wang (Sichuan Agricultural University) for providing the indica hybrid rice seeds. We thank X. Wang Deng (Peking University), H. Wang (South China Agricultural University) and F. Kong (Guangzhou University) for reading and commenting on the manuscript. We thank Y. Cui (Xiamen University), Z. Zeng (Sichuan Agricultural University), Y. Wang (Sichuan Agricultural University), W. Hu (Xiamen University) and X. Liu (Xiamen University) for their technical assistance.

Author information

Authors and Affiliations

Authors

Contributions

X.O. designed the research; L.Q., Q.W., X.W., G.Z., Z.S., J.H., H.W., W.T., Q.L., J.R., J.X., C.L., Y.L., S.L., R.H., X.C., C.Z., M.L., X.H., S.L. and X.O. performed the research; L.Q., P.Q., Z.C., Z.L., H.H., J.H., X.W., C.L. and X.O. analysed the data; X.O. wrote the paper.

Corresponding author

Correspondence to Xinhao Ouyang.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information Nature Food thanks the anonymous reviewers for their contribution to the peer review of this work.

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

Supplementary information

Supplementary Information

Supplementary Figs. 1–25, and Tables 1 and 2.

Reporting Summary

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Qiu, L., Wu, Q., Wang, X. et al. Forecasting rice latitude adaptation through a daylength-sensing-based environment adaptation simulator. Nat Food 2, 348–362 (2021). https://doi.org/10.1038/s43016-021-00280-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s43016-021-00280-2

Search

Quick links

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research