Skip to main content

EDITORIAL article

Front. Plant Sci., 02 June 2023
Sec. Functional and Applied Plant Genomics
This article is part of the Research Topic Genomics and Phenomics of Crop Wild Relatives (CWRs) For Crop Improvement View all 7 articles

Editorial: Genomics and phenomics of crop wild relatives (CWRs) for crop improvement

  • 1Division of Genomic Resources, Indian Council of Agricultural Research (ICAR)-National Bureau of Plant Genetic Resources, New Delhi, India
  • 2Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, St Lucia, QLD, Australia
  • 3Indian Council of Agricultural Research (ICAR)-National Bureau of Plant Genetic Resources (NBPGR)-Regional Station, Thrissur, India
  • 4Department of Botany, Faculty of Science, Palacký University, Olomouc, Czechia

Crop wild relatives (CWRs) exhibit a close relationship with domesticated crops (agri-horticultural, medicinal and aromatic, ornamental, and forestry species) and form a part of the crop’s gene pool with potential for gene exchange. A large number of CWRs are potential donors but receive less attention than domesticated crops. CWRs have also suffered from genetic erosion resulting in a severe loss of genetic diversity (Maxted et al., 2006; von Wettberg et al., 2020). The factors that drive this loss in genetic diversity have been categorized into remote drivers and proximate drivers that act on the evolutionary forces: mutation, migration/gene flow, genetic drift, and selection (Khoury et al., 2022).

In this Research Topic, Trainin et al. documented from an anatomical perspective, the evolutionary forces involved in the selection of the non-foliar photosynthesis trait in the stems of Prunus arabica (Olivier) Meikle (a CWR of almond) when compared to the commercial almond (P. dulcis (Mill.) D. A. Webb). The stems of P. arabica favor stem photosynthesis for additional carbon gain through multiple strategies. Higher stem photosynthesis in P. arabica than in P. dulcis is attributed to selective anatomical features such as the presence of a high density of sunken stomata in their stems, a chloroplast-rich mesophyll-like parenchymatous cell layer, higher chlorophyll content, better chlorophyll fluorescence and quenching parameters, and its ability to efficiently regulate water loss at elevated temperatures.

Zhu et al. identified the molecular mechanism of an R2R3-MYB transcription factor gene underlying a drought tolerance trait, VyMYB24, isolated from a drought-tolerant grapevine wild relative– Vitis yanshanesis J. X. Chen. This gene was identified as a nuclear protein that was significantly upregulated during drought to impart drought stress tolerance and functionally validated through the genetic transformation of tobacco. Transgenic plants overexpressing the VyMYB24 gene were phenotypically dwarfed with a lower leaf area, reduced flower size, and seed weight. The role of VyMYB24 in regulating the gibberellin biosynthetic pathway was studied.

Du et al. reported the introgression of stripe rust and Fusarium head blight resistance genes from Leymus mollis (Trin.) Pilg. (2n = 4x = 28, NsNsXmXm) into wheat cv. 7182 through an alien disomic substitution line, M862 (2n = 6x = 42, 21II), using an inter-specific octoploid hybrid Tritileymus (2n = 8x = 56, AABBDDNsNs or AABBDDXmXm). Cytogenetic studies indicate that the disomic substitution line (M862) carried 4Ns in place of 4D chromosomes. A few structural variations in chromosomes 1A, 1D, 2B, and 5A were also reported and the transcriptome analysis identified the genes and Ns-specific markers associated with resistance genes that had utility in wheat improvement programs.

With the availability of genomics tools, whole genome sequence information, and a reference set for the desired trait representing the complete range of trait variation, it is very possible to identify the candidate genes underlying the trait variation. Gowda et al. used a genome-wide association approach to mine the candidate genes associated with the straw silica content trait in the germplasm of the rice progenitor, Oryza nivara S.D.Sharma & Shastry, representing the variability of 5-16% silica content among a set of 258 accessions. This study led to the identification of the candidate genes, an ATP-binding cassette (ABC) transporter, casparian thickenings, multi-drug and toxin extrusion (MATE) protein, F-box, and MYB-transcription factors.

An understanding of the factors underlying genetic diversity loss will help identify ways to reverse genetic diversity losses and support the introgression of desirable traits into domesticated ones. Though gene introgression from wild to crops is possible, it is mostly untapped due to the deleterious effects of linkage drag reducing genetic gain and selection efficiency and, thus, gene introgression is considered to be the ‘cost of domestication’ (Moyers et al., 2018). Besides linkage drag, pulses and oilseeds do not yield higher genetic gain due to low variation. Hence, to create variation and thereby achieve acceptable genetic gain, mutation breeding has been the method of choice for these two crop groups in earlier decades. Singh et al. underscore the difficulties in achieving higher genetic gain with special reference to legume crops. Their research provides an overview of the key strategic approaches such as broadening the genetic base through alien introgression from CWRs. In addition, integration of the strategic approaches with modern tools, such as genetic engineering, genome editing, and speed breeding, along with present-day omics tools will potentially bring a paradigm shift in legume breeding programs to achieve higher genetic gain with minimal costs.

An understanding of the genomics of linkage drag (Huang et al., 2023) would help balance the domestication cost. Besides, CWRs play an important role in understanding crop geography and hence its origin, as proposed by Vavilov (1935). Barazani et al. discuss the history of olive cultivation using archaeological evidence that documented the presence of plant remains of wild olive, Olea europaea L. subsp. europaea var. sylvestris (Mill.) Lehr during the Middle Pleistocene (roughly 780,000 years ago) in the Southern Levant region. Selection pressure on this wild form gave rise to the present-day cultivated olives, Olea europaea subsp. europaea var. europaea. This warrants further genetic studies among the naturally grown olive populations with traditional landraces and modern cultivars to understand the loci being subjected to selection pressure in the domestication process. With the proven strength of genome editing tools in the creation of de novo domesticated crop plants in the CWRs of model crop plants such as rice and tomato (Li et al., 2018; Yu et al., 2021), a broader understanding of the CWRs in the -omics era will potentially help accelerate crop improvement.

Author contributions

Author PR wrote the first draft and all authors have contributed to finalize the manuscript. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Huang, K., Jahani, M., Gouzy, J., Legendre, A., Carrere, S., Lazaro-Guevara, J. M., et al. (2023). The genomics of linkage drag in inbred lines of sunflower. Proc. Natl. Acad. Sci. U.S.A. 120, e2205783119. doi: 10.1073/pnas.2205783119

PubMed Abstract | CrossRef Full Text | Google Scholar

Khoury, C. K., Brush, S., Costich, D. E., Curry, H. A., de Haan, S., Engels, J. M. M., et al. (2022). Crop genetic erosion: understanding and responding to loss of crop diversity. New Phytol. 233, 84–118. doi: 10.1111/nph.17733

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, T., Yang, X., Yu, Y., Si, X., Zhai, X., Zhang, H., et al. (2018). Domestication of wild tomato is accelerated by genome editing. Nat. Biotech. 36, 1160–1163. doi: 10.1038/nbt.4273

CrossRef Full Text | Google Scholar

Maxted, N., Ford-Lloyd-Ford, B. V., Jury, S., Kell, S., Scholten, M. (2006). Towards a definition of a crop wild relative. Biod. Conserv. 15, 2673–2685. doi: 10.1007/s10531-005-5409-6

CrossRef Full Text | Google Scholar

Moyers, B. T., Morrell, P. L., McKay, J. K. (2018). Genetic costs of domestication and improvement. J. Hered. 109, 103–116. doi: 10.1093/jhered/esx069

PubMed Abstract | CrossRef Full Text | Google Scholar

Vavilov, N. I. (1935). “Theoretical basis for plant breeding, vol. 1. origin and geography of cultivated plants,” in The phytogeographical basis for plant breeding. Ed. Love, D. (Cambridge, UK: Cambridge University Press), 316–366.

Google Scholar

von Wettberg, E., Davis, T. M., Smykal, P. (2020). Editorial: wild plants as source of new crops. Front. Plant Sci. 11. doi: 10.3389/fpls.2020.591554

CrossRef Full Text | Google Scholar

Yu, H., Lin, T., Meng, X., Du, H., Zhang, J., Liu, G., et al. (2021). A route to de novo domestication of wild allotetraploid rice. Cell 184, 1156–1170.e14. doi: 10.1016/j.cell.2021.01.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: crop wild relative (CWR), genomics, phenomics, domestication cost, candidate gene analysis, de novo domestication

Citation: Rangan P, Pradheep K, Archak S, Smýkal P and Henry R (2023) Editorial: Genomics and phenomics of crop wild relatives (CWRs) for crop improvement. Front. Plant Sci. 14:1221601. doi: 10.3389/fpls.2023.1221601

Received: 12 May 2023; Accepted: 25 May 2023;
Published: 02 June 2023.

Edited and Reviewed by:

Yi-Hong Wang, University of Louisiana at Lafayette, United States

Copyright © 2023 Rangan, Pradheep, Archak, Smýkal and Henry. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Parimalan Rangan, ci5wYXJpbWFsYW5AaWNhci5nb3YuaW4=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.