Yang Zhu
Zhong-Hua Chen
Maximiller Dal-Biaco
Shuijin Hua- 1Institute of Crop Science, Zhejiang University, Hangzhou, China
- 2School of Science, Western Sydney University, Penrith, NSW, Australia
- 3Departamento de Bioquímica, Universidade Federalde Viçosa, Viçosa, Minas Gerais, Brazil
- 4Institute of Crop and Nuclear Technology Utilization, Zhejiang Academy of Agricultural Sciences, Hangzhou, China
Editorial on the Research Topic
Genetics, evolution, and utilization of germplasm in crop improvement
Genetic diversity of different plant species is fundamental for trait development (Chung et al., 2023). By using either advanced sequencing or mutagenesis, knowledge of genetic diversity has been enriched in five newly published studies of Prunus tenella, Lagerstroemia indica, Pisum sativum, Polygonati odorati and Ipomoea batatas. Each study focused on specific genetic aspects, such as the P. tenella mitochondrial genome structure and unique gene transfer patterns, L. indica chloroplast genome emphasizing photosynthesis gene evolution and boundary shifts, and P. sativum SNP-based diversity highlighting population structure in landraces and cultivars. Together, these studies reveal phylogenetic relationships and adaptive traits, which could further support targeted breeding, conservation, and improved resilience in agricultural contexts. These findings collectively enrich genetic resources for many critical plant species.
Newly characterized levels and patterns of genetic diversity are critical for plant identification and feature specifications. There are three papers from different Chinese groups in this issue using genetic information from the cytoplasm, such as mitochondrial or chloroplast DNA evidence to distinguish plant genomic features. For example, in-depth analysis of the mitochondrial genome of the Chinese wild dwarf almond P. tenella, a rare and valuable plant with medicinal and ornamental potential, complements the chromosome level genome assembly (Qin et al., 2023). Using advanced Illumina and Oxford Nanopore sequencing platforms, the assembled mitochondrial genome of 452,158 bp in length contains 63 unique genes, comprising 36 protein-coding genes, 24 tRNA genes, and 3 rRNA genes (Liu et al.). However, differing from some other Prunus species, P. tenella exhibits unique repeat sequences, RNA editing sites, and intergenomic gene transfers between mitochondria and chloroplasts. Phylogenetic analysis places P. tenella closely with Rosaceae family members but highlights distinctions in its evolutionary pathway compared to Prunus dulcis, indicating divergent adaptation strategies within the genus.
By using the chloroplast genome structure of Lagerstroemia indica “Pink Velour” and six related species, intricate mechanisms of photosynthesis gene evolution have been revealed (He et al.). The high-resolution genome assembly contains 152,174 bp with a detailed annotation of 85 protein-coding genes, 37 tRNAs, and 8 rRNAs. Authors uncovered unique boundary variations in the ycf1 gene across species, an evolutionary feature that distinguishes species like Lagerstroemia fauriei and Lagerstroemia limii. Another notable contribution is the use of nonsynonymous substitution rates (Ka/Ks) in photosynthesis genes, showing variation in L. fauriei, L. limii, and Lagerstroemia subcostata that indicate potential adaptive responses to differing climates (He et al.). Those findings are consistent with the previous study of divergence times of Lagerstroemia by using chloroplast phylogenomics of 35 species, which identified the ycf1 gene as being quite variable during evolution (Dong et al., 2021).
For the four medicinal Polygonatum species, using codon usage bias (CUB) to analyze the codon preferences of 204 chloroplast protein-coding genes (PCGs) found the chloroplast genomes with weak codon usage bias (Shi et al.). These plant chloroplast genomes are enriched for AT bases and AT-ending codons. Natural selection is the main factor influencing codon usage bias, and mutation pressure also plays a role (Shi et al.). This study is of importance to distinguish Polygonatum plants, among which more than 30 species have been globally used as traditional medicine and functional food because of many chemical constituents with verified biological activities (Zhao et al., 2018).
Toward improvement of agronomic traits, a population with natural genetic variation or generated mutagenesis pools is of great importance for breeding or pre-breeding programs (Holme et al., 2019). This Swedish group used 265 globally sourced accessions of pea (P. sativum), applying advanced Diversity Arrays Technology (DArT) sequencing to identify 6,966 SNP and 8,454 in silico markers (Brhane and Hammenhag). This highly informative genetic dataset exhibited the highest diversity (Ne = 1.52, He = 0.31), with unique private alleles primarily in European accessions (22 alleles), making these groups particularly valuable for future breeding (Brhane and Hammenhag). Notably, the reference genome of the elite vegetable pea cultivar “Zhewan No.1” has been recently released, providing genetic information relevant to many agronomic traits (Liu et al., 2024).
A Korean group chose to apply gamma radiation to the sweetpotato (I. batatas) cultivar “Tongchaeru” for genetic mutagenesis. With the aim of altered stem growth patterns, authors combined transcriptomic changes and genetic alterations for agronomic trait changes (Lee et al.). In summary, researchers identified notable phenotypic changes in stem morphology, such as longer or thinner stems in mutants compared to the wild type. Transcriptomic analysis detected 15,832 differentially expressed genes, with critical upregulation in the auxin-response gene SAUR and PIF4, a key gene for cell elongation (Lee et al.). This suggests that gamma-induced mutations can enhance auxin and gibberellin pathways, promoting stem elongation. Due to the highly heterozygous hexaploid genome of I. batatas, complicated genetic studies and breeding programs have been comprehensively reviewed for better sweetpotato improvement (Yan et al., 2022).
Author contributions
YZ: Writing–original draft, Writing–review and editing. Z-HC: Supervision, Writing–review and editing. MD-B: Supervision, Writing–review and editing. SH: Writing–review and editing.
Funding
The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by National Natural Science Foundation of China (32100274 and 32370353) and Young Elite Scientists Sponsorship Program by CAST (2020QNRC001).
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.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
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References
Chung, M. Y., Merilä, J., Li, J., Mao, K., López-Pujol, J., Tsumura, Y., et al. (2023). Neutral and adaptive genetic diversity in plants: an overview. Front. Ecol. Evol. 11, 1116814. doi:10.3389/fevo.2023.1116814
Dong, W., Xu, C., Liu, Y., Shi, J., Li, W., and Suo, Z. (2021). Chloroplast phylogenomics and divergence times of Lagerstroemia (Lythraceae). Bmc. Genomics 22, 434–34. doi:10.1186/s12864-021-07769-x
Holme, I. B., Gregersen, P. L., and Brinch-Pedersen, H. (2019). Induced genetic variation in Crop plants by random or targeted mutagenesis: convergence and differences. Front. Plant Sci. 10, 1468. doi:10.3389/fpls.2019.01468
Liu, N., Lyu, X., Zhang, X., Zhang, G., Zhang, Z., Guan, X., et al. (2024). Reference genome sequence and population genomic analysis of peas provide insights into the genetic basis of Mendelian and other agronomic traits. Nat. Genet. 56 (9), 1964–1974. doi:10.1038/s41588-024-01867-8
Qin, Y., Zhao, H., Han, H., Zhu, G., Wang, Z., and Li, F. (2023). Chromosome-level genome assembly and population genomic analyses reveal geographic variation and population genetic structure of Prunus tenella. Int. J. Mol. Sci. 24, 11735. doi:10.3390/ijms241411735
Yan, M., Nie, H., Wang, Y., Wang, X., Jarret, R., Zhao, J., et al. (2022). Exploring and exploiting genetics and genomics for sweetpotato improvement: status and perspectives. Plant Commun. 3 (5), 100332. doi:10.1016/j.xplc.2022.100332
Keywords: genetics, evolution, germplasm, crop improvement, advanced technologies
Citation: Zhu Y, Chen Z-H, Dal-Biaco M and Hua S (2024) Editorial: Genetics, evolution, and utilization of germplasm in crop improvement. Front. Genet. 15:1527639. doi: 10.3389/fgene.2024.1527639
Received: 13 November 2024; Accepted: 05 December 2024;
Published: 16 December 2024.
Edited and reviewed by:
Andrew H. Paterson, University of Georgia, United StatesCopyright © 2024 Zhu, Chen, Dal-Biaco and Hua. 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: Yang Zhu, emh1eWFuZzIwMjBAemp1LmVkdS5jbg==; Shuijin Hua, c2podWExQDE2My5jb20=