Resistance to Salinity and Water Scarcity in Higher Plants. Insights from Extremophiles and Stress-Adapted Plants: Tools, Discoveries and Future Prospects

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Cover image for research topic "Resistance to Salinity and Water Scarcity in Higher Plants.  Insights from Extremophiles and Stress-Adapted Plants:  Tools, Discoveries and Future Prospects"
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Drought will reduce global crop production by >10% in 2050 substantially worsening global malnutrition. Breeding for resistance to drought will require accessing crop genetic diversity found in the wild accessions from the driest high stress ecosystems. Genome–environment associations (GEA) in crop wild relatives reveal natural adaptation, and therefore can be used to identify adaptive variation. We explored this approach in the food crop Phaseolus vulgaris L., characterizing 86 geo-referenced wild accessions using genotyping by sequencing (GBS) to discover single nucleotide polymorphisms (SNPs). The wild beans represented Mesoamerica, Guatemala, Colombia, Ecuador/Northern Peru and Andean groupings. We found high polymorphism with a total of 22,845 SNPs across the 86 accessions that confirmed genetic relationships for the groups. As a second objective, we quantified allelic associations with a bioclimatic-based drought index using 10 different statistical models that accounted for population structure. Based on the optimum model, 115 SNPs in 90 regions, widespread in all 11 common bean chromosomes, were associated with the bioclimatic-based drought index. A gene coding for an ankyrin repeat-containing protein and a phototropic-responsive NPH3 gene were identified as potential candidates. Genomic windows of 1 Mb containing associated SNPs had more positive Tajima’s D scores than windows without associated markers. This indicates that adaptation to drought, as estimated by bioclimatic variables, has been under natural divergent selection, suggesting that drought tolerance may be favorable under dry conditions but harmful in humid conditions. Our work exemplifies that genomic signatures of adaptation are useful for germplasm characterization, potentially enhancing future marker-assisted selection and crop improvement.

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Original Research
12 February 2018
Dynamics of stress-driven IR in mRNA encoding poplar ovarian cancer related transcription factor (ptOCR2-L, POTRI.002G102500). This example illustrates that stress-induced increase in copy number of the fully spliced ptocr-lptocr-lptocr2-l mRNA occurs concomitantly with a decrease in the relative ratios of both retained introns. (A) RNA-Seq coverage of ptocr-lptocr-lptocr2-l locus and design of splice junction (SJ)-specific primers. Primers designated as “Spliced” detect only the isoform with fully spliced introns 4 and 5 (gene model POTRI.002G102500.1); “I4R” – intron 4 is retained whereas intron 5 is spliced (reverse primer spans I4 SJ); “IR5” – I5 is retained whereas I4 is spliced (corresponds to gene model.3; forward primer spans I4 SJ). Stars indicate Cufflinks transcript assemblies supporting retention of both fourth and fifth introns (I4R + I5R) under the heat stress in roots and the fifth intron (I5R) in xylem. Y-axis indicates the number of Illumina reads aligned to the genome. (B) Gene model and differentially retained introns of ptOCR2-L transcripts. (C–E) Quantification of mRNA absolute copy number and relative ratios of the differentially retained introns vs. fully spliced transcripts in tissues under various stress treatments. Absolute copy number of mRNA was quantified using reverse transcription – droplet digital PCR (RT-ddPCR) and event-specific primers as described in Section “Materials and Methods.”
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Salt tolerance evaluation of introgression line DJ15. (A) Germination rate of rice seeds after treatment at 0, 100, and 150 mM NaCl for 3 days at 35°C. (B) Survival rate of 10-day-old seedlings after treatment at 0, 100, and 150 mM for 10 days and subsequent recovery for 7 days. (C–H) Field performance of rice under non-stress field conditions (ECe = 1.3 dS m−1, pH 7.01) and under salt-stress field conditions (ECe = 5.7 dS m−1, pH 8.45). *Indicates significant difference at P < 0.05 in Tukey's multiple comparisons test after ANOVA; **Indicates significant difference at P < 0.01 in Tukey's multiple comparisons test after ANOVA.
Original Research
17 January 2018
Improvement of Salt Tolerance Using Wild Rice Genes
Ruidang Quan
8 more and 
Rongfeng Huang

Salt stress causes significant reductions in rice production worldwide; thus, improving salt tolerance is a promising approach to meet the increasing food demand. Wild rice germplasm is considered a valuable genetic resource for improving rice cultivars. However, information regarding the improvement of salt tolerance in cultivated rice using wild rice genes is limited. In this study, we identified a salt-tolerant line Dongxiang/Ningjing 15 (DJ15) under salt-stress field conditions from the population of a salt tolerant Dongxiang wild rice × a cultivated rice variety Ningjing16 (NJ16). Genomic resequencing analysis of NJ16, DJ15 and Dongxiang wild rice revealed that the introgressed genomic fragments were unevenly distributed over the 12 chromosomes (Chr.) and mainly identified on Chr. 6, 7, 10, and 11. Using quantitative trait locus (QTL) mapping, we found 9 QTL for salt tolerance (qST) at the seedling stage located on Chr. 1, 3, 4, 5, 6, 8, and 10. In addition, sequence variant analysis within the QTL regions demonstrated that SKC1/HKT8/HKT1;5 and HAK6 transporters along with numerous transcriptional factors were the candidate genes for the salt tolerant QTL. The DJ15/Koshihikari recombinant inbred lines that contained both qST1.2 and qST6, two QTL with the highest effect for salt tolerance, were more tolerant than the parental lines under salt-stress field conditions. Furthermore, the qST6 near-isogenic lines with IR29 background were more tolerant than IR29, indicating that qST1.2 and qST6 could improve salt tolerance in rice. Overall, our study indicates that wild rice genes could markedly improve the salt tolerance of cultivated rice.

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