LAUSR

Fusarium head blight (FHB) is one of the devastating diseases for wheat production worldwide, which causes significant yield losses and reduces grain quality because of mycotoxins contamination in wheat grains. As wheat relatives, Thinopyrum elongatum and Th. ponticum are important genetic resources that can be used to improve wheat FHB resistance. Using recombinant inbred lines derived from a cross between two Thatcher-Th. ponticum substitution lines, K11463 (7E1/7D) and K2620 (7E2/7D), the major FHB resistance locus Fhb7 was mapped to the very distal region of the long arm of chromosome 7E2 (Guo et al., 2015). Wang et al. (2020) sequenced the genome of Th. elongatum and cloned the glutathione Stransferase-encoding Fhb7 by genetic mapping. Relying on the recombination between Th. elongatum chromosome 7E and Th. ponticum chromosome 7E1, a resistant gene Fhb-7EL for FHB resistance was located to the long arm of 7E (Ceoloni et al., 2017). To transfer the resistant gene Fhb-7EL to common wheat, hundreds of wheat-Th. elongatum translocation lines were developed by irradiating the pollen of the wheat-Th. elongatum addition line Chinese Spring (CS)-7EL at anthesis, among which Zhongke 1878 proved to carry an approximately 100 Mb 7EL chromatin on chromosome 6DL (Figure 1a, Figure S1, Appendix S1). After backcrossing Zhongke 1878 with the highly susceptible variety Jimai 22 for six generations, FHB resistance evaluation showed that the translocated chromosome could significantly increase the FHB resistance of Jimai 22 to the level of Sumai 3 by decreasing the number of diseased spikelets from 13.43 to 1.43 (Figure 1b,c). To explore the nature of the FHB resistance gene, we inoculated the spikes of the line Zhongke 1878 with F. graminearum and performed single-molecule real-time isoform sequencing after 96 h. Removing the transcripts derived from wheat and Fusarium species by blasting wheat reference genome and nucleotide database on NCBI, 25 transcripts were identified derived from alien chromatin by PCR in Zhongke 1878 (Figure S2, Tables S1 and S2). To study the mechanisms of FHB resistance in the line Zhongke 1878, next-generation sequencing-based transcriptomic analysis was performed on these 25 transcripts. Annotated as a GST protein, the expression of the transcript T26102 was significantly increased 48 h after inoculation with F. graminearum (Figure 1d,e, Table S1). To illustrate the association between T26102 and FHB resistance, the distribution of T26102 was checked in a series of wheat-Thinopyrum derivatives. The homologue of T26102 was not only detected in wheat-Th. ponticum amphiploid SNTE20 but also in the wheat-Th. ponticum translocation lines 4460 and 4462 (Figure 1f, Figures S3, S4). After sequencing the amplified product, two different T26102 homologues were discovered in lines CS-7EL, Zhongke 1878 and SNTE20 respectively (Figure 1f, Figure S4). Although SNTE20, 4460 and 4462 were proven to carry the GST-encoding Fhb7 homologues, all three lines were identified as susceptible to FHB as well as the susceptible control Jimai 22 (Figure 1g,h). Expression analysis revealed that Fhb7 homologues were induced in lines 4460, 4462 and SNTE20 after inoculating with F. graminearum (Figure 1i). Similar results were also reported in the wheat-Th. ponticum partial amphiploid SNTE122 and translocation line TNT-B (Guo et al., 2022). More puzzling was that the Fhb7 homologue and its promoter shared by 4460 and 4462 were identical to the one in the wheat-Th. ponticum substitution line 7E2/7D used as the resistant parent to map Fhb7 (Figure 1f, Figures S4, S5). All these results casted our doubt on the FHB-resistant function of the GSTs. To verify the FHB resistance function of T26102, we transformed the overexpression vector pUbi:T26102 into three common wheat accessions 19AS161, Jimai 22 and Zhongmai 175. The transgenic positive wheat plants overexpressing T26102 were used for FHB resistance evaluation (Figure S6). A few bleached spikelets were observed on all spikes of both wild types and T0 transgenic plants 7 days after inoculation with F. graminearum (Figure 1j). Statistical analysis was performed between the wild type and the transgenic plants; no difference was discovered between them (Figure 1k). To rule out the effect of amino acid variation on the function of T26102, we also