Category: Pub Med

G3 (Bethesda). 2026 Oct 10:jkag278. doi: 10.1093/g3journal/jkag278. Online ahead of print.

ABSTRACT

Southern stem canker (SSC), caused by Diaporthe aspalathi, is a major soybean disease causing yield losses of up to 80%. Genetic resistance is the most effective and sustainable strategy for managing SSC. “Tracy-M” is a cultivar with broad resistance to D. aspalathi isolates; however genomic location of the resistance is unknown. To determine the genetic basis of SSC resistance in Tracy-M and its derived progeny, two Tracy-M-derived lines, D85-10404 and D85-10412, were each crossed with a common susceptible parent, G81-2057, to develop recombinant inbred line (RIL) populations. Quantitative Trait Locus (QTL) sequencing (QTL-seq) and composite interval mapping (CIM) identified a common major QTL on chromosome (Chr) 2 in both lines corresponding to Rdm1 locus defined from a previous genetic study. Additionally, second QTL located on Chr 17 (Rdm2 locus) was only detected in the D85-10412-derived RIL population. To validate Tracy-M-derived resistance, an F2:3 population from G00-3213 × Tracy-M was developed. Bulked segregant analysis (BSA) and CIM identified a major QTL on Chr 14, overlapping the previously reported Rdm3 locus in “Crockett” and PI 398469, while Rdm1 was not detected, suggesting genetic background effects. Kompetitive allele-specific PCR (KASP) markers were developed to facilitate selection of Rdm1, Rdm2, and Rdm3 resistance alleles in soybean breeding programs.

PMID:42857980 | DOI:10.1093/g3journal/jkag278

bioRxiv [Preprint]. 2026 Sep 7:2026.09.03.748874. doi: 10.64898/2026.09.03.748874.

ABSTRACT

Plant-parasitic nematodes cause extensive crop losses that threaten global food security and create substantial economic hardship, yet strategies for their control remain limited. Although plant-parasitic nematodes have life cycles that mirror those of their free-living and animal-parasitic relatives, comparatively little is known about the signals that drive life-cycle progression. Dafachronic acids (DAs) are steroid hormones that control life cycle by activating DAF-12 nuclear receptors in Caenorhabditis elegans and animal-parasitic nematodes. To define whether an analogous pathway exists in plant-parasitic nematodes, we investigated the responsiveness of DAF-12 orthologs from six plant-parasitic nematode species to Δ7-DA, an endogenous DAF-12 ligand in C. elegans and several animal-parasitic nematodes. We find that whereas some plant-parasitic nematode receptors are activated by Δ7-DA, others are not. Structural modeling of all six ligand-binding domains, together with docking of Δ7-DA into each model, indicates that responsiveness is governed by a combinatorial ligand-recognition network surrounding the ligand carboxylate rather than by any single contact residue. We further demonstrate that egg and second-stage juvenile extracts from the soybean cyst nematode, Heterodera glycines, lack detectable DA but contain distinct lipophilic fractions that activate its DAF-12 ortholog. Together, these findings suggest that many plant-parasitic nematodes utilize endogenous DAF-12 ligands that are structurally distinct from DA. Uncovering modulators of this pathway could lead to new strategies to combat nematode-driven crop loss.

PMID:42818229 | PMC:PMC13622478 | DOI:10.64898/2026.09.03.748874

Appl Environ Microbiol. 2026 Oct 7:e0125726. doi: 10.1128/aem.01257-26. Online ahead of print.

ABSTRACT

Maize produces pre-formed secondary metabolites with antimicrobial and invertebrate anti-herbivory properties. Fusarium verticillioides, a mycotoxigenic maize pathogen, detoxifies the maize phytoanticipin 2-benzoxazolinone (BOA) through gene action of FvMBL1, which encodes a putative metallo-β-lactamase within the FDB1 gene cluster. This cluster is also present in other maize-colonizing fungi, including the pathogen Colletotrichum graminicola and, as reported here, the protective endophyte Sarocladium zeae, which exhibits antagonistic activity against mycotoxigenic fungi. The role of the FvMBL1 ortholog in S. zeae, designated SzMBL1, was assessed by gene deletion and add-back complementation. Deletion of SzMBL1 rendered S. zeae incapable of degrading BOA and therefore unable to grow on BOA-amended medium, whereas complemented add-back strains restored BOA tolerance and, in some cases, enhanced growth at higher concentrations of BOA. Quantitative PCR analyses revealed higher copy numbers and expression levels in all add-back transformants relative to the wild type, consistent with their enhanced growth. HPLC-MS/MS analysis further showed that SzMBL1 hydrolyzes BOA, ultimately resulting in biotransformation into the non-toxic metabolite N-(2-hydroxyphenyl)malonamic acid (HPMA). Together, this study confirms the conserved function of the SzMBL1 gene involved in BOA detoxification. This study suggests that the FDB1 gene cluster, harboring SzMBL1 in S. zeae, was likely transferred through horizontal gene transfer between maize-colonizing fungi and plays a role in the degradation of host-derived secondary metabolites that function as filters limiting which fungi are most frequently associated with maize.IMPORTANCEMaize produces secondary metabolites such as 2-benzoxazolinone (BOA) to help protect against microbes and insects. The pathogenic Fusarium verticillioides carries FvMBL1, a gene within the FDB1 gene cluster that helps break down BOA. This cluster is also present in other maize-associated fungi such as Colletotrichum graminicola and, as reported here, the protective fungus Sarocladium zeae. In our experiments, when a gene similar to FvMBL1, denoted SzMBL1, is deleted in S. zeae, the fungus could no longer break down BOA or grow on BOA-amended medium. Complementation restored BOA tolerance and growth phenotypes. Notably, some S. zeae add-back strains showed increased growth at higher BOA concentrations. Our analysis showed that these hypertolerant complemented strains had multiple, transcriptionally active copies of SzMBL1. The study highlights the role of SzMBL1 in BOA detoxification, thereby aiding fungal tolerance to antimicrobial compounds, and supports the hypothesis that the FDB1 gene cluster can be horizontally transferred among maize-colonizing fungi.

PMID:42841629 | DOI:10.1128/aem.01257-26

PLoS Genet. 2026 Oct 5;22(10):e1012327. doi: 10.1371/journal.pgen.1012327. Online ahead of print.

ABSTRACT

In animals, plants, and some fungi, Polycomb Repressive Complex 2 (PRC2) catalyzes trimethylation of histone H3 lysine 27 (H3K27me3) to establish transcriptionally repressed chromatin. Here, we identify the histone acetyltransferase RTT109 as a key regulator of PRC2-repressed domains in the model fungus Neurospora crassa. Although RTT109 interacts with the Vps75 homolog Nucleosome Assembly Factor 2 (NAF-2), we show that proper structure and function of PRC2-methylated chromatin require RTT109 catalytic activity but are independent of NAF-2 and H3K56 acetylation. We further demonstrate that H3K27me3 can be stably propagated over multiple rounds of mitosis in the absence of sequence-specific PRC2 targeting, and that RTT109 is essential for maintenance of the repressed state. These findings uncover a replication-linked mechanism for epigenetic memory and establish RTT109 as a key regulator of Polycomb-mediated chromatin inheritance.

PMID:42832562 | DOI:10.1371/journal.pgen.1012327

Proc Natl Acad Sci U S A. 2026 Oct 6;123(40):e2524371123. doi: 10.1073/pnas.2524371123. Epub 2026 Sep 29.

ABSTRACT

Many motile and sensory functions of cilia and flagella depend on the precise localization of transmembrane proteins within the ciliary membrane. Rather than being uniformly distributed, these proteins are often targeted to specific subciliary regions along the length or circumference of cilia. Here, we use genome editing and in vivo imaging to dissect the spatial organization of the channel protein PKD2 in Chlamydomonas cilia. MST3, a PKD2-like protein with five transmembrane helices (5TMH), is localized exclusively to the distal cilium, where it is essential for the localization of PKD2 and the formation of the hair-like mastigonemes. MST3, however, is dispensable for PKD2 assembly in the proximal cilium. In contrast, the PKD2-like 5TMH protein Proximal PKD2 Interactor (PPI) resides in the proximal cilium, where it is required for PKD2 assembly; ppi mutants retain distal PKD2 and mastigonemes. In mst3 ppi double knockouts, both proximal and distal PKD2 are absent, revealing that MST3 and PPI organize PKD2 into distal and proximal regions. Further, PKD2 colocalizes and comigrates with PKD2-like protein 1 (PLP1), another 5TMH protein, in cilia, indicating that they are present together in a complex. While plp1 mutants swim largely normally, mst3 and, to a lesser degree, ppi mutants swim with reduced velocity, indicating a functional specialization of the different ciliary PKD2 complexes. Thus, Chlamydomonas PKD2 associates with one of several 5TMH proteins to form spatially and genetically distinct PKD2 complexes, while also establishing their longitudinal distribution in cilia.

PMID:42809393 | DOI:10.1073/pnas.2524371123

G3 (Bethesda). 2026 Sep 28:jkag269. doi: 10.1093/g3journal/jkag269. Online ahead of print.

ABSTRACT

Polyploidization in peanut (Arachis hypogaea L.) fixed heterosis but also caused a genetic bottleneck isolating cultivated peanut from its wild diploid relatives. Mechanisms such as homoeologous exchange can partially restore genetic diversity by generating new allelic combinations. Double reduction is a rare polyploid-specific segregation pattern in which a single-dosage locus yields duplex gametes. It requires multivalent formation-associated with homoeologous exchange in allopolyploids-and crossing over between non-sister chromatids. Although peanut mainly exhibits disomic pairing, occasional multivalents theoretically allow low-frequency double reduction. To estimate double reduction and examine its relationship with genetic instability, we constructed a high-density phased linkage map (9,717 markers, 0.22 cM average spacing) from a backcross population between cultivated peanut and the neoallotetraploid [A. magna × A. stenosperma]4x (MagSten). Initial maps showed distinctive double linkage group artifacts, and some progenies displayed abnormal genotyping patterns linked to unbalanced chromosomal compositions, outcomes of homoeologous exchange. Removing these progenies resolved the artifacts, revealing a previously unrecognized mapping artifact in allotetraploid peanut and suggesting a common origin for similar artifacts observed in other linkage maps. Analysis of the phased map detected double reduction in 12% of progenies; one event was confirmed as producing a genomic composition matching theoretical predictions, supporting the hypothesis that double reduction causes unbalanced genomic compositions in allopolyploids as well. These results indicate that double reduction is a rare but recurrent phenomenon in segmental allotetraploid peanut that, together with homoeologous exchange, contributes to genetic instability and generates new allelic combinations in this and likely other allopolyploid genomes.

PMID:42802945 | DOI:10.1093/g3journal/jkag269

Phytopathology. 2026 Sep 26. doi: 10.1094/PHYTO-07-26-0235-R. Online ahead of print.

ABSTRACT

Fusarium head blight (FHB) is a destructive disease of wheat and barley caused by a complex of Fusarium species, including Fusarium poae. However, the transcriptional responses of F. poae during spike colonization remain insufficiently characterized. This study aimed to characterize and compare the temporal transcriptomic responses of F. poae during barley and wheat spike infection. We profiled the in planta transcriptome of F. poae isolate GA18W 5.2.4 in barley cv. Stander and wheat cv. SS8641 at 0, 24, 48, 72, and 96 h after inoculation (HAI). RNA sequencing, differential expression analysis, functional enrichment, and evidence-supported protein annotation characterized temporal and host-associated transcriptional patterns. Likelihood ratio tests identified 7,852 time-responsive genes in barley and 5,464 in wheat. Relative to 0 HAI, 2,858 to 3,868 genes were upregulated in barley and 1,631 to 3,921 in wheat, whereas downregulated genes were uncommon. Shared upregulated genes increased from 1,410 at 24 HAI to 3,192 at 96 HAI. Upregulated genes in both hosts were enriched for protein synthesis, energy metabolism, intracellular transport, and protein homeostasis. Curated DEG categories comprised candidates representing cell wall-degrading enzymes, effectors, biosynthetic gene cluster core genes, transcription factors, transporters, signaling proteins, and stress/detoxification proteins. Many categories were represented earlier or more broadly in barley but increased later in wheat, with several approaching or exceeding barley by 96 HAI. These findings reveal a shared core transcriptional program with host-associated temporal differences and provide a basis for further prioritization and functional validation of candidate genes involved in F. poae colonization and FHB development.

PMID:42799990 | DOI:10.1094/PHYTO-07-26-0235-R

Theor Appl Genet. 2026 Sep 27;139(10):282. doi: 10.1007/s00122-026-05381-9.

ABSTRACT

Crockett and PI 398469 carry distinct resistance alleles at the Rdm3 locus for soybean southern stem canker, supported by progeny analysis, sequence variation, candidate gene expression profiling, and allele transmission patterns. Genetic resistance to southern stem canker (SSC) in soybean is predominantly conditioned by the Rdm3 locus on chromosome (Chr) 14. Resistance at this locus has been identified in ‘Crockett’ and PI 398469; however, the allelic relationship between these lines remains unresolved. This study aimed to determine whether SSC resistance in Crockett and PI 398469 is governed by the same or distinct alleles at the Rdm3 locus. Progeny analysis of a Crockett × PI 398469 recombinant inbred line (RIL) population identified recombinant lines with weaker resistance and broader phenotypic variation than either parent, indicating that recombination at the Rdm3 locus disrupted favorable allele combinations and generated unexpected SSC resistance phenotypes. Consistent with this, sequence analysis of two priority candidate genes, Glyma.14G023500 and Glyma.14G022600, revealed variation associated with resistance between Crockett and PI 398469, as well as among resistant and susceptible RILs. Expression profiling of these candidate genes further demonstrated genotype-dependent temporal patterns, suggesting distinct regulatory mechanisms underlying resistance conferred by Rdm3 alleles from Crockett and PI 398469. In addition, the resistance alleles differed in their transmission behavior, with segregation distortion and underrepresentation of the Crockett allele observed across breeding populations and germplasm pools. Pedigree analysis further indicated an atypical origin of the Crockett Rdm3 allele. These results demonstrate that Crockett and PI 398469 carry functionally distinct resistance alleles at Rdm3, confirming allelic variation at a major SSC resistance locus and providing insight into the effective deployment of Rdm3 resistance in soybean breeding.

PMID:42801351 | DOI:10.1007/s00122-026-05381-9

Plant Dis. 2026 Sep 22. doi: 10.1094/PDIS-03-26-0441-RE. Online ahead of print.

ABSTRACT

Native plant restoration efforts in California are continuously challenged by Phytophthora-induced diseases, particularly through nursery introductions, resulting in significant losses and distribution of pathogens into restoration areas. Effective diagnostic strategies can help manage Phytophthora, yet determining the most suitable method, considering specificity, sampling time, resource availability, and expertise, remains uncertain. This study compares the effectiveness of five diagnostic methods: irrigation leachate baiting, ImmunoStrip® for Phytophthora, culture-based isolations, recombinase polymerase amplification (RPA, targeting genus-specific trnM-trnP-trnM locus), and quantitative polymerase chain reaction (qPCR, targeting genus-specific atp9-nad9 locus) on artificially inoculated and on naturally infested ornamental plants. For artificially inoculated plant testing, two native California ornamentals, Frangula californica and Heteromeles arbutifolia, were inoculated with three Phytophthora species: P. cinnamomi, P. cactorum, and P. cryptogea, and sampled three times, every six weeks post-inoculation. The sampled plants, along with the non-inoculated controls, were subjected to the five detection methods for Phytophthora detection. Among the detection assays, RPA, qPCR, and irrigation leachate baiting had the highest Phytophthora detection rates, regardless of the host, sampling time, or pathogen species (P < 0.01). For naturally infested plants, molecular assays consistently detected Phytophthora from three horticultural and two native nurseries (one accredited through Accreditation to Improve Restoration (AIR) program and other in process), with a subset of samples independently validated by another laboratory. The AIR-certified nursery showed no Phytophthora and the lowest detection probability across methods. These results indicate that implementing strategic detection approaches, combined with best management practices, can improve detection and prevent Phytophthora spread to wildlands.

PMID:42771457 | DOI:10.1094/PDIS-03-26-0441-RE

Ecology. 2026 Sep;107(9):e70525. doi: 10.1002/ecy.70525.

ABSTRACT

The distributions of rare species are often estimated from presence-absence data, but undetected occurrences (imperfect detection) can lead to consequential underestimates of occupancy. Despite its standard use in animal ecology, detection probability (p) is rarely incorporated into plant occupancy estimates. Plants with cryptic life stages or traits (e.g., seed banks, dormancy) may be especially prone to periods of unobservability, resulting in imperfect detection even when a species is present. We tested the hypothesis that cryptic traits lower detection by reviewing published estimates of p in plant systems. While taxa with cryptic traits, particularly annual plants with seed banks and deciduous geophytes, exhibited lower p, there was wide variation across genera and publications. We then conducted a case study of the rare, annual, aquatic plant, Gratiola amphiantha (snorkelwort), endemic to ephemerally rain-filled granite rock outcrop pools, to estimate occupancy (Ψ), p, and their environmental drivers. We found that Ψ increased with deeper soils and larger pool areas. Snorkelwort exhibited a high but imperfect p (mean p = 0.87) that varied with competing vegetation cover and census date. Modeling Ψ across varying levels of survey effort showed that ignoring imperfect detection can underestimate total occupancy estimates by up to 43%; however, our empirical p estimates indicate a minimum of just two surveys can reach 95% detection for snorkelwort. Our findings demonstrate that imperfect detection is an important and underappreciated limitation in plant occupancy studies, even for species with high detection probability. For rare plants, explicitly incorporating taxon-specific p estimates and marginally increasing survey effort can substantially improve the accuracy of occupancy models.

PMID:42775469 | DOI:10.1002/ecy.70525