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Pfeifer, M.

Publications and source records attributed to Pfeifer, M..

11 recordsLinked to original sources

Inoculation of Malus baccata 'Jackii'-derived offspring and QTL analysis reveal a polygenic inheritance pattern of apple blotch resistance

Apple blotch, caused by Diplocarpon coronariae, is an increasingly important fungal disease that leads to premature leaf fall and significant yield losses in apple orchards. Breeding resistant cultivars offers a sustainable strategy to reduce disease impact, as all commercial apple cultivars are susceptible to this pathogen. This study aimed to investigate the disease resistance of Malus baccata Jackii-derived offspring to D. coronariae through artificial inoculation and to identify loci associated with resistance. Simple interval mapping was performed using phenotypic and genotypic data from 122 individuals of an F1 population (Idared x M. baccata Jackii), together with analyses of M. baccata Jackii-derived open-pollinated populations. Our results indicate that resistance to apple blotch is a complex, polygenic trait, with four important QTLs identified on linkage groups 1, 2, 12 and 13. Disease severity was strongly affected by inoculum, phenotyping method and environmental factors. These findings have direct implications for apple breeding programmes aimed at developing apple blotch-resistant cultivars.

genetics↗

Stand age drives changes in the biodiversity and microclimate of oil palm plantations

Tree plantation age strongly dictates its environment. As they mature, the canopy closes and habitat complexity tends to increase, which in turn affects biodiversity. However, for oil palm, one of the most important and widespread tree plantations, we lack a detailed understanding of how this process affects microclimate and biodiversity. We therefore compiled environmental and biodiversity data of oil palm plantations that were repeatedly sampled over a 6 year period in Malaysian Borneo. Using these data, we made a chronosequence of the microclimate and biodiversity of oil palm plantations between the ages 5 and 18. We found that oil palm plantations increasingly buffer temperature and humidity over time, becoming cooler and less dry. Animal responses differed between taxa: spider and beetle abundance increased, ant abundance decreased, and mammal and dung-beetle abundances stayed constant. The diversity of beetles in general increased and family-level community composition changed, while dung-beetle and mammal diversity stayed constant. Some taxa are therefore likely limited by the harsh microclimate of young plantations, while increased habitat complexity and fruit and leaf production in older plantations could also drive increased abundances of other taxa. Our results reveal that oil palm plantations undergo considerable changes, even over a decade after establishment. Correspondingly, plantation age should be considered in studies into oil palm plantations impact on climate and biodiversity, and landscape level diversity could be increased by allowing multiple oil palm stand-ages to co-exist.

ecology↗

Genetic mapping, marker development, and identification of candidate genes for powdery mildew resistance in Malus baccata 'Jackii'

Powdery mildew, caused by Podosphaera leucotricha, is one of the most important fungal diseases in apple cultivation worldwide. Malus baccata Jackii, however, exhibits resistance to this pathogen, and a previous study demonstrated that this resistance co-segregates with an AFLP marker on linkage group 10. The objectives of this study were to construct genetic linkage maps, develop molecular markers, and identify candidate genes associated with this powdery mildew resistance, making use of the Malus baccata Jackii genome sequence. An F1 population derived from the cross Idared x Malus baccata Jackii was phenotyped from 2009-11 and 2023-24 and genotyped with SNPs generated from tGBS and SSRs. Genetic linkage maps of Malus baccata Jackii were constructed, and QTL mapping confirmed the presence of the powdery mildew resistance locus Plbj on linkage group 10. In addition, a minor QTL was detected on linkage group five. Closely linked SSR and KASP markers were developed, and the Plbj locus was delimited to a 3,287,286-bp region on haplotype one of the Malus baccata Jackii genome, in which resistance gene candidates were identified. This study supports the direct application of molecular markers in breeding programmes and provides an essential background for future functional studies of Plbj.

genetics↗

High-quality haplotype-resolved genome assembly and annotation of Malus baccata 'Jackii'

Malus baccata Jackii has been observed to exhibit multiple disease resistances, thus rendering it a promising source for breeding new disease-resistant apple cultivars. Here, we present the first haplotype-resolved genome assembly and annotation of this genotype, achieved by integrating PacBio HiFi sequencing, Hi-C, and mRNA sequencing data with a range of bioinformatic tools and databases. The genome assembly comprises 17 pseudochromosomes with total scaffold lengths of 654.6 Mb and 637.5 Mb for the two haplotypes, respectively. Both haplotypes have scaffold N50 values exceeding 30 Mb, with 42,441 and 46,507 predicted genes, of which 99.9% were successfully annotated. The high quality of this genome is supported by BUSCO analysis values exceeding 97.5% for both haplotypes. This comprehensive dataset is well suited for a wide range of future genomic analyses and is anticipated to benefit apple breeding, particularly in the context of enhancing disease resistance.

genomics↗

Data- and knowledge-derived functional landscape of human solute carriers

Research on the understudied solute carrier (SLC) superfamily of membrane transporters would greatly profit from a comprehensive knowledgebase, synthesizing data and knowledge on different aspects of SLC function. We consolidated multi-omics data sets with selected curated information from the public domain, such as structure prediction, substrate annotation, disease association and subcellular localization. This SLC-centric knowledge is made accessible to the scientific community via a web portal, featuring interactive dashboards and a tool for family-wide, tree-based visualization of SLC properties. Making use of the systematically collected and curated data sets, we selected eight feature-dimensions to compute an integrated functional landscape of human SLCs. This landscape represents various functional aspects, harmonizing local and global features of the underlying data sets, as demonstrated by inspecting structural folds and subcellular locations of selected transporters. Based on all available data sets and their integration, we assigned a biochemical/biological function to each SLC, making it one of the largest systematic annotations of human gene function and likely acting as a blueprint for future endeavours.

systems biology↗

Modeling flexible protein structure with AlphaFold2 and cross-linking mass spectrometry

We propose a pipeline that combines AlphaFold2 (AF2) and crosslinking mass spectrometry (XL-MS) to model the structure of proteins with multiple conformations. The pipeline consists of two main steps: ensemble generation using AF2, and conformer selection using XL-MS data. For conformer selection, we developed two scores - the monolink probability score (MP) and the crosslink probability score (XLP), both of which are based on residue depth. We benchmarked MP and XLP on a large dataset of decoy protein structures, and showed that our scores outperform previously developed scores. We then tested our methodology on three proteins having an open and closed conformation in the Protein Data Bank: Complement component 3 (C3), luciferase, and glutamine-binding periplasmic protein (QBP), first generating ensembles using AF2, which were then screened for the open and closed conformations using experimental XL-MS data. In five out of six cases, the most accurate model within the AF2 ensembles - or a conformation within 1 [A] of this model - was identified using crosslinks, as assessed through the XLP score. In the remaining case, only the monolinks (assessed through the MP score) successfully identified the open conformation of QBP. This serves as a compelling proof-of-concept for the effectiveness of monolinks. In contrast, the AF2 assessment score (pTM) was only able to identify the most accurate conformation in two out of six cases. Our results highlight the complementarity of AF2 with experimental methods like XL-MS, with the MP and XLP scores providing reliable metrics to assess the quality of the predicted models.

biochemistry↗

Engineering of a biosensor for intracellular aspartate

Aspartate is a limiting metabolite in proliferating cells with its production closely linked to glutamine and mitochondrial metabolism. To date, measuring aspartate concentrations in live cells was deemed impossible. We present iAspSnFR, a genetically-encoded biosensor for intracellular aspartate, engineered by displaying and screening biosensor libraries in HEK293 cells. In live cells, iAspSnFR exhibits a dynamic range of 130% fluorescence change and detects reduced aspartate levels upon glutamine deprivation or glutaminase inhibition. Furthermore, iAspSnFR tracks aspartate uptake by excitatory amino acid transporters, or of asparagine after co-expression of an asparaginase. Importantly, iAspSnFR reports aspartate depletions upon electron transport chain inhibition, and therefore it can serve as a proxy for mitochondrial respiration. Consequently, iAspSnFR can dissect the major cellular pathways of aspartate production, offering immediate applications, particularly in cancer biology, such as screening small molecules targeting aspartate and glutamine metabolism.

cell biology↗

IgG4 serum levels are not elevated in cases of Post-COVID syndrome

Recently, unexpectedly high virus-specific IgG4 levels were reported after more than two mRNA vaccinations. Class switch towards IgG4 occurs after long-term antigen exposure, downregulates immune responses and is associated with several autoimmune diseases. Here, we examined differences in antigen-specific IgG subtypes in serum samples from 64 Post-COVID patients and an equally sized cohort of convalescent controls. In both cohorts, the relative amounts of spike protein-specific IgG subtypes were comparable. IgG1 was the most frequent, followed by IgG3, IgG2, and IgG4. A difference between cohorts was observed only for IgG2, which was significantly lower in the Post-COVID cohort. Further analysis of the reactive IgG4 revealed a small but significant difference for the spike protein receptor-binding domain but not for the spike ectodomain. Since the total IgG4 levels are very low, we do not expect a biologically relevant role in Post-COVID syndrome. However, reduced virus-specific IgG2 levels could contribute to the persistence of SARS-CoV-2, causing chronic inflammation in the setting of Post-COVID syndrome.

immunology↗

Knowledge Graph-based Recommendation Framework Identifies Novel Drivers of Resistance in EGFR mutant Non-small Cell Lung Cancer

Resistance to EGFR inhibitors (EGFRi) presents a major obstacle in treating non-small cell lung cancer (NSCLC). One of the most exciting new ways to find potential resistance markers involves running functional genetic screens, such as CRISPR, followed by manual triage of significantly enriched genes. This triage process to identify high value hits resulting from the CRISPR screen involves significant manual curation that requires specialized knowledge and can take even experts several months to comprehensively complete. To find key drivers of resistance faster we built a hybrid recommendation system on top of a heterogeneous biomedical knowledge graph integrating preclinical, clinical, and literature evidence. Genes were ranked based on trade-offs between diverse types of evidence linking them to potential mechanisms of EGFRi resistance. This unbiased approach identified 36 resistance markers from >3,000 genes, reducing hit identification time from months to minutes. In addition to reproducing known resistance markers, our method identified novel resistance mechanisms that we prospectively validated.

cancer biology↗

Dissecting intratumor heterogeneity of nodal B cell lymphomas on the transcriptional, genetic, and drug response level

Tumor heterogeneity encompasses both the malignant cells and their microenvironment. While heterogeneity between individual patients is well-known to affect the efficacy of anti-cancer drugs, most personalized treatment approaches do not account for intratumor heterogeneity. We addressed this issue by studying the heterogeneity of lymph node-derived B cell non-Hodgkin lymphoma (B-NHL) by single cell RNA-sequencing (scRNA-seq) and transcriptome-informed flow cytometry. We identified transcriptionally distinct malignant subclones and compared their drug response and genomic profiles. Malignant subclones of the same patient responded strikingly different to anti-cancer drugs ex vivo, which recapitulated subclone-specific drug sensitivity during in vivo treatment. Tumor infiltrating T cells represented the majority of non-malignant cells, whose gene expression signatures were similar across all donors, whereas the frequencies of T cell subsets varied significantly between the donors. Our data provide new insights into the heterogeneity of B-NHL and highlight the relevance of intratumor heterogeneity for personalized cancer therapies.

cancer biology↗

Optical and physical mapping with local finishing enables megabase-scale resolution of agronomically important regions in the wheat genome

BackgroundNumerous scaffold-level sequences for wheat are now being released and, in this context, we report on a strategy for improving the overall assembly to a level comparable to that of the human genome.\n\nResultsUsing chromosome 7A of wheat as a model, sequence-finished megabase scale sections of this chromosome were established by combining a new independent assembly based on a BAC-based physical map, BAC pool paired end sequencing, chromosome arm specific mate-pair sequencing and Bionano optical mapping with the IWGSC RefSeq v1.0 sequence and its underlying raw data. The combined assembly results in 18 super-scaffolds across the chromosome. The value of finished genome regions is demonstrated for two approximately 2.5 Mb regions associated with yield and the grain quality phenotype of fructan carbohydrate grain levels. In addition, the 50 Mb centromere region analysis incorporates cytological data highlighting the importance of non-sequence data in the assembly of this complex genome region.\n\nConclusionsSufficient genome sequence information is shown to be now available for the wheat community to produce sequence-finished releases of each chromosome of the reference genome. The high-level completion identified that an array of seven fructosyl transferase genes underpins grain quality and yield attributes are affected by five f-box-only-protein-ubiquitin ligase domain and four root-specific lipid transfer domain genes. The completed sequence also includes the centromere.

genomics↗