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1.
Comput Struct Biotechnol J ; 21: 401-417, 2023.
Article in English | MEDLINE | ID: mdl-36618980

ABSTRACT

Modification of tRNA is an integral part of the epitranscriptome with a particularly pronounced potential to generate diversity in RNA expression. Eukaryotic tRNA contains modifications in up to 20% of their nucleotides, but not all sites are always fully modified. Combinations and permutations of partially modified sites in tRNAs can generate a plethora of tRNA isoforms, termed modivariants. Here, we investigate the stoichiometry of incompletely modified sites in tRNAs from human cell lines for their information content. Using a panel of RNA modification mapping methods, we assess the stoichiometry of sites that contain the modifications 5-methylcytidine (m5C), 2'-O-ribose methylation (Nm), 3-methylcytidine (m3C), 7-methylguanosine (m7G), and Dihydrouridine (D). We discovered that up to 75% of sites can be incompletely modified and that the differential modification status of a cellular tRNA population holds information that allows to discriminate e.g. different cell lines. As a further aspect, we investigated potential causal connectivity between tRNA modification and its processing into tRNA fragments (tiRNAs and tRFs). Upon exposure of cultured living cells to cell-penetrating angiogenin, the modification patterns of the corresponding RNA populations was changed. Importantly, we also found that tsRNAs were significantly less modified than their parent tRNAs at numerous sites, suggesting that tsRNAs might derive chiefly from hypomodified tRNAs.

2.
Nat Genet ; 50(3): 375-380, 2018 03.
Article in English | MEDLINE | ID: mdl-29434356

ABSTRACT

Host resistance and fungicide treatments are cornerstones of plant-disease control. Here, we show that these treatments allow sex and modulate parenthood in the fungal wheat pathogen Zymoseptoria tritici. We demonstrate that the Z. tritici-wheat interaction complies with the gene-for-gene model by identifying the effector AvrStb6, which is recognized by the wheat resistance protein Stb6. Recognition triggers host resistance, thus implying removal of avirulent strains from pathogen populations. However, Z. tritici crosses on wheat show that sex occurs even with an avirulent parent, and avirulence alleles are thereby retained in subsequent populations. Crossing fungicide-sensitive and fungicide-resistant isolates under fungicide pressure results in a rapid increase in resistance-allele frequency. Isolates under selection always act as male donors, and thus disease control modulates parenthood. Modeling these observations for agricultural and natural environments reveals extended durability of host resistance and rapid emergence of fungicide resistance. Therefore, fungal sex has major implications for disease control.


Subject(s)
Ascomycota/pathogenicity , Drug Resistance, Fungal/genetics , Pollination , Protein Kinases/genetics , Stress, Physiological , Strobilurins/pharmacology , Triticum/genetics , Agriculture , Ascomycota/drug effects , Chromosome Mapping , Chromosomes, Plant , Epistasis, Genetic , Fungicides, Industrial/pharmacology , Host-Pathogen Interactions/drug effects , Host-Pathogen Interactions/genetics , Plant Diseases/genetics , Plant Diseases/microbiology , Plant Diseases/prevention & control , Pollination/drug effects , Pollination/genetics , Protein Kinases/physiology , Stress, Physiological/drug effects , Stress, Physiological/genetics , Triticum/physiology
3.
Phytopathology ; 106(10): 1206-1212, 2016 10.
Article in English | MEDLINE | ID: mdl-27050568

ABSTRACT

Microbial pathogens cause devastating diseases on economically and ecologically important plant species, threatening global food security, and causing billions of dollars of losses annually. During the infection process, pathogens secrete so-called effectors that support host colonization, often by deregulating host immune responses. Over the last decades, much of the research on molecular plant-microbe interactions has focused on the identification and functional characterization of such effectors. The increasing availability of sequenced plant pathogen genomes has enabled genomics-based discovery of effector candidates. Nevertheless, identification of full plant pathogen effector repertoires is often hampered by erroneous gene annotation and the localization effector genes in genomic regions that are notoriously difficult to assemble. Here, we argue that recent advances in genome sequencing technologies, genome assembly, gene annotation, as well as effector identification methods hold promise to disclose complete and correct effector repertoires. This allows to exploit complete effector repertoires, and knowledge of their diversity within pathogen populations, to develop durable and sustainable resistance breeding strategies, disease control, and management of plant pathogens.


Subject(s)
Genome, Microbial/genetics , Genomics , Plant Diseases/prevention & control , Breeding , Molecular Sequence Annotation , Plant Diseases/microbiology
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