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"Thaller, Denise"
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Comparative analysis of genome-scale, base-resolution DNA methylation profiles across 580 animal species
by
Schuster, Linda C
,
Bock, Christoph
,
Klughammer, Johanna
in
631/114/2114
,
631/208/177
,
631/208/212/2304
2023
Methylation of cytosines is a prototypic epigenetic modification of the DNA. It has been implicated in various regulatory mechanisms across the animal kingdom and particularly in vertebrates. We mapped DNA methylation in 580 animal species (535 vertebrates, 45 invertebrates), resulting in 2443 genome-scale DNA methylation profiles of multiple organs. Bioinformatic analysis of this large dataset quantified the association of DNA methylation with the underlying genomic DNA sequence throughout vertebrate evolution. We observed a broadly conserved link with two major transitions—once in the first vertebrates and again with the emergence of reptiles. Cross-species comparisons focusing on individual organs supported a deeply conserved association of DNA methylation with tissue type, and cross-mapping analysis of DNA methylation at gene promoters revealed evolutionary changes for orthologous genes. In summary, this study establishes a large resource of vertebrate and invertebrate DNA methylomes, it showcases the power of reference-free epigenome analysis in species for which no reference genomes are available, and it contributes an epigenetic perspective to the study of vertebrate evolution.
Journal Article
Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs
by
Weber, Corinna
,
Kleiter, Miriam
,
Jagannathan, Vidhya
in
Amino acid sequence
,
Animal euthanasia
,
Animal models
2021
We investigated a hereditary cerebellar ataxia in Belgian Shepherd dogs. Affected dogs developed uncoordinated movements and intention tremor at two weeks of age. The severity of clinical signs was highly variable. Histopathology demonstrated atrophy of the CNS, particularly in the cerebellum. Combined linkage and homozygosity mapping in a family with four affected puppies delineated a 52 Mb critical interval. The comparison of whole genome sequence data of one affected dog to 735 control genomes revealed a private homozygous structural variant in the critical interval, Chr4:66,946,539_66,963,863del17,325. This deletion includes the entire protein coding sequence of SELENOP and is predicted to result in complete absence of the encoded selenoprotein P required for selenium transport into the CNS. Genotypes at the deletion showed the expected co-segregation with the phenotype in the investigated family. Total selenium levels in the blood of homozygous mutant puppies of the investigated litter were reduced to about 30% of the value of a homozygous wildtype littermate. Genotyping >600 Belgian Shepherd dogs revealed an additional homozygous mutant dog. This dog also suffered from pronounced ataxia, but reached an age of 10 years. Selenop -/- knock-out mice were reported to develop ataxia, but their histopathological changes were less severe than in the investigated dogs. Our results demonstrate that deletion of the SELENOP gene in dogs cause a defect in selenium transport associated with CNS atrophy and cerebellar ataxia (CACA). The affected dogs represent a valuable spontaneous animal model to gain further insights into the pathophysiological consequences of CNS selenium deficiency.
Journal Article
Neoplastic mass involving the zygomatic arch in a sheep: clinical, sonographic, radiographic, pathological, and CT findings
by
Thaller, Denise
,
Hund, Alexandra
,
Gumpenberger, Michaela
in
Arthritis
,
Case reports
,
computed tomography (ct)
2018
A five-year-old intact female East Friesian sheep was presented for examination, following a noted decrease in feed intake and general apathy. A swelling was observed under the right eye. Ultrasonographic examination exposed a mass with a highly irregular texture and distinct loss of the normal bone surface echogenicity of the zygomatic and temporal processes. An ultrasound-guided fine-needle aspirate was performed which showed that the mass was a malignant spindle-cell sarcoma. The sheep was euthanased and a postmortem CT examination revealed extensive damage to the tissues surrounding the mass. Immunohistochemical staining helped to confirm the diagnosis fibrosarcoma. This case shows the value of using ultrasonography in working up such cases in general practice. The technology is available to most farm animal veterinarians and, in the authors’ opinion, should be used more extensively in practice.
Journal Article
Comparative analysis of genome-scale, base-resolution DNA methylation profiles across 580 animal species
2022
Methylation of cytosines is the prototypic epigenetic modification of the DNA. It has been implicated in various regulatory mechanisms throughout the animal kingdom and particularly in vertebrates. We mapped DNA methylation in 580 animal species (535 vertebrates, 45 invertebrates), resulting in 2443 genome-scale, base-resolution DNA methylation profiles of primary tissue samples from various organs. Reference-genome independent analysis of this comprehensive dataset quantified the association of DNA methylation with the underlying genomic DNA sequence throughout vertebrate evolution. We observed a broadly conserved link with two major transitions – once in the first vertebrates and again with the emergence of reptiles. Cross-species comparisons focusing on individual organs supported a deeply conserved association of DNA methylation with tissue type, and cross-mapping analysis of DNA methylation at gene promoters revealed evolutionary changes for orthologous genes with conserved DNA methylation patterns. In summary, this study establishes a large resource of vertebrate and invertebrate DNA methylomes, it showcases the power of reference-free epigenome analysis in species for which no reference genomes are available, and it contributes an epigenetic perspective to the study of vertebrate evolution.