Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal

Analyses in our diagnostic DNA laboratory include genes involved in autosomal recessive (AR) lysosomal storage disorders such as glycogenosis type II (Pompe disease) and mucopolysaccharidosis type I (MPSI, Hurler disease). We encountered 4 cases with apparent homozygosity for a disease-causing sequence variant that could be traced to one parent only. In addition, in a young child with cardiomyopathy, in the absence of other symptoms, a diagnosis of Pompe disease was considered. Remarkably, he presented with different enzymatic and genotypic features between leukocytes and skin fibroblasts. All cases were examined with microsatellite markers and SNP genotyping arrays. We identified one case of total uniparental disomy (UPD) of chromosome 17 leading to Pompe disease and three cases of segmental uniparental isodisomy (UPiD) causing Hurler-(4p) or Pompe disease (17q). One Pompe patient with unusual combinations of features was shown to have a mosaic segmental UPiD of chromosome 17q. The chromosome 17 UPD cases amount to 11% of our diagnostic cohort of homozygous Pompe patients (plus one case of pseudoheterozygosity) where segregation analysis was possible. We conclude that inclusion of parental DNA is mandatory for reliable DNA diagnostics. Mild or unusual phenotypes of AR diseases should alert physicians to the possibility of mosaic segmental UPiD. SNP genotyping arrays are used in diagnostic workup of patients with developmental delay. Our results show that even small Regions of Homozygosity that include telomeric areas are worth reporting, regardless of the imprinting status of the chromosome, as they might indicate segmental UPiD

C60 exposure induced tissue damage and gene expression alterations in the earthworm Lumbricus rubellus

Effects of C60 exposure (0, 15 or 154 mg/kg soil) on the earthworm Lumbricus rubellus were assessed at the tissue and molecular level, in two experiments. In the first experiment, earthworms were exposed for four weeks, and in the second lifelong. In both experiments, gene expression of heat shock protein 70 (HSP70) decreased. For catalase and glutathione-S-transferase (GST), no significant trends in gene expression or enzyme activity were observed. Gene expression of coelomic cytolytic factor-1 (CCF-1) did not alter in earthworms exposed for four weeks, but was significantly down-regulated in the lifelong exposure. Histology of earthworms exposed to C60 in both experiments showed a damaged cuticle, with underlying pathologies of epidermis and muscles, as well as effects on the gut barrier. However, tissue repair was also observed in these earthworms. Overall, these data show that sub-lethal C60 exposure to earthworms via the soil affects gene expression and causes tissue pathologies. Keywords: Nanoparticles, soil organisms, histology, gene expression, enzyme activit

C60 exposure induced tissue damage and gene expression alterations in the earthworm Lumbricus rubellus

Effects of C60 exposure (0, 15 or 154 mg/kg soil) on the earthworm Lumbricus rubellus were assessed at the tissue and molecular level, in two experiments. In the first experiment, earthworms were exposed for four weeks, and in the second lifelong. In both experiments, gene expression of heat shock protein 70 (HSP70) decreased. For catalase and glutathione-S-transferase (GST), no significant trends in gene expression or enzyme activity were observed. Gene expression of coelomic cytolytic factor-1 (CCF-1) did not alter in earthworms exposed for four weeks, but was significantly down-regulated in the lifelong exposure. Histology of earthworms exposed to C60 in both experiments showed a damaged cuticle, with underlying pathologies of epidermis and muscles, as well as effects on the gut barrier. However, tissue repair was also observed in these earthworms. Overall, these data show that sub-lethal C60 exposure to earthworms via the soil affects gene expression and causes tissue pathologies. Keywords: Nanoparticles, soil organisms, histology, gene expression, enzyme activit