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  • Wiley  (2)
  • 2020-2024  (2)
  • 1
    In: Journal of Eukaryotic Microbiology, Wiley
    Kurzfassung: Ancyromonads are small biflagellated protists with a bean‐shaped morphology. They are cosmopolitan in marine, freshwater, and soil environments, where they attach to surfaces while feeding on bacteria. These poorly known grazers stand out by their uncertain phylogenetic position in the tree of eukaryotes, forming a deep‐branching “orphan” lineage that is considered key to a better understanding of the early evolution of eukaryotes. Despite their ecological and evolutionary interest, only limited knowledge exists about their true diversity. Here, we aimed to characterize ancyromonads better by integrating environmental surveys with behavioral observation and description of cell morphology, for which sample isolation and culturing are indispensable. We studied 18 ancyromonad strains, including 14 new isolates and seven new species. We described three new and genetically divergent genera: Caraotamonas , Nyramonas , and Olneymonas , together encompassing four species. The remaining three new species belong to the already‐known genera Fabomonas and Ancyromonas . We also raised Striomonas , formerly a subgenus of Nutomonas , to full genus status, on morphological and phylogenetic grounds. We studied the morphology of diverse ancyromonads under light and electron microscopy and carried out molecular phylogenetic analyses, also including 18S rRNA gene sequences from several environmental surveys. Based on these analyses, we have updated the taxonomy of Ancyromonadida.
    Materialart: Online-Ressource
    ISSN: 1066-5234 , 1550-7408
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2023
    ZDB Id: 2126326-7
    SSG: 12
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    In: Cancer Science, Wiley, Vol. 112, No. 8 ( 2021-08), p. 3375-3387
    Kurzfassung: Succinate dehydrogenase (SDH)‐deficient renal cell carcinoma (RCC) is mainly associated with a mutation in the SDHB gene and sometimes with mutations in the SDHC or SDHD genes. However, only three cases of succinate dehydrogenase A (SDHA)‐deficient RCC have been reported, and the relation between SDHA mutations and RCC has not been clarified. This study assessed the role of SDHA gene mutations in human RCC. We investigated SDHA/B/C/D gene mutations in 129 human RCCs. Targeted next‐generation sequencing and direct Sanger sequencing revealed single nucleotide variants (SNVs) of the SDHA gene with amino acid sequence variations in 11/129 tumors, while no SDHB/C/D gene mutations were found. Tumor cells with SNVs of the SDHA gene were characterized by eosinophilic cytoplasm and various patterns of proliferation. Immunohistochemistry examination found that the 11 tumors with SNVs of the SDHA gene showed significant reduction of SDHA protein and SDHB protein expression compared to the 19 tumors without SDHA or SDHB mutations (both P   〈  .0001). Western blotting showed a greater decrease in the expression of SDHA and SDHB proteins in the 11 tumors with SNVs of the SDHA gene than in the 19 tumors without (both P   〈  .0001). There was a positive correlation between SDHA and SDHB protein levels ( P   〈  .0001). On immunohistochemistry and Western blotting, the 11 tumors with SNVs of the SDHA gene had higher protein expression for nuclear factor E2‐related factor 2 (Nrf2) compared to the 19 tumors without the mutation ( P   〈  .01). These observations suggest that SDHA gene mutations might be associated with a subset of RCC.
    Materialart: Online-Ressource
    ISSN: 1347-9032 , 1349-7006
    URL: Issue
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2021
    ZDB Id: 2115647-5
    ZDB Id: 2111204-6
    Standort Signatur Einschränkungen Verfügbarkeit
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