FB2025_01 , released February 20, 2025
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Citation
Castillejo-López, C., Cai, X., Fahmy, K., Baumgartner, S. (2018). Drosophila exoribonuclease nibbler is a tumor suppressor, acts within the RNA(i) machinery and is not enriched in the nuage during early oogenesis.  Hereditas 155(): 12.
FlyBase ID
FBrf0236844
Publication Type
Research paper
Abstract
micro RNAs (miRNAs) are important regulators of many biological pathways. A plethora of steps are required to form, from a precursor, the mature miRNA that eventually acts on its target RNA to repress its expression or to inhibit translation. Recently, Drosophila nibbler (nbr) has been shown to be an important player in the maturation process of miRNA and piRNA. Nbr is an exoribonuclease which helps to shape the 3' end of miRNAs by trimming the 3' overhang to a final length. In contrast to previous reports on the localization of Nbr, we report that 1) Nbr is expressed only during a short time of oogenesis and appears ubiquitously localized within oocytes, and that 2) Nbr was is not enriched in the nuage where it was shown to be involved in piwi-mediated mechanisms. To date, there is little information available on the function of nbr for cellular and developmental processes. Due to the fact that nbr mutants are viable with minor deleterious effects, we used the GAL4/UAS over-expression system to define novel functions of nbr. We disclose hitherto unknown functions of nbr 1) as a tumor suppressor and 2) as a suppressor of RNA(i). Finally, we confirm that nbr is a suppressor of transposon activity. Our data suggest that nbr exerts much more widespread functions than previously reported from trimming 3' ends of miRNAs only.
PubMed ID
PubMed Central ID
PMC5622571 (PMC) (EuropePMC)
Associated Information
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Hereditas
    Title
    Hereditas
    Publication Year
    1920-
    ISBN/ISSN
    0018-0661
    Data From Reference
    Alleles (10)
    Genes (3)
    Cell Lines (1)
    Natural transposons (1)
    Insertions (2)
    Experimental Tools (2)
    Transgenic Constructs (8)