FB2024_03 , released June 25, 2024
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Citation
McGurk, L., Pathirana, S., Rothwell, K., Trimbuch, T., Colombini, P., Yu, F., Chia, W., Bownes, M. (2008). The RGS gene loco is essential for male reproductive system differentiation in Drosophila melanogaster.  BMC Dev. Biol. 8(): 37.
FlyBase ID
FBrf0205442
Publication Type
Research paper
Abstract
The loco gene encodes several different isoforms of a regulator of G-protein signalling. These different isoforms of LOCO are part of a pathway enabling cells to respond to external signals. LOCO is known to be required at various developmental stages including neuroblast division, glial cell formation and oogenesis. Less is known about LOCO and its involvement in male development therefore to gain further insight into the role of LOCO in development we carried out a genetic screen and analysed males with reduced fertility.We identified a number of lethal loco mutants and four semi-lethal lines, which generate males with reduced fertility. We have identified a fifth loco transcript and show that it is differentially expressed in developing pupae. We have characterised the expression pattern of all loco transcripts during pupal development in the adult testes, both in wild type and loco mutant strains. In addition we also show that there are various G-protein alpha subunits expressed in the testis all of which may be potential binding partners of LOCO.We propose that the male sterility in the new loco mutants result from a failure of accurate morphogenesis of the adult reproductive system during metamorphosis, we propose that this is due to a loss of expression of loco c3. Thus, we conclude that specific isoforms of loco are required for the differentiation of the male gonad and genital disc.
PubMed ID
PubMed Central ID
PMC2324087 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    BMC Dev. Biol.
    Title
    BMC Developmental Biology
    Publication Year
    2002
    ISBN/ISSN
    1471-213X
    Data From Reference
    Aberrations (2)
    Alleles (9)
    Genes (5)
    Insertions (4)
    Transgenic Constructs (2)
    Transcripts (1)