FB2025_01 , released February 20, 2025
Reference Report
Open Close
Reference
Citation
Wormser, O., Levy, Y., Bakhrat, A., Bonaccorsi, S., Graziadio, L., Gatti, M., AbuMadighem, A., McKenney, R.J., Okada, K., El Riati, S., Har-Vardi, I., Huleihel, M., Levitas, E., Birk, O.S., Abdu, U. (2021). Absence of SCAPER causes male infertility in humans and Drosophila by modulating microtubule dynamics during meiosis.  J. med. Genet. 58(4): 254--263.
FlyBase ID
FBrf0248471
Publication Type
Research paper
Abstract
Mutation in S-phase cyclin A-associated protein rin the endoplasmic reticulum (SCAPER) have been found across ethnicities and have been shown to cause variable penetrance of an array of pathological traits, including intellectual disability, retinitis pigmentosa and ciliopathies. Human clinical phenotyping, surgical testicular sperm extraction and testicular tissue staining. Generation and analysis of short spindle 3 (ssp3) (SCAPER orthologue) Drosophila CAS9-knockout lines. In vitro microtubule (MT) binding assayed by total internal reflection fluorescence microscopy. We show that patients homozygous for a SCAPER mutation lack SCAPER expression in spermatogonia (SPG) and are azoospermic due to early defects in spermatogenesis, leading to the complete absence of meiotic cells. Interestingly, Drosophila null mutants for the ubiquitously expressed ssp3 gene are viable and female fertile but male sterile. We further show that male sterility in ssp3 null mutants is due to failure in both chromosome segregation and cytokinesis. In cells undergoing male meiosis, the MTs emanating from the centrosomes do not appear to interact properly with the chromosomes, which remain dispersed within dividing spermatocytes (SPCs). In addition, mutant SPCs are unable to assemble a normal central spindle and undergo cytokinesis. Consistent with these results, an in vitro assay demonstrated that both SCAPER and Ssp3 directly bind MTs. Our results show that SCAPER null mutations block the entry into meiosis of SPG, causing azoospermia. Null mutations in ssp3 specifically disrupt MT dynamics during male meiosis, leading to sterility. Moreover, both SCAPER and Ssp3 bind MTs in vitro. These results raise the intriguing possibility of a common feature between human and Drosophila meiosis.
PubMed ID
PubMed Central ID
PMC10405349 (PMC) (EuropePMC)
Related Publication(s)
Personal communication to FlyBase

ssp3 deletion location information.
Abdu, 2021.8.19, ssp3 deletion location information. [FBrf0250299]

Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Compendium
    Abbreviation
    J. med. Genet.
    Title
    Journal of Medical Genetics
    Publication Year
    1964-
    ISBN/ISSN
    0022-2593
    Data From Reference
    Aberrations (1)
    Alleles (9)
    Genes (2)
    Human Disease Models (1)
    Insertions (5)
    Experimental Tools (2)
    Transgenic Constructs (5)