Research demonstrates ZZ domain deletion disrupts spermatid individualization in Drosophila, indicating RNA-binding importance.
ORB2 is the Drosophila ortholog of the human CPEB2-4 family of RNA-binding proteins, which include a conserved C-terminal Zinc-binding (ZZ) domain. We have recently shown that this domain interacts with several translation co-repressors in the early embryo, and that deletion of this domain from the endogenous orb2 gene results in derepression of its target mRNAs (Low et al. 2025). Here we assess the effect of deletion of the ZZ domain on spermatogenesis. We find that ORB2ZZ protein is no longer localized to the distal tip of spermatids; that in orb2 ZZ testes, additional proteins known to play a role in spermatid individualization ORB, IMP, SOTI are mislocalized; that the SOTI-dependent Cleaved Caspase 3 gradient no longer forms; that individualization complexes are defective; and that orb2 ZZ flies are sterile and lack mature sperm.
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Low et al. (2025) studied this question.
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