AI Article Synopsis

  • Sperm fertilization depends on effective movement through the female reproductive system and a process called capacitation, which is influenced by specific signaling pathways.
  • Researchers studied an infertile patient with poor sperm motility and found harmful genetic variants affecting proteins related to sperm function.
  • The study reveals that these genetic mutations impair sperm's ability to undergo necessary chemical changes for successful fertilization and identifies a crucial protein, IQCH, essential for sperm movement and capacitation.

Article Abstract

Sperm fertilization ability mainly relies on proper sperm progression through the female genital tract and capacitation, which involves phosphorylation signaling pathways triggered by calcium and bicarbonate. We performed exome sequencing of an infertile asthenozoospermic patient and identified truncating variants in , encoding a microtubule-associated protein, and , encoding a protein of unknown function with enzymatic and signaling features. We demonstrate the deleterious impact of both variants on sperm transcripts and proteins from the patient. We show that, , patient spermatozoa could not induce the phosphorylation cascades associated with capacitation. We also provide evidence for IQCH association with calmodulin, a well-established calcium-binding protein that regulates the calmodulin kinase. Notably, we describe IQCH spatial distribution around the sperm axoneme, supporting its function within flagella. Overall, our work highlights the cumulative pathological impact of gene mutations and identifies IQCH as a key protein required for sperm motility and capacitation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382937PMC
http://dx.doi.org/10.1016/j.isci.2023.107354DOI Listing

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