Novel homozygous variations in PLCZ1 lead to poor or failed fertilization characterized by abnormal localization patterns of PLCζ in sperm

Clin Genet. 2020 Feb;97(2):347-351. doi: 10.1111/cge.13636. Epub 2019 Sep 8.

Abstract

Total fertilization failure (TFF), which is the failure of fertilization in all oocytes, occurs in 1%-3% of intracytoplasmic sperm injection (ICSI) cycles. However, the sperm-related factors that cause fertilization failure in humans are still largely unknown. Here, we identified three novel homozygous variations in the PLCZ1 gene in a recessive inheritance pattern in three consanguineous families, which all located in a key catalytic domain, and predicted to modify its secondary structure and thus impair its hydrolytic activity. Moreover, immunofluorescent staining revealed that PLCζ in mutant sperm exhibited abnormal localization patterns. ICSI-AOA resulted in an increased rate of normal fertilization compared with previous ICSI cycles (75.0% vs 2.2%, P < .001). In summary, we identified three novel homozygous variations in PLCZ1 that led to poor or failed fertilization that could be overcame by ICSI-AOA.

Keywords: Phophospholipase C zeta; assisted oocyte activation; fertilization failure; variation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Consanguinity
  • Female
  • Fertilization in Vitro*
  • Homozygote
  • Humans
  • Male
  • Oocytes / metabolism
  • Phosphoinositide Phospholipase C / genetics*
  • Phosphoinositide Phospholipase C / ultrastructure
  • Protein Structure, Secondary
  • Sperm Injections, Intracytoplasmic / methods
  • Spermatozoa / metabolism
  • Spermatozoa / pathology*

Substances

  • PLCZ1 protein, human
  • Phosphoinositide Phospholipase C