Department of Genetics at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
J Hum Genet. 2019 Oct;64(10):1023-1032. doi: 10.1038/s10038-019-0642-0. Epub 2019 Jul 18.
Obstructive azoospermia (OA), defined as an obstruction in any region of the male genital tract, accounts for 40% of all azoospermia cases. Of all OA cases, ~30% are thought to have a genetic origin, however, hitherto, the underlying genetic etiology of the majority of these cases remain unknown. To address this, we took a family-based whole-exome sequencing approach to identify causal variants of OA in a multiplex family with epidydimal obstruction. A novel gain-of-function missense variant in CLDN2 (c.481G>C; p.Gly161Arg) was found to co-segregate with the phenotype, consistent with the X-linked inheritance pattern observed in the pedigree. To assess the pathogenicity of this variant, the wild and mutant protein structures were modeled and their potential for strand formation in multimeric form was assessed and compared. The results showed that dimeric and tetrameric arrangements of Claudin-2 were not only reduced, but were also significantly altered by this single residue change. We, therefore, envisage that this amino acid change likely forms a polymeric discontinuous strand, which may lead to the disruption of tight junctions among epithelial cells. This missense variant is thus likely to be responsible for the disruption of the blood-epididymis barrier, causing dislodged epithelial cells to clog the genital tract, hence causing OA. This study not only sheds light on the underlying pathobiology of OA, but also provides a basis for more efficient diagnosis in the clinical setting.
梗阻性无精子症(OA)定义为男性生殖道任何部位的梗阻,占无精子症病例的 40%。在所有 OA 病例中,约 30%被认为具有遗传起源,然而,迄今为止,这些病例的大多数潜在遗传病因仍然未知。为了解决这个问题,我们采用基于家系的全外显子组测序方法,在一个具有附睾梗阻的多灶性家系中鉴定 OA 的因果变异。发现 CLDN2 中的一个新的功能获得性错义变异(c.481G>C;p.Gly161Arg)与表型共分离,符合家系中观察到的 X 连锁遗传模式。为了评估该变异的致病性,对野生型和突变型蛋白质结构进行建模,并评估和比较其在多聚体形式下形成链的潜力。结果表明,Claudin-2 的二聚体和四聚体排列不仅减少,而且由于这单个残基的变化而显著改变。因此,我们设想该氨基酸变化可能形成聚合不连续链,这可能导致上皮细胞之间的紧密连接中断。因此,该错义变异很可能导致血附睾屏障的破坏,导致脱落的上皮细胞堵塞生殖道,从而导致 OA。这项研究不仅揭示了 OA 的潜在病理生物学机制,还为临床环境中的更有效诊断提供了依据。