Department of Medical Genetics, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey.
Department of Molecular Medicine, Graduate Institute, Ondokuz Mayis University, Samsun, Turkey.
J Assist Reprod Genet. 2022 Dec;39(12):2799-2810. doi: 10.1007/s10815-022-02632-8. Epub 2022 Oct 17.
Sex chromosome abnormalities are associated with male infertility. The aim of this study was to characterize the clinical, cytogenetic, and molecular findings of 12 infertile men with isodicentric Y-chromosome [idic(Y)] abnormalities diagnosed over a period of 13 years.
Chromosomal analyses of peripheral blood samples were done using standard procedures. Fluorescence in situ hybridization (FISH) analysis was performed on metaphase spreads of the patients. Multiplex polymerase chain reaction (PCR) using several sequence-tagged site (STS) primer sets within the long arm of Y-chromosome was used to detect AZF deletions.The breakpoints and copy number variations (CNV) were identified by array comparative genomic hybridization analysis (aCGH) analysis.The short-stature homeobox (SHOX) gene deletions were verified using multiplex ligation-dependent probe amplification (MLPA) analysis.
Twelve infertile men were diagnosed cytogenetically with idic(Y). The karyotypes of two of the patients were non-mosaic, and the remaining karyotypes showed various degrees of mosaicism. SHOX gene deletion was found in two of the four patients with short stature, and the remaining two patients had shown a 45,X dominant cell line (33.3%). The most common breakpoints for idic(Yq) and idic(Yp) were found to be in Yq11.222 and Yp11.32, respectively. Semen analysis of ten patients (83.3%) demonstrated azoospermia, and the remaining two patients (16.7%) showed severe oligoasthenoteratozoospermia (OAT). In total, 33% (4/12) of idic(Y) patients with or without microsurgical testicular sperm extraction (microTESE) had sperm retrieval.
Twelve patients with idic(Y) and different breakpoints of Y-chromosome were characterized using multiple detection strategies. Sperm retrieval outcomes of patients either with idic(Yp) or idic(Yq) showed the possibility to find sperm by microTESE.
性染色体异常与男性不育有关。本研究的目的是描述 12 名患有等臂 Y 染色体[idic(Y)]异常的不育男性患者的临床、细胞遗传学和分子特征,这些患者的诊断时间跨度为 13 年。
采用标准程序对外周血样本进行染色体分析。对患者的中期分裂进行荧光原位杂交(FISH)分析。使用 Y 染色体长臂内的多个序列标记位点(STS)引物组进行多重聚合酶链反应(PCR),以检测 AZF 缺失。通过比较基因组杂交分析(aCGH)分析鉴定断点和拷贝数变异(CNV)。使用多重连接依赖性探针扩增(MLPA)分析验证短体同源盒(SHOX)基因缺失。
12 名不育男性被诊断为idic(Y)核型异常。两名患者的核型为非嵌合体,其余核型显示不同程度的嵌合体。在四名身材矮小的患者中发现了 SHOX 基因缺失,其余两名患者表现出 45,X 优势细胞系(33.3%)。idic(Yq)和idic(Yp)的最常见断点分别位于 Yq11.222 和 Yp11.32。10 名患者(83.3%)的精液分析显示无精子症,其余 2 名患者(16.7%)表现为严重少弱畸形精子症(OAT)。总共 33%(4/12)的有或没有微创睾丸精子提取(microTESE)的 idic(Y)患者获得了精子提取。
使用多种检测策略对具有不同 Y 染色体断点的 12 名 idic(Y)患者进行了特征描述。通过 microTESE,idic(Yp)或 idic(Yq)患者的精子提取结果显示出找到精子的可能性。