复制数变异 (CNVs) 和 karyotyping分析在男性与亚精子和小精子
Xing Xin1, Peng Xu2, Nan Wang2
1Department of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Road, Wuhan, 430030, Hubei, P.R. China.
BMC medical genomics
|September 8, 2023
概括
遗传因素显著影响男性不孕. 这项研究在阿佐精子和寡精子患者中发现了常见的染色体异常和拷贝数变异 (CNV),揭示了精子生成的潜在候选基因,并提供了新的研究目标.
科学领域:
- 生殖遗传学 生殖遗传学
- 人类遗传学 人类遗传学
- 基因组医学是一种基因组医学.
背景情况:
- 遗传因素在男性不孕症条件中至关重要,例如阿佐精子和寡精子.
- 识别染色体异常和拷贝数变异 (CNVs) 对于理解这些情况至关重要.
研究的目的:
- 在患有亚精子和小精子症的患者中,使用心型定型和CNVs识别异常染色体.
- 为了阐明与这些遗传异常相关的基因.
主要方法:
- 招募了1157名被诊断患有亚精子症或小精子症的患者.
- 在769名患者身上进行了下一代测序 (NGS) 用于复制数变异 (CNV) 分析.
- 对674名患者进行了例行G频段胆型定型.
主要成果:
- 在33%和48.9%的阿佐精子和小精子患者中分别发现了异常的胆核类型和CNV.
- 47,XXY型是最常见的遗传异常 (44.18%的异常型,26.33%的CNV).
- 在受影响的患者中发现了高频率的CNV位点,包括Xp22.31和2p24.3.
结论:
- 性染色体和自体CNV位点 (例如Xp22.31,2p24.3) 和相关基因 (例如VCX,NACAP9) 是精子生成的潜在候选基因.
- 识别出常见的异常心型,CNV位点和关键基因,作为未来对男性不孕症研究的新目标.
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