不耐受基因中的有害变异揭示了自我限制的延迟青春期的新候选人
Raíssa C Rezende1, Wen He2, Lena R Kaisinger3
1Unidade de Endocrinologia Genetica (LIM 25), Hospital das Clínicas da Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, SP 0124690, Brazil.
这项研究确定了自我限制性延迟青春期 (SLDP) 的新型候选基因,这是一个常见的疾病. 结果表明SLDP的单基因和多基因原因,突出INHBBBB.
科学领域:
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
- 儿科 儿科 儿科
背景情况:
- 自限性延迟青春期 (SLDP) 是延迟青春期的最常见原因.
- 虽然SLDP具有很高的遗传性,但只有很少的因果基因被确定.
- 识别遗传因素对于理解SLDP病理生理学至关重要.
研究的目的:
- 为了确定与自我限制延迟青春期 (SLDP) 相关的潜在候选基因.
- 探索SLDP的遗传基础,包括单基因和多基因机制.
主要方法:
- 在71名患有SLDP的儿童中进行整体外体测序.
- 稀有编码变体的生物信息优先级.
- 负载测试比较病例和对照 (gnomAD v2.0). 这是一个负载测试.
- 用英国生物银行数据进行基因表型关联分析.
主要成果:
- 19个候选基因被确定具有高或中等影响的变体.
- 在8个候选基因 (GPS1,INHBB,SP3,NAMPT,ARID3B,NASP,FNBP1,PRDM2) 中显著丰富变异.
- INHHB与初潮延迟有关;其他已知的致病性/可能致病性变体被确定.
结论:
- SLDP涉及单基因和多基因遗传机制.
- 新型候选基因有助于SLDP的遗传基础.
- 基因INHBB与青春期的时间相关,这表明它在SLDP中发挥了作用.
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