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Identification of Copy Number Variants in a Cohort of Women with Premature Ovarian Insufficiency

机译:卵巢早衰妇女队列中拷贝数变异的鉴定

摘要

Premature ovarian failure (POF), or premature ovarian insufficiency (POI), is characterized by the absence or early cessation of menstruation before the age of 40. Clinically this can be seen as primary amenorrhea, the complete absence of menstruation, or secondary amenorrhea, the development of amenorrhea due to cessation of ovarian function. POI affects approximately 1% of women under the age of 40 years and 0.1% of women under the age of 30. Most cases of POI are idiopathic, as only 10% have a known cause. We utilized SNP array technology to identify novel copy number variations (CNV's) in 89 women with POI. Illumina's (San Diego, CA, USA) HumanCNV370-Duo DNA Analysis BeadChip and Human660W-Quad v1 DNA Analysis BeadChip were used to identify microdeletions and microduplications on autosomal chromosomes. A total of 198 autosomal CNV's were identified ranging from 0.1 Mb to 3.4 Mb. The Database of Genomic Variants (DGV) was used as a control population. We identified seven novel microdeletions in our POI cohort, six of which contained gene-coding regions: 8q24.13, 10p15-p14, 10q23.31, 10q26.3, 15q25.2, and 18q21.32. Two of the novel microdeletions contained genes known to cause ovarian failure in knockout mice models, SYCE1 and CPEB1. Seventeen novel microduplications were also detected, with the majority of CNV's detected being on autosomal chromosomes rather than the X chromosome. This pilot study demonstrates an association between specific CNV's and POI and highlights the importance for studies with larger samples sizes to confirm the findings and further support the hypothesis. Furthermore, array technology may be a useful addition to conventional karyotyping when evaluating women with POI. Studies on the genetic factors of POI have public health significance because they search for genomic imbalances in a disease that affects 1% of the American population. Finding the genetic causes may lead to effective treatment methods and earlier recognition of those at risk, particularly before the onset of amenorrhea.
机译:卵巢早衰(POF)或卵巢早衰(POI)的特征是在40岁之前没有月经或提早停止月经。在临床上,这可被视为原发性闭经,月经完全消失或继发性闭经,卵巢功能停止导致闭经的发展。 POI会影响大约1%的40岁以下女性和0.1%的30岁以下的女性。大多数POI病例是特发性的,因为只有10%的原因是已知的。我们利用SNP阵列技术确定了89名POI女性的新型拷贝数变异(CNV)。 Illumina(美国加利福尼亚州圣地亚哥)的HumanCNV370-Duo DNA分析BeadChip和Human660W-Quad v1 DNA分析BeadChip用于鉴定常染色体上的微缺失和微重复。共鉴定出198个常染色体CNV,范围从0.1 Mb到3.4 Mb。使用基因组变异数据库(DGV)作为对照种群。我们在POI队列中鉴定了7个新的微缺失,其中6个包含基因编码区:8q24.13、10p15-p14、10q23.31、10q26.3、15q25.2和18q21.32。两种新的微缺失包含已知在敲除小鼠模型中引起卵巢衰竭的基因,即SYCE1和CPEB1。还检测到十七种新颖的微重复,其中检测到的大部分CNV位于常染色体而不是X染色体上。这项先导研究证明了特定CNV与POI之间的关联,并强调了进行更大样本量研究以确认发现并进一步支持该假设的重要性。此外,在对女性进行POI评估时,阵列技术可能是常规核型分析的有用补充。关于POI遗传因素的研究具有公共卫生意义,因为它们寻找影响1%的美国人口的疾病的基因组失衡。寻找遗传原因可能导致有效的治疗方法,并早日识别有风险的人,尤其是在闭经发作之前。

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    Engel Natalie Joy;

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