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在胼胝体发育不全中,罕见的和新生的拷贝数变异很常见,但在小脑发育不良或多小脑回中则不然。

Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

机构信息

Department of Pediatrics, Section of Neurology, Baylor College of Medicine, Houston, Texas, United States of America.

出版信息

PLoS Genet. 2013;9(10):e1003823. doi: 10.1371/journal.pgen.1003823. Epub 2013 Oct 3.

Abstract

Agenesis of the corpus callosum (ACC), cerebellar hypoplasia (CBLH), and polymicrogyria (PMG) are severe congenital brain malformations with largely undiscovered causes. We conducted a large-scale chromosomal copy number variation (CNV) discovery effort in 255 ACC, 220 CBLH, and 147 PMG patients, and 2,349 controls. Compared to controls, significantly more ACC, but unexpectedly not CBLH or PMG patients, had rare genic CNVs over one megabase (p = 1.48×10⁻³; odds ratio [OR] = 3.19; 95% confidence interval [CI] = 1.89-5.39). Rare genic CNVs were those that impacted at least one gene in less than 1% of the combined population of patients and controls. Compared to controls, significantly more ACC but not CBLH or PMG patients had rare CNVs impacting over 20 genes (p = 0.01; OR = 2.95; 95% CI = 1.69-5.18). Independent qPCR confirmation showed that 9.4% of ACC patients had de novo CNVs. These, in comparison to inherited CNVs, preferentially overlapped de novo CNVs previously observed in patients with autism spectrum disorders (p = 3.06×10⁻⁴; OR = 7.55; 95% CI = 2.40-23.72). Interestingly, numerous reports have shown a reduced corpus callosum area in autistic patients, and diminished social and executive function in many ACC patients. We also confirmed and refined previously known CNVs, including significantly narrowing the 8p23.1-p11.1 duplication present in 2% of our current ACC cohort. We found six novel CNVs, each in a single patient, that are likely deleterious: deletions of 1p31.3-p31.1, 1q31.2-q31.3, 5q23.1, and 15q11.2-q13.1; and duplications of 2q11.2-q13 and 11p14.3-p14.2. One ACC patient with microcephaly had a paternally inherited deletion of 16p13.11 that included NDE1. Exome sequencing identified a recessive maternally inherited nonsense mutation in the non-deleted allele of NDE1, revealing the complexity of ACC genetics. This is the first systematic study of CNVs in congenital brain malformations, and shows a much higher prevalence of large gene-rich CNVs in ACC than in CBLH and PMG.

摘要

脑胼胝体发育不全(ACC)、小脑发育不良(CBLH)和多小脑回(PMG)是严重的先天性脑畸形,其病因在很大程度上尚未被发现。我们对 255 名 ACC、220 名 CBLH 和 147 名 PMG 患者以及 2349 名对照进行了大规模的染色体拷贝数变异(CNV)发现工作。与对照组相比,显著更多的 ACC 患者,而令人惊讶的是,CBLH 或 PMG 患者没有罕见的基因 CNV 超过 1 兆碱基(p=1.48×10⁻³;优势比[OR]=3.19;95%置信区间[CI]=1.89-5.39)。罕见的基因 CNV 是指影响不到患者和对照组合并人群中 1%的至少一个基因的 CNV。与对照组相比,显著更多的 ACC 患者,但不是 CBLH 或 PMG 患者,具有罕见的 CNV 影响超过 20 个基因(p=0.01;OR=2.95;95%置信区间[CI]=1.69-5.18)。独立的 qPCR 确认显示,9.4%的 ACC 患者存在新生 CNV。与遗传 CNV 相比,这些 CNV 优先与先前在自闭症谱系障碍患者中观察到的新生 CNV 重叠(p=3.06×10⁻⁴;OR=7.55;95%置信区间[CI]=2.40-23.72)。有趣的是,许多报告显示自闭症患者的胼胝体面积减小,许多 ACC 患者的社会和执行功能下降。我们还确认并细化了以前已知的 CNV,包括显著缩小了我们目前 ACC 队列中 2%存在的 8p23.1-p11.1 重复。我们发现了六个新的 CNV,每个患者一个,可能是有害的:1p31.3-p31.1、1q31.2-q31.3、5q23.1 和 15q11.2-q13.1 的缺失;以及 2q11.2-q13 和 11p14.3-p14.2 的重复。一名患有小头症的 ACC 患者存在父亲遗传的 16p13.11 缺失,其中包括 NDE1。外显子组测序在 NDE1 的非缺失等位基因中发现了一个母体隐性遗传的无意义突变,揭示了 ACC 遗传学的复杂性。这是先天性脑畸形中 CNV 的首次系统研究,显示 ACC 中基因丰富的大 CNV 的患病率明显高于 CBLH 和 PMG。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9905/3789824/d69aaafc8e47/pgen.1003823.g001.jpg

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