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平面细胞极性基因之间的遗传相互作用导致小鼠出现多种神经管缺陷。

Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice.

机构信息

Centre for Biomedical Sciences, School of Biological Sciences, Royal Holloway University of London, Egham, TW20 0RD, UK. MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX11 0RD, UK.

MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX11 0RD, UK.

出版信息

Dis Model Mech. 2014 Oct;7(10):1153-63. doi: 10.1242/dmm.016758. Epub 2014 Aug 15.

Abstract

Neural tube defects (NTDs) are among the commonest and most severe forms of developmental defect, characterized by disruption of the early embryonic events of central nervous system formation. NTDs have long been known to exhibit a strong genetic dependence, yet the identity of the genetic determinants remains largely undiscovered. Initiation of neural tube closure is disrupted in mice homozygous for mutations in planar cell polarity (PCP) pathway genes, providing a strong link between NTDs and PCP signaling. Recently, missense gene variants have been identified in PCP genes in humans with NTDs, although the range of phenotypes is greater than in the mouse mutants. In addition, the sequence variants detected in affected humans are heterozygous, and can often be detected in unaffected individuals. It has been suggested that interactions between multiple heterozygous gene mutations cause the NTDs in humans. To determine the phenotypes produced in double heterozygotes, we bred mice with all three pairwise combinations of Vangl2(Lp), Scrib(Crc) and Celsr1(Crsh) mutations, the most intensively studied PCP mutants. The majority of double-mutant embryos had open NTDs, with the range of phenotypes including anencephaly and spina bifida, therefore reflecting the defects observed in humans. Strikingly, even on a uniform genetic background, variability in the penetrance and severity of the mutant phenotypes was observed between the different double-heterozygote combinations. Phenotypically, Celsr1(Crsh);Vangl2(Lp);Scrib(Crc) triply heterozygous mutants were no more severe than doubly heterozygous or singly homozygous mutants. We propose that some of the variation between double-mutant phenotypes could be attributed to the nature of the protein disruption in each allele: whereas Scrib(Crc) is a null mutant and produces no Scrib protein, Celsr1(Crsh) and Vangl2(Lp) homozygotes both express mutant proteins, consistent with dominant effects. The variable outcomes of these genetic interactions are of direct relevance to human patients and emphasize the importance of performing comprehensive genetic screens in humans.

摘要

神经管缺陷(NTDs)是最常见和最严重的发育缺陷形式之一,其特征是中枢神经系统形成的早期胚胎事件中断。NTDs 长期以来一直被认为具有很强的遗传依赖性,但遗传决定因素的身份在很大程度上仍未被发现。神经管闭合的启动在平面细胞极性(PCP)途径基因纯合突变的小鼠中受到干扰,为 NTDs 和 PCP 信号之间提供了强有力的联系。最近,在患有 NTDs 的人类中已鉴定出 PCP 基因中的错义基因突变,尽管表型范围大于小鼠突变体。此外,在受影响的人类中检测到的序列变异是杂合的,并且通常可以在未受影响的个体中检测到。有人认为,多个杂合基因突变的相互作用导致了人类的 NTDs。为了确定双杂合子产生的表型,我们将具有 Vangl2(Lp)、Scrib(Crc)和 Celsr1(Crsh)突变的所有三种双等位基因组合的小鼠进行杂交,这是研究最深入的 PCP 突变体。大多数双突变体胚胎的神经管缺陷是开放性的,表型范围包括无脑畸形和脊柱裂,因此反映了在人类中观察到的缺陷。引人注目的是,即使在统一的遗传背景下,不同双杂合子组合之间也观察到突变表型的外显率和严重程度存在差异。表型上,Celsr1(Crsh);Vangl2(Lp);Scrib(Crc)三重杂合突变体并不比双杂合或单纯合突变体更严重。我们提出,一些双突变体表型之间的差异可能归因于每个等位基因中蛋白破坏的性质:虽然 Scrib(Crc)是一个无效突变体,不产生 Scrib 蛋白,但 Celsr1(Crsh)和 Vangl2(Lp)纯合子都表达突变蛋白,符合显性效应。这些遗传相互作用的可变结果与人类患者直接相关,强调了在人类中进行全面遗传筛选的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b0/4174526/a36cec196b20/DMM016758F1.jpg

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