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使用熔解曲线分析对肌强直性营养不良 1 型进行 CTG 重复扩增的高通量筛选。

High throughput screening for expanded CTG repeats in myotonic dystrophy type 1 using melt curve analysis.

机构信息

Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.

Department of Neurology, University of Utah, Salt Lake City, Utah, USA.

出版信息

Mol Genet Genomic Med. 2021 Apr;9(4):e1619. doi: 10.1002/mgg3.1619. Epub 2021 Feb 24.

Abstract

BACKGROUND

Myotonic dystrophy type 1 (DM1) is caused by CTG repeat expansions in the DMPK gene and is the most common form of muscular dystrophy. Patients can have long delays from onset to diagnosis, since clinical signs and symptoms are often nonspecific and overlapping with other disorders. Clinical genetic testing by Southern blot or triplet-primed PCR (TP-PCR) is technically challenging and cost prohibitive for population surveys.

METHODS

Here, we present a high throughput, low-cost screening tool for CTG repeat expansions using TP-PCR followed by high resolution melt curve analysis with saturating concentrations of SYBR GreenER dye.

RESULTS

We determined that multimodal melt profiles from the TP-PCR assay are a proxy for amplicon length stoichiometry. In a screen of 10,097 newborn blood spots, melt profile analysis accurately reflected the tri-modal distribution of common alleles from 5 to 35 CTG repeats, and identified the premutation and full expansion alleles.

CONCLUSION

We demonstrate that robust detection of expanded CTG repeats in a single tube can be achieved from samples derived from specimens with minimal template DNA such as dried blood spots (DBS). This technique is readily adaptable to large-scale testing programs such as population studies and newborn screening programs.

摘要

背景

1 型肌强直性营养不良(DM1)是由 DMPK 基因中的 CTG 重复扩展引起的,是最常见的肌肉疾病形式。由于临床体征和症状通常是非特异性的,并与其他疾病重叠,因此患者从发病到诊断可能会有很长的延迟。Southern 印迹或三重复引物 PCR(TP-PCR)的临床基因检测在技术上具有挑战性,并且对于人群调查来说成本过高。

方法

在这里,我们提出了一种使用 TP-PCR 进行高通量、低成本的 CTG 重复扩展筛选工具,然后使用高分辨率熔解曲线分析和饱和浓度的 SYBR GreenER 染料进行分析。

结果

我们确定,TP-PCR 检测的多峰熔解曲线是扩增子长度化学计量的替代物。在对 10097 个新生儿血斑进行筛查时,熔解曲线分析准确反映了 5 到 35 个 CTG 重复常见等位基因的三峰分布,并鉴定了前突变和全扩展等位基因。

结论

我们证明,从模板 DNA 最少的样本(如干血斑(DBS))中,可以在单个管中实现对扩展 CTG 重复的稳健检测。该技术易于适应大规模检测计划,如人群研究和新生儿筛查计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d55/8123750/2bb0b6e571a3/MGG3-9-e1619-g006.jpg

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