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用于少量DNA材料拷贝数分析的多重连接依赖探针扩增技术。

Multiplex ligation-dependent probe amplification technique for copy number analysis on small amounts of DNA material.

作者信息

Sørensen Karina Meden, Andersen Paal Skytt, Larsen Lars Allan, Schwartz Marianne, Schouten Jan P, Nygren Anders O H

机构信息

National Center for Antimicrobials and Infection Control, Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen S, Denmark.

出版信息

Anal Chem. 2008 Dec 1;80(23):9363-8. doi: 10.1021/ac801688c.

Abstract

The multiplex ligation-dependent probe amplification (MLPA) technique is a sensitive technique for relative quantification of up to 50 different nucleic acid sequences in a single reaction, and the technique is routinely used for copy number analysis in various syndromes and diseases. The aim of the study was to exploit the potential of MLPA when the DNA material is limited. The DNA concentration required in standard MLPA analysis is not attainable from dried blood spot samples (DBSS) often used in neonatal screening programs. A novel design of MLPA probes has been developed to permit for MLPA analysis on small amounts of DNA. Six patients with congenital adrenal hyperplasia (CAH) were used in this study. DNA was extracted from both whole blood and DBSS and subjected to MLPA analysis using normal and modified probes. Results were analyzed using GeneMarker and manual Excel analysis. A total number of 792 ligation events were analyzed. In DNA extracted from dried blood spot samples, 99.1% of the results were accurate compared to 99.9% of the results obtained in DNA from whole blood samples. This study clearly demonstrates that MLPA reactions with modified probes are successful and reliable with DNA concentrations down to 0.3 ng/microL (1.6 ng total). This broadens the diagnostic perspectives of samples of DBSS allowing for copy number variation analysis in general and particularly testing for CAH.

摘要

多重连接依赖探针扩增(MLPA)技术是一种灵敏的技术,可在单次反应中对多达50种不同的核酸序列进行相对定量,该技术常规用于各种综合征和疾病的拷贝数分析。本研究的目的是在DNA材料有限时发挥MLPA的潜力。标准MLPA分析所需的DNA浓度无法从新生儿筛查项目中常用的干血斑样本(DBSS)中获得。已开发出一种新型的MLPA探针设计,以允许对少量DNA进行MLPA分析。本研究使用了6例先天性肾上腺皮质增生症(CAH)患者。从全血和DBSS中提取DNA,并使用正常探针和改良探针进行MLPA分析。使用GeneMarker和手动Excel分析对结果进行分析。共分析了792次连接事件。在从干血斑样本中提取的DNA中,99.1%的结果是准确的,而从全血样本DNA中获得的结果准确率为99.9%。本研究清楚地表明,使用改良探针的MLPA反应在DNA浓度低至0.3 ng/μL(总量1.6 ng)时是成功且可靠的。这拓宽了DBSS样本的诊断前景,使得一般的拷贝数变异分析成为可能,特别是对CAH的检测。

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