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分子诊断学

Molecular diagnostics.

作者信息

Wagener C

机构信息

Abteilung für Klinische Chemie, Medizinische Klinik, Universitätskrankenhaus Eppendorf, Hamburg, Germany.

出版信息

J Mol Med (Berl). 1997 Oct;75(10):728-44. doi: 10.1007/s001090050159.

DOI:10.1007/s001090050159
PMID:9382997
Abstract

Nucleic acid technology has assumed an essential role in various areas of in vitro diagnosis. Its major applications include the genomic characterization of mutations and polymorphisms, amplification of nucleic acids by the polymerase chain reaction, analysis of gene expression patterns at the mRNA level, specific detection of mutant proteins, and engineering of proteins used in ligand binding assay. Manipulating the expression of genes in cells and experimental animals allows detailed analysis of processes leading from genomic alterations to disease manifestations and may ultimately yield refinements in diagnostic strategies. The addition of DNA and RNA to the conventional diagnostic in vitro targets and novel approaches to the study of disease processes and manifestations characterize a diagnostic strategy referred to as "molecular diagnostics." This contribution describes some of essential ways in which molecular diagnostics differs from conventional diagnostic approaches. Applications such as differential diagnosis, prenatal diagnosis, early diagnosis, and diagnosis of disease susceptibility are well established in single-gene disorders, and the diagnostic impact of DNA polymorphisms is steadily increasing in multifactorial diseases. The high sensitivity of the polymerase chain reaction makes possible the detection of single infectious agents or tumor cells. With increasing knowledge of expressed gene sequences the expression pattern of mRNA will reflect the biological state of cells with high precision. Mutant proteins can be analyzed based on their structural or biological properties. Use of the appropriate expression systems makes it possible to design proteins for diagnostic in vitro applications such as ligand binding assays.

摘要

核酸技术在体外诊断的各个领域都发挥着重要作用。其主要应用包括突变和多态性的基因组特征分析、通过聚合酶链反应扩增核酸、在mRNA水平分析基因表达模式、特异性检测突变蛋白以及用于配体结合测定的蛋白质工程。在细胞和实验动物中操纵基因表达,可以详细分析从基因组改变到疾病表现的过程,最终可能会改进诊断策略。将DNA和RNA添加到传统的体外诊断靶点中,以及研究疾病过程和表现的新方法,构成了一种被称为“分子诊断”的诊断策略。本文介绍了分子诊断与传统诊断方法不同的一些重要方面。诸如鉴别诊断、产前诊断、早期诊断和疾病易感性诊断等应用在单基因疾病中已得到充分确立,并且DNA多态性在多因素疾病中的诊断作用正在稳步增加。聚合酶链反应的高灵敏度使得检测单个感染因子或肿瘤细胞成为可能。随着对表达基因序列的了解不断增加,mRNA的表达模式将高精度地反映细胞的生物学状态。突变蛋白可以根据其结构或生物学特性进行分析。使用合适的表达系统可以设计用于体外诊断应用(如配体结合测定)的蛋白质。

相似文献

1
Molecular diagnostics.分子诊断学
J Mol Med (Berl). 1997 Oct;75(10):728-44. doi: 10.1007/s001090050159.
2
Diagnosis at the bedside by gene analysis.通过基因分析进行床边诊断。
South Med J. 1990 Aug;83(8):868-75. doi: 10.1097/00007611-199008000-00005.
3
[DNA-based diagnosis].
Orv Hetil. 1990 May 6;131(18):953-6, 959-64.
4
DNA chip technology ante portas.DNA芯片技术即将问世。
J Mol Med (Berl). 1999 Nov;77(11):761-8. doi: 10.1007/s001099900057.
5
[The amplification of nucleotide sequences by PCR and the new technics for molecular diagnosis].[通过聚合酶链反应(PCR)扩增核苷酸序列及分子诊断新技术]
Reprod Nutr Dev. 1990;Suppl 1:117s-124s.
6
The polymerase chain reaction. A revolution in clinical diagnostic procedures.聚合酶链反应。临床诊断程序的一场革命。
Acta Clin Belg. 1990;45(2):71-7. doi: 10.1080/17843286.1990.11735714.
7
Amplification of sequences from affected individuals.对患病个体的序列进行扩增。
Curr Protoc Hum Genet. 2001 May;Chapter 7:Unit 7.1. doi: 10.1002/0471142905.hg0701s00.
8
Principles and applications of the polymerase chain reaction.聚合酶链反应的原理与应用
J Int Fed Clin Chem. 1993 Jul;5(3):96-105.
9
Clinical impact of molecular diagnostics in endocrinology. Polymorphisms, mutations and DNA technologies.
Horm Res. 2002;58 Suppl 3:7-15. doi: 10.1159/000066477.
10
An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.一种通过分析扩增的DNA序列进行遗传性疾病产前诊断的改进方法。应用于甲型血友病。
N Engl J Med. 1987 Oct 15;317(16):985-90. doi: 10.1056/NEJM198710153171603.

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