Quantitative gene expression analysis in renal biopsies:: A novel protocol for a high-throughput multicenter application

被引:229
|
作者
Cohen, CD [1 ]
Frach, K [1 ]
Schlöndorff, D [1 ]
Kretzler, M [1 ]
机构
[1] Univ Munich, Med Poliklin, D-80336 Munich, Germany
关键词
real-time RT-PCR; lab-on-a-chip; RNase inhibitor; RNA isolation; microdissection;
D O I
10.1046/j.1523-1755.2002.00113.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Recent advances in gene expression analysis may add the quantification of mRNA species in renal biopsies to routine diagnostic procedures in nephrology. Methods. A systematic evaluation was performed on the relevant steps required to efficiently obtain cDNA from renal biopsies for high-throughput reverse transcription-polymerase chain reaction (RT-PCR) based mRNA quantification. Results. The protocol preserves mRNA integrity by a novel RNase inhibitor and allows meticulous microdissection followed by maximal RNA recovery from tissue samples. Reverse transcription was optimized to give the best yield from minimal starting material. RNA quantity and quality were systematically investigated by real-time RT-PCR and electrophoresis on a microfluidic system, respectively. The reported procedure offers high RNA preservation and increases the yield of cDNA significantly compared to former protocols. Conclusion. The simplicity of biopsy material acquisition combined with the centrally performed processing makes this protocol suitable for a wide spectrum of expression analysis in diverse clinical settings.
引用
收藏
页码:133 / 140
页数:8
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