Housekeeping genes as internal standards: use and limits

被引:1248
作者
Thellin, O
Zorzi, W
Lakaye, B
De Borman, B
Coumans, B
Hennen, G
Grisar, T
Igout, A
Heinen, E
机构
[1] Univ Liege, Inst Human Histol, B-4020 Liege, Belgium
[2] Univ Liege, Lab Biochem Endocrinol, B-4020 Liege, Belgium
[3] Univ Liege, Biochem Lab, Res Grp Neurochem, B-4020 Liege, Belgium
关键词
internal standards; housekeeping genes; RNase protection; RT-PCR;
D O I
10.1016/S0168-1656(99)00163-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Quantitative studies are commonly realised in the biomedical research to compare RNA expression in different experimental or clinical conditions. These quantifications are performed through their comparison to the expression of the housekeeping gene transcripts like glyceraldehyde-3-phosphate dehydrogenase (G3PDH), albumin, actins, tubulins, cyclophilin, hypoxantine phosphoribosyltransferase (HRPT), L32. 28S and 18S rRNAs are also used as internal standards. In this paper, it is recalled that the commonly used internal standards can quantitatively vary in response to various factors. Possible variations are illustrated using three experimental examples. Preferred types of internal standards are then proposed for each of these samples and thereafter the general procedure concerning the choice of an internal standard and the way to manage its used are discussed. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:291 / 295
页数:5
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