Piechaczyk M, Blanchard J M, Marty L, Dani C, Panabieres F, El Sabouty S, Fort P, Jeanteur P
Nucleic Acids Res. 1984 Sep 25;12(18):6951-63. doi: 10.1093/nar/12.18.6951.
We have isolated and identified cDNA clones containing part of the coding sequence for rat glyceraldehyde-3-phosphate-dehydrogenase (GAPDH, E.C. 1.2.1.12). By using one of these clones as a probe, we have shown that: i) the abundance of GAPDH mRNA is different in various tissues of the adult rat and in good correlation with the abundance of the enzyme; ii) the transcription rates are quite similar in all tissues tested. We therefore conclude that the tissue-specific differential GAPDH gene expression is regulated by adjusting the abundance of its mRNA at the post-transcriptional level.
我们已经分离并鉴定出包含大鼠甘油醛-3-磷酸脱氢酶(GAPDH,E.C. 1.2.1.12)部分编码序列的cDNA克隆。通过使用其中一个克隆作为探针,我们发现:i)成年大鼠不同组织中GAPDH mRNA的丰度不同,且与该酶的丰度密切相关;ii)在所有测试组织中,转录速率相当相似。因此我们得出结论,组织特异性的GAPDH基因差异表达是通过在转录后水平调节其mRNA的丰度来调控的。