Finta C, Zaphiropoulos P G
Center for Nutrition and Toxicology, Department of Biosciences at NOVUM, Karolinska Institute, SE-14157, Huddinge, Sweden.
Gene. 2000 Dec 30;260(1-2):13-23. doi: 10.1016/s0378-1119(00)00470-4.
Using a bacterial artificial chromosome (BAC) clone, we have mapped the human cytochrome P450 3A (CYP3A) locus containing the genes encoding for CYP3A4, CYP3A5 and CYP3A7. The genes lie in a head-to-tail orientation in the order of 3A4, 3A7 and 3A5. In both intergenic regions (3A4-3A7 and 3A7-3A5), we have detected several additional cytochrome P450 3A exons, forming two CYP3A pseudogenes. These pseudogenes have the same orientation as the CYP3A genes. To our surprise, a 3A7 mRNA species has been detected in which the exons 2 and 13 of one of the pseudogenes (the one that is downstream of 3A7) are spliced after the 3A7 terminal exon. This results in an mRNA molecule that consists of the 13 3A7 exons and two additional exons at the 3' end. The additional two exons originating from the pseudogene are in an altered reading frame and consequently have the capability to code a completely different amino acid sequence than the canonical CYP3A exons 2 and 13. These findings may represent a generalized evolutionary process with genes having the potential to capture neighboring sequences and use them as functional exons.
利用细菌人工染色体(BAC)克隆,我们绘制了人类细胞色素P450 3A(CYP3A)基因座图谱,该基因座包含编码CYP3A4、CYP3A5和CYP3A7的基因。这些基因以头对尾的方向排列,顺序为3A4、3A7和3A5。在两个基因间隔区(3A4 - 3A7和3A7 - 3A5)中,我们检测到了几个额外的细胞色素P450 3A外显子,形成了两个CYP3A假基因。这些假基因与CYP3A基因具有相同的方向。令我们惊讶的是,检测到一种3A7 mRNA,其中一个假基因(3A7下游的那个)的外显子2和13在3A7末端外显子之后进行了剪接。这导致了一个mRNA分子,它由13个3A7外显子和3'端的另外两个外显子组成。源自假基因的另外两个外显子处于改变的阅读框中,因此能够编码与典型的CYP3A外显子2和13完全不同的氨基酸序列。这些发现可能代表了一个普遍的进化过程,即基因有可能捕获邻近序列并将其用作功能性外显子。