Douthart R J, Norris F H
Science. 1982 Aug 20;217(4561):729-32. doi: 10.1126/science.7100918.
An extensive computer-assisted analysis of known pre-proinsulin coding sequences has shown correlations that can be interpreted as evidence for an intron-mediated juxtaposition of exons in the evolution of these genes. The evidence includes the discovery that the regions of the pre-proinsulin genes that code for the signal peptide consist of nearly tandem repeating units of nine base pairs. This pattern reappears in the C region of the genes after a large intron that occurs in three of the four genes analyzed. A model is proposed in which primordial insulin was coded for by two separate minigenes arising from a gene duplication, each with identical or nearly identical signal peptide coding regions. The minigenes fused into one transcriptional unit mediated by the large intron, and the signal peptide coding region of one of the putative minigenes evolved into the latter portion of the C peptide coding region.
对已知的胰岛素原前体编码序列进行的广泛计算机辅助分析显示了一些相关性,这些相关性可被解释为这些基因进化过程中外显子通过内含子介导并置的证据。证据包括发现胰岛素原前体基因中编码信号肽的区域由九个碱基对的近乎串联重复单元组成。在分析的四个基因中的三个基因中出现的一个大内含子之后,这种模式在基因的C区域再次出现。提出了一个模型,其中原始胰岛素由基因复制产生的两个单独的小基因编码,每个小基因具有相同或几乎相同的信号肽编码区域。这些小基因通过大内含子融合成一个转录单元,并且其中一个假定小基因的信号肽编码区域进化为C肽编码区域的后半部分。