INTRON EXON ORGANIZATION OF THE ACTIVE HUMAN PROTEIN-S GENE PS-ALPHA AND ITS PSEUDOGENE PS-BETA DUPLICATION AND SILENCING DURING PRIMATE EVOLUTION

The human protein S locus on chromosome 3 consists of two protein S genes, PSα and PSβ. Here we report the cloning and characterization of both genes. Fifteen exons of the PSα gene were identified that together code for protein S mRNA as derived from the reported protein S cDNAs. Analysis by primer extension of liver protein S mRNA, however, reveals the presence of two mRNA forms that differ in the length of their 5′-noncoding region. Both transcripts contain a 5′-noncoding region longer than found in the protein S cDNAs. The two products may arise from alternative splicing of an additional intron in this region or from the usage of two start sites for transcription. The intron-exon organization of the PSa gene fully supports the hypothesis that the protein S gene is the product of an evolutional assembling process in which gene modules coding for structural/functional protein units also found in other coagulation proteins have been put upstream of the ancestral gene of a steroid hormone binding protein. The PSβ gene is identified as a pseudogene. It contains a large variety of detrimental aberrations, viz., the absence of exon I, a splice site mutation, three stop codons, and a frame shift mutation. Overall, the two genes PSα and PSβ show between their exonic sequences 96.5% homology. Southern analysis of primate DNA showed that the duplication of the ancestral protein S gene has occurred after the branching of the orangutan from the African apes. A nonsense mutation that is present in the pseudogene of man also could be identified in one of the two protein S genes of both chimpanzee and gorilla. This implicates that silencing of one of the two protein S genes must have taken place before the divergence of the three African apes. © 1990, American Chemical Society. All rights reserved.