Characterization of the gene for human plasminogen, a key proenzyme in the fibrinolytic system

• Published in: The Journal of biological chemistry Vol. 265; no. 11; pp. 6104 - 6111
• Main Authors: PETERSEN, T. E, MARTZEN, M. R, ICHINOSE, A, DAVIE, E. W
• Format: Journal Article
• Language: English
• Published: Bethesda, MD American Society for Biochemistry and Molecular Biology 15.04.1990
• Subjects: Amino Acid Sequence; Base Sequence; Biological and medical sciences; Codon - genetics; Enzyme Precursors - genetics; Exons; Fibrinogen - genetics; Fibrinolysis; Fundamental and applied biological sciences. Psychology; Gene Amplification; Gene Library; Genes; Genes. Genome; Humans; Introns; leucocytes; Macromolecular Substances; Molecular and cellular biology; Molecular genetics; Molecular Sequence Data; Oligonucleotide Probes; Protein Conformation; Restriction Mapping; Sequence Homology, Nucleic Acid; Human; Gene amplification; Nucleotide sequence; Gene organization; Plasminogen; Apolipoproteins; In vitro; Intervening sequence; Aminoacid sequence
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/s0021-9258(19)39298-1

The organization and structure of the gene coding for plasminogen has been determined by a combination of in vitro amplification of leukocyte DNA from normal individuals and isolation of unique clones from three different human genomic libraries. These clones were characterized by restriction mapping, Southern blotting, and DNA sequencing. The gene for human plasminogen spanned about 52.5 kilobases of DNA and consisted of 19 exons separated by 18 introns. DNA sequence analysis revealed that the five kringle structures in plasminogen were coded by two exons. The nucleotides in the introns at the intron-exon boundaries were GT-AG analogous to those found in other eukaryotic genes. Three polyadenylation sites for plasminogen mRNA were also identified. When the amino acid sequences deduced from the genomic DNA and cDNAs of plasminogen were compared with that of the plasma protein determined by amino acid sequence analysis, an apparent amino acid polymorphism was observed in several positions of the polypeptide chain. Nucleotide sequence analysis of the amplified genomic DNAs and genomic clones also revealed that the plasminogen gene was very closely related to several other proteins, including apolipoprotein(a). This protein may have evolved via duplication and exon shuffling of the plasminogen gene. The presence of another plasminogen-related gene(s) in the human genomic library was also observed.