The three heavy-chain precursors for the inter-alpha-inhibitor family in mouse: new members of the multicopper oxidase protein group with differential transcription in liver and brain
Autor: | G Raguenez, J L Risler, Jean-Philippe Salier, P Chan |
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Jazyk: | angličtina |
Rok vydání: | 1995 |
Předmět: |
DNA
Complementary Transcription Genetic Molecular Sequence Data Sequence Homology Biology Multicopper oxidase Biochemistry Polymerase Chain Reaction Mice Transcription (biology) Alpha-Globulins von Willebrand Factor Animals Humans Amino Acid Sequence RNA Messenger Protein Precursors Alpha globulin Molecular Biology Gene Peptide sequence Brain Chemistry Multiple sequence alignment Base Sequence cDNA library Oligonucleotide Brain RNA-Directed DNA Polymerase Cell Biology Molecular biology Liver Oxidoreductases Research Article |
Popis: | The inter-alpha-inhibitor (I alpha I) family is comprised of the plasma protease inhibitors I alpha I, inter-alpha-like inhibitor (I alpha LI), pre-alpha-inhibitor (P alpha I) and bikunin. I alpha I, I alpha LI and P alpha I are distinct assemblies of bikunin with one of three heavy (H) chains designated H1, H2 and H3. These H chains and bikunin are respectively encoded by a set of three H genes and an alpha 1-microglobulin/bikunin precursor (AMBP) gene. All four gene products undergo maturation steps from precursor polypeptides. The full-length cDNAs for the H1-, H2- and H3-chain precursors were cloned from a mouse liver cDNA library and sequenced. Extensive searches of amino acid sequence similarities to other proteins in databanks revealed (i) a highly significant similarity of the C-terminal sequence in the three H-chain precursors to the multicopper-binding domain in the group of multicopper oxidase proteins and (ii) the presence of von Willebrand type-A domains in the mature H chains. Amino acid sequence comparisons between the three mouse H1-, H2- and H3-chain precursors and their human counterparts allowed us to appraise the timing and order of occurrence of the three H-chain genes from a shared ancestor during mammalian evolution. Owing to a multiple alignment of the six mouse and human nucleotide sequences for these H-chain precursors, a reverse transcriptase PCR assay with degenerate oligonucleotides was designed, allowing us to (i) present evidence that no mRNAs for further H genes exist in mouse liver and (ii) demonstrate a previously undescribed transcription of the H2- and H3-chain mRNAs in mouse brain, which contrasts with the expression of all four, H1, H2, H3 and AMBP, mRNAs in liver. |
Databáze: | OpenAIRE |
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