Human α2-HS-glycoprotein: The A and B chains with a connecting sequence are encoded by a single mRNA transcript

C. C. Lee, B. H. Bowman, F. Yang

Research output: Contribution to journalArticlepeer-review

85 Scopus citations


The α2-HS-glycoprotein (AHSG) in a plasma protein reported to play roles in bone mineralization and in the immune response. It is composed of two subunits, the A and B chains. Recombinant plasmids containing human cDNA AHSG have been isolated by screening an adult human liver library with a mixed oligonucleotide probe. The cDNA clones containing AHSG inserts span approximately 1.5 kilobase pairs and include the entire AHSG coding sequence, demonstrating that the A and B chains are encoded by a single mRNA transcript. The cDNA sequence predicts an 18-amino-acid signal peptide, followed by the A-chain sequence of AHSG. A heretofore unseen connecting sequence of 40 amino acids are deduced between the A- and B-chain sequences. The connecting sequence demonstrates the unique amino acid doublets and collagen triplets found in the A and B chains; it is not homologous with other reported amino acid sequences. The connecting sequence may be cleaved in a posttranslational step by limited proteolysis before mature AHSG is released into the circulation or may vary in its presence because of alternative processing. The AHSG cDNA was utilized for mapping the AHSG gene to the 3q21→qter region of human chromosome 3. The availability of the AHSG cDNA clone will facilitate the analysis of its genetic control and gene expression during development and bone formation.

Original languageEnglish (US)
Pages (from-to)4403-4407
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number13
StatePublished - 1987
Externally publishedYes

ASJC Scopus subject areas

  • General


Dive into the research topics of 'Human α2-HS-glycoprotein: The A and B chains with a connecting sequence are encoded by a single mRNA transcript'. Together they form a unique fingerprint.

Cite this