Abstract
Thirty thousand colonies of a bovine liver cDNA library were screened with a mixture of synthetic oligodeoxyribonucleotides coding for bovine factor X. Five positive colonies were identified, and plasmid DNA was isolated. Cleavage with restriction endonucleases showed that these plasmids (designated pBX1 -5) contained inserts of 1530bp , 770bp , 700bp , 1100bp and 930bp . DNA sequence analysis of the plasmid with the largest insert ( pBX1 ) confirmed that bovine factor X cDNAs had been cloned. The cDNA sequence predicts that factor X is synthesized as a single chain precursor in which the light and heavy chains of plasma factor X are linked by the dipeptide Arg-Arg. The cDNA sequence also predicts that factor X is synthesized with a prepro leader peptide. We propose that at least five specific proteolytic events occur during the conversion of prepro -factor X to plasma factor Xa.
MeSH Terms
Amino Acid Sequence
Animals
Base Sequence
Cattle
Cloning, Molecular
DNA/analysis
DNA Restriction Enzymes
Factor IX/genetics
Factor X/genetics
Genes
Humans
Oligodeoxyribonucleotides/genetics
Protein Precursors/genetics
Prothrombin/genetics
RNA, Messenger/genetics
Chemicals
Oligodeoxyribonucleotides
Protein Precursors
RNA, Messenger
Prothrombin
Factor IX
Factor X
DNA
DNA Restriction Enzymes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fung M R
Campbell R M
MacGillivray R T
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23 references, click to expand
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