Abstract:
:Factor VIII (antihemophilic factor) is a high molecular weight plasma glycoprotein that participates in the blood clotting cascade. The recent cloning and sequence analysis of the cDNA encoding human factor VIII revealed an obvious domain structure for the protein, which can be represented as A1-A2-B-A3-C1-C2. We now report the DNA sequence analysis of porcine exons encoding the entire B domain and part of the A2 and A3 domains. We found an unusually high degree of porcine-human amino acid sequence divergence in the B region compared with the limited sequence available for other regions of the porcine factor VIII molecule. In addition to sequence divergence, there are numerous gaps in the porcine B domain totalling over 200 amino acids. Recombinant DNA techniques were used to effect the removal of large segments of DNA encoding the B domain from the full-length human factor VIII cDNA. These constructs directed the synthesis of biologically active factor VIII when introduced into mammalian cells despite the deletion of up to 38% of the factor VIII molecule.
journal_name
Proc Natl Acad Sci U S Aauthors
Toole JJ,Pittman DD,Orr EC,Murtha P,Wasley LC,Kaufman RJdoi
10.1073/pnas.83.16.5939subject
Has Abstractpub_date
1986-08-01 00:00:00pages
5939-42issue
16eissn
0027-8424issn
1091-6490journal_volume
83pub_type
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