-transparent.png){kind=logo}
Human complement component C4b-binding protein (C4BP) is composed of seven alpha-chains and one beta-chain. The alpha- and beta-chains are homologous and both contain multiple copies of short consensus repeats (SCR) and in addition carboxyl-terminal non-repeat regions. Each of the alpha-chains contains a binding site for C4b, whereas the beta-chain binds protein S, a vitamin K-dependent protein involved in the regulation of blood coagulation. The alpha- and beta-chain genes are closely linked in the regulators of complement activation gene cluster on the long arm of human chromosome 1, band 1q32. The human beta-chain gene which has now been characterized was found to span more than 10 kilobases of DNA. The presence of at least two different beta-chain gene transcripts was suggested by the isolation of two new cDNA clones which contained different sequences in their extended 5'-untranslated regions. Northern blot analysis demonstrated that the two clones represented distinct beta-chain mRNAs with different 5' end sequences. One class of beta-chain mRNA (denoted A19) was found to be encoded by six exons and primer extension, and S1 nuclease protection assays revealed multiple closely spaced transcription start sites for this mRNA class. Its 5'-untranslated region and signal peptide was encoded by the first exon. The second class of mRNA (denoted A12) had a different transcription start site and its 5'-untranslated region was derived from at least three exons out of which the last one was formed by utilization of an acceptor splice site within the first A19 exon. Exons encoding the mature beta-chain and the 3'-untranslated region were common to both classes of mRNA. The beta-chain contains three SCRs, out of which the first and second are encoded by individual exons, whereas two exons encode the third SCR. The exon encoding the carboxyl-terminal part of the third SCR also encodes 14 amino acids of the non-repeat region. The last exon encodes the remaining 46 carboxyl-terminal amino acids and the entire 3'-untranslated region. The elucidation of the organization of the beta-chain gene provides insight into the sophisticated molecular structure of C4BP and a basis for future structural and functional studies.
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
January 1991,
Scandinavian journal of clinical and laboratory investigation. Supplementum,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
January 1991,
Biochemical and biophysical research communications,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
October 1990,
Thrombosis and haemostasis,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
September 1999,
European journal of cell biology,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
January 1994,
The Journal of biological chemistry,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
August 1996,
The Journal of biological chemistry,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
June 1995,
The Biochemical journal,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
June 1994,
Genomics,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
August 1986,
FEBS letters,
A Hillarp, and
F Pardo-Manuel, and
R R Ruiz, and
S Rodriguez de Cordoba, and
B Dahlbäck
February 1990,
Proceedings of the National Academy of Sciences of the United States of America,
