Reid K B
Immunology. 1985 Jun;55(2):185-96.
The isolation of cDNA and, in certain cases, genomic clones has been reported for the following complement proteins: C1q, C2, C3, C4, C5, C9, and factor B, C4b-binding protein and C1-inhibitor. The availability of cloned DNA has allowed rapid advances to be made in the understanding of the structure (from the derived amino acid sequences), function, biosynthesis and genetics of these proteins. This is most strongly illustrated from recent studies on the C2, factor B and C4 genes, which code for the class III molecules of the major histocompatibility complex, especially as certain allelic forms of these genes may be associated with disease susceptibility.
已报道从下列补体蛋白中分离出了cDNA,在某些情况下还分离出了基因组克隆:C1q、C2、C3、C4、C5、C9、B因子、C4b结合蛋白和C1抑制因子。克隆DNA的可得性使得在理解这些蛋白质的结构(从推导的氨基酸序列)、功能、生物合成和遗传学方面取得了迅速进展。对C2、B因子和C4基因的最新研究最有力地说明了这一点,这些基因编码主要组织相容性复合体的III类分子,特别是因为这些基因的某些等位基因形式可能与疾病易感性有关。