Molecular basis of hereditary C1q deficiency.

Article Details

Citation

Petry F

Molecular basis of hereditary C1q deficiency.

Immunobiology. 1998 Aug;199(2):286-94.

PubMed ID
9777412 [ View in PubMed
]
Abstract

Complete selective deficiencies of the complement component C1q are rare genetic disorders which are associated with recurrent infections and a high prevalence of lupus erythematosus-like symptoms. The improvements in molecular biology techniques have facilitated the analysis of such genetic defects to a great extend. To date the basis of C1q deficiencies from 13 families have been studied at the genetic level. In each case single base mutations leading to either termination codons, frame shift or amino acid exchanges were thought to be responsible for these defects as no other aberrations were found. In addition to DNA analysis, conventional immunochemical and biochemical methods have contributed substantially to the elucidation of the structural and functional requirements of this complex macromolecule. The present article reviews the different types of C1q defects in regard to structure and function whereas a detailed presentation on the clinical aspects of C1q deficiencies will be given in this issue of the Journal (by WALPORT, DAVIES and BOTTO).

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Complement C1q subcomponent subunit AP02745Details
Complement C1q subcomponent subunit BP02746Details
Complement C1q subcomponent subunit CP02747Details