TY - JOUR
T1 - Amino acid patterns within short consensus repeats define conserved duplicons shared by genes of the RCA complex
AU - Mcluire, C.A.
AU - Dawkins, R.L.
AU - Williamson, J.F.
AU - Davies, R.
AU - Berry, J.
AU - Gaudieri, S.
AU - Gaudieri, Silvana
PY - 2004
Y1 - 2004
N2 - Complement control proteins (CCPs) contain repeated protein domains, short consensus repeats (SCRs), which must be relevant to diverse functions such as complement activation, coagulation, viral binding, fetal implantation, and self-non-self recognition. Although SCRs share some discontinuous and imperfect motifs, there are many variable positions and indels making classification in subfamilies extremely difficult. Using domain-by-domain phylogenetic analysis, we have found that most domains can be classified into only 11 Subfamilies, designated a, b. c, d, e.. f, g h, i, j, or k and identified by critical residues. Each particular CCP is characterized by the order of representatives of the subfamilies. Human complement receptor I (CRI) has ajefbkd repeated four times and followed by ch. The classification crosses CCPs and indicates that a particular CCP is a function of the mix of SCRs. The aje set is a feature of several CCPs including human CRI and DAF and murine Crry and appears to be associated with the Success or failure of implantation inter (ilia. This approach facilitates genomic analysis of available sequences and suggests a framework for the evolution of CCPs. Units of duplication range from single SCRs, to septamers such as efbkdaj, to extensive segments such as MCP-CR1L. Imperfections of duplication with subsequent deletion have contributed to diversification.
AB - Complement control proteins (CCPs) contain repeated protein domains, short consensus repeats (SCRs), which must be relevant to diverse functions such as complement activation, coagulation, viral binding, fetal implantation, and self-non-self recognition. Although SCRs share some discontinuous and imperfect motifs, there are many variable positions and indels making classification in subfamilies extremely difficult. Using domain-by-domain phylogenetic analysis, we have found that most domains can be classified into only 11 Subfamilies, designated a, b. c, d, e.. f, g h, i, j, or k and identified by critical residues. Each particular CCP is characterized by the order of representatives of the subfamilies. Human complement receptor I (CRI) has ajefbkd repeated four times and followed by ch. The classification crosses CCPs and indicates that a particular CCP is a function of the mix of SCRs. The aje set is a feature of several CCPs including human CRI and DAF and murine Crry and appears to be associated with the Success or failure of implantation inter (ilia. This approach facilitates genomic analysis of available sequences and suggests a framework for the evolution of CCPs. Units of duplication range from single SCRs, to septamers such as efbkdaj, to extensive segments such as MCP-CR1L. Imperfections of duplication with subsequent deletion have contributed to diversification.
U2 - 10.1007/s00239-004-2609-8
DO - 10.1007/s00239-004-2609-8
M3 - Article
C2 - 15486690
SN - 0022-2844
VL - 59
SP - 143
EP - 157
JO - Journal of Molecular Evolution
JF - Journal of Molecular Evolution
IS - 2
ER -