4.8 Article

Evolution of the AID/APOBEC family of polynucleotide (deoxy)cytidine deaminases

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MOLECULAR BIOLOGY AND EVOLUTION
卷 22, 期 2, 页码 367-377

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OXFORD UNIV PRESS
DOI: 10.1093/molbev/msi026

关键词

AID; APOBEC; antibody gene diversification; hypermutation; RNA editing; DNA deamination; immunity

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The AID/APOBEC family (comprising AID. APOBEC1 APOBEC2. and APOBEC3 subgroups) contains members that can deaminate cytidine in RNA and/or DNA and exhibit diverse physiological functions (AID and APOBEC3 deaminating DNA to trigger pathways in adaptive and innate immunity: APOBEC1 mediating apolipoprotein B RNA editing). The founder member APOBEC1, which has been used as a paradigm. is an RNA-editing enzyme with proposed antecedents in yeast. Here, we have undertaken phylogenetic analysis to glean insight into the primary physiological function of the AID/APOBEC family. We find that although the family forms part of a larger superfamily of deaminases distributed throughout the biological world, the AID/APOBEC family itself is restricted to vertebrates with homologs of AID (a DNA deaminase that triggers antibody gene diversification) and of APOBEC2 (unknown function) identifiable in sequence databases front bony fish, birds, amphibians, and mammals. The cloning of an AID homolog, from dogfish reveals that AID extends at least as far back as cartilaginous fish. Like mammalian AID. the pufferfish AID homolog, can trigger deoxycytidine deamination in DNA but, consistent with its cold-blooded origin, is thermolabile. The fine specificity of its mutator activity and the biased codon usage in pufferfish IgV genes appear broadly Similar to that of their mammalian counterparts, consistent with a coevolution of the antibody mutator and its substrate for the optimal targeting of somatic mutation during antibody maturation. By contrast, APOBEC1 and APOBEC3 are later evolutionary arrivals with orthologs not found in pufferfish (although synteny with mammals is maintained in respect of the flanking loci). We conclude that AID and APOBEC2 are likely to be the ancestral members of the AID/APOBEC family (going, back to the beginning of vertebrate speciation) with both APOBECI and A-POBEC3 being mammal-specific derivatives of AID and a complex set of domain shuffling underpinning the expansion and evolution of the primate APOBEC3s.

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