Evolution of a TRIM5-CypA splice isoform in old world monkeys

PLoS Pathog. 2008 Feb 29;4(2):e1000003. doi: 10.1371/journal.ppat.1000003.

Abstract

The TRIM family proteins share a conserved arrangement of three adjacent domains, an N-terminal RING domain, followed by one or two B-boxes and a coiled-coil, which constitutes the tripartite-motif for which the family is named. However, the C-termini of TRIM proteins vary, and include at least nine evolutionarily distinct, unrelated protein domains. Antiviral restriction factor TRIM5alpha has a C-terminal B30.2/SPRY domain, which is the major determinant of viral target specificity. Here, we describe the evolution of a cyclophilin-A encoding exon downstream of the TRIM5 locus of Asian macaques. Alternative splicing gives rise to chimeric transcripts encoding the TRIM motif fused to a C-terminal CypA domain (TRIM5-CypA). We detected TRIM5-CypA chimeric transcripts in primary lymphocytes from two macaque species. These were derived in part from a CypA pseudogene in the TRIM5 locus, which is distinct from the previously described CypA insertion in TRIM5 of owl monkeys. The CypA insertion is linked to a mutation in the 3' splice site upstream of exon 7, which may prevent or reduce expression of the alpha-isoform. All pig-tailed macaques (M. nemestrina) screened were homozygous for the CypA insertion. In contrast, the CypA-containing allele was present in 17% (17/101) of rhesus macaques (M. mulatta). The block to HIV-1 infection in lymphocytes from animals bearing the TRIM5-CypA allele was weaker than that in cells from wild type animals. HIV-1 infectivity remained significantly lower than SIV infectivity, but was not rescued by treatment with cyclosporine A. Thus, unlike owl monkey TRIMCyp, expression of the macaque TRIM5-CypA isoform does not result in increased restriction of HIV-1. Despite its distinct evolutionary origin, Macaca TRIM5-CypA has a similar domain arrangement and shares approximately 80% amino-acid identity with the TRIMCyp protein of owl monkeys. The independent appearance of TRIM5-CypA chimeras in two primate lineages constitutes a remarkable example of convergent evolution. Based on the presence of the CypA insertion in separate macaque lineages, and its absence from sooty mangabeys, we estimate that the Macaca TRIM5-CypA variant appeared 5-10 million years ago in a common ancestor of the Asian macaques. Whether the formation of novel genes through alternative splicing has played a wider role in the evolution of the TRIM family remains to be investigated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • Cercopithecidae
  • Cyclophilin A / genetics*
  • Cyclophilin A / metabolism
  • Evolution, Molecular*
  • Genotype
  • HIV Infections / genetics*
  • HIV Infections / immunology
  • HIV Infections / metabolism
  • HIV-1
  • Homozygote
  • Immunity, Innate
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Molecular Sequence Data
  • Monkey Diseases / genetics*
  • Monkey Diseases / immunology
  • Monkey Diseases / metabolism
  • Mutant Chimeric Proteins / genetics
  • Phytohemagglutinins / pharmacology
  • Polymorphism, Single Nucleotide
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Structure, Tertiary
  • Proteins / genetics*
  • Proteins / metabolism
  • Ubiquitin-Protein Ligases

Substances

  • Mutant Chimeric Proteins
  • Phytohemagglutinins
  • Protein Isoforms
  • Proteins
  • TRIM5(alpha) protein, rhesus monkey
  • Ubiquitin-Protein Ligases
  • Cyclophilin A

Associated data

  • GENBANK/EU359036
  • GENBANK/EU359037