GSBS Student Publications

UMMS Affiliation

Graduate School of Biomedical Sciences; Department of Microbiology and Molecular Genetics; Department of Pathology

Date

4-5-2008

Document Type

Article

Medical Subject Headings

Amino Acid Sequence; Animals; B-Lymphocytes; Cercopithecidae; Cyclophilin A; *Evolution, Molecular; Genotype; HIV Infections; HIV-1; Homozygote; Immunity, Innate; Leukocytes, Mononuclear; Molecular Sequence Data; Monkey Diseases; Mutant Chimeric Proteins; Phytohemagglutinins; Polymorphism, Single Nucleotide; Protein Isoforms; Protein Structure, Tertiary; Proteins

Disciplines

Life Sciences | Medicine and Health Sciences

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.

Rights and Permissions

Citation: PLoS Pathog. 2008 Feb 29;4(2):e1000003. Link to article on publisher's site

Related Resources

Link to Article in PubMed

Journal Title

PLoS pathogens

PubMed ID

18389077

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