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Molecular characterization of the feline T-cell receptor ? alternate reading frame protein (TARP) ortholog.


ABSTRACT: T-cell receptor ? alternate reading frame protein (TARP) is expressed by human prostate epithelial, prostate cancer, and mammary cancer cells, but is not found in normal mammary tissue. To date, this protein has only been described in humans. Additionally, no animal model has been established to investigate the potential merits of TARP as tumor marker or a target for adoptive tumor immunotherapy. In this study conducted to characterize feline T-cell receptor ? sequences, constructs very similar to human TARP transcripts were obtained by RACE from the spleen and prostate gland of cats. Transcription of TARP in normal, hyperplastic, and neoplastic feline mammary tissues was evaluated by conventional RT-PCR. In felines similarly to the situation reported in humans, a C-region encoding two open reading frames is spliced to a J-region gene. In contrast to humans, the feline J-region gene was found to be a pseudogene containing a deletion within its recombination signal sequence. Our findings demonstrated that the feline TARP ortholog is transcribed in the prostate gland and mammary tumors but not normal mammary tissues as is the case with human TARP.

SUBMITTER: Weiss AT 

PROVIDER: S-EPMC3539119 | biostudies-literature | 2012 Dec

REPOSITORIES: biostudies-literature

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Molecular characterization of the feline T-cell receptor γ alternate reading frame protein (TARP) ortholog.

Weiss Alexander Th A AT   von Deetzen Marie-Charlotte MC   Hecht Werner W   Reinacher Manfred M   Gruber Achim D AD  

Journal of veterinary science 20121201 4


T-cell receptor γ alternate reading frame protein (TARP) is expressed by human prostate epithelial, prostate cancer, and mammary cancer cells, but is not found in normal mammary tissue. To date, this protein has only been described in humans. Additionally, no animal model has been established to investigate the potential merits of TARP as tumor marker or a target for adoptive tumor immunotherapy. In this study conducted to characterize feline T-cell receptor γ sequences, constructs very similar  ...[more]

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