A Ufd2/D4Cole1e chimeric protein and overexpression of Rbp7 in the slow Wallerian degeneration (Wld^s) mouse

Conforti, Laura, Tarlton, Andrea, Mack, Till G.A., Mi, Weiqian, Buckmaster, E. Anne, Wagner, Diana, Perry, V. Hugh and Coleman, Michael P. (2000) A Ufd2/D4Cole1e chimeric protein and overexpression of Rbp7 in the slow Wallerian degeneration (Wld^s) mouse. Proceedings of the National Academy of Sciences of the United States of America, 97 (21), 11377-11382. (doi:10.1073/pnas.97.21.11377).

Abstract

Exons of three genes were identified within the 85-kilobase tandem triplication unit of the slow Wallerian degeneration mutant mouse, C57BL/Wld^s). Ubiquitin fusion degradation protein 2 (Ufd2) and a previously undescribed gene, D4Cole1e, span the proximal and distal boundaries of the repeat unit, respectively. They have the same chromosomal orientation and form a chimeric gene when brought together at the boundaries between adjacent repeat units in Wld^s. The chimeric mRNA is abundantly expressed in the nervous system and encodes an in-frame fusion protein consisting of the N-terminal 70 amino acids of Ufd2, the C-terminal 302 amino acids of D4Cole1e, and an aspartic acid formed at the junction. Antisera raised against synthetic peptides detect the expected 43-kDa protein specifically in Wld^s brain. This expression pattern, together with the previously established role of ubiquitination in axon degeneration, makes the chimeric gene a promising candidate for Wld. The third gene altered by the triplication, Rbp7, is a novel member of the cellular retinoid-binding protein family and is highly expressed in white adipose tissue and mammary gland. The whole gene lies within the repeat unit leading to overexpression of the normal transcript in Wld^s mice. However, it is undetectable on Northern blots of Wld^s brain and seems unlikely to be the Wld gene. These data reveal both a candidate gene for Wld and the potential of the Wld^s mutant for studies of ubiquitin and retinoid metabolism.

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