Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 293, Issue 16, Pages 5847-5859Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.RA117.000972
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Funding
- National Natural Science Foundation of China [81320108023, 81600171, 81770215]
- Priority Academic Program Development of Jiangsu Higher Education Institutions
- Jiangsu Key Laboratory for Neuropsychiatric Diseases Grant [BK2013003]
- Suzhou Key Laboratory for Pediatric Leukemia Grant [SZS201615]
- Suzhou Key Medical Center Grant [Szzx201506]
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TMEPAI (transmembrane prostate androgen-induced protein, also called prostate transmembrane protein, androgen-induced 1 (PMEPA1)) is a type I transmembrane (TM) protein, but its cellular function is largely unknown. Here, studying factors influencing the stability of c-Maf, a critical transcription factor in multiple myeloma (MM), we found that TMEPAI induced c-Maf degradation. We observed that TMEPAI recruited NEDD4 (neural precursor cell expressed, developmentally down-regulated 4), aWWdomain-containing ubiquitin ligase, to c-Maf, leading to its degradation through the proteasomal pathway. Further investigation revealed that TMEPAI interacts with NEDD4 via its conserved PY motifs. Alanine substitution or deletion of these motifs abrogated the TMEPAI complex formation with NEDD4, resulting in failed c-Maf degradation. Functionally, TMEPAI suppressed the transcriptional activity of c-Maf. Of note, increased TMEPAI expression was positively associated with the overall survival of MM patients. Moreover, TMEPAI was down-regulated in MMcells, and re-expression of TMEPAI induced MM cell apoptosis. In conclusion, this study highlights that TMEPAI decreases c-Maf stability by recruiting the ubiquitin ligase NEDD4 to c-Maf for proteasomal degradation. Our findings suggest that the restoration of functional TMEPAI expression may represent a promising complementary therapeutic strategy for treating patients with MM.
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