Nuclear localization signal in a cancer-related transcriptional regulator protein NAC1

作者：Okazaki Kosuke; Nakayama Naomi; Nariai Yuko; Nakayama Kentaro; Miyazaki Kohji; Maruyama Riruke; Kato Hiroaki; Kosugi Shunichi; Urano Takeshi^*; Sakashita Gyosuke

来源：Carcinogenesis, 2012, 33(10): 1854-1862.

DOI：10.1093/carcin/bgs193

Nucleus accumbens-associated protein 1 (NAC1) might have potential oncogenic properties and participate in regulatory networks for pluripotency. Although NAC1 is described as a transcriptional regulator, the nuclear import machinery of NAC1 remains unclear. We found, using a point mutant, that dimer formation was not committed to the nuclear localization of NAC1 and, using deletion mutants, that the amino-terminal half of NAC1 harbored a potential nuclear localization signal (NLS). Wild type, but not mutants of this region, alone was sufficient to drive the importation of green fluorescent protein (GFP) into the nucleus. Bimax1, a synthetic peptide that blocks the importin / pathway, impaired nuclear localization of NAC1 in cells. We also used the binding properties of importin to demonstrate that this region is an NLS. Furthermore, the transcriptional regulator function of NAC1 was dependent on its nuclear localization activity in cells. Taken together, these results show that the region with a bipartite motif constitutes a functional nuclear import sequence in NAC1 that is independent of NAC1 dimer formation. The identification of an NAC1 NLS thus clarifies the mechanism through which NAC1 translocates to the nucleus to regulate the transcription of genes involved in oncogenicity and pluripotency.

• 出版日期2012-10