Kawaguchi Kosuke, Okamoto Takumi, Morita Masashi, Imanaka Tsuneo
Department of Biological Chemistry, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Sci Rep. 2016 Jul 26;6:30183. doi: 10.1038/srep30183.
We previously demonstrated that ABCD4 does not localize to peroxisomes but rather, the endoplasmic reticulum (ER), because it lacks the NH2-terminal hydrophilic region required for peroxisomal targeting. It was recently reported that mutations in ABCD4 result in a failure to release vitamin B12 from lysosomes. A similar phenotype is caused by mutations in LMBRD1, which encodes the lysosomal membrane protein LMBD1. These findings suggested to us that ABCD4 translocated from the ER to lysosomes in association with LMBD1. In this report, it is demonstrated that ABCD4 interacts with LMBD1 and then localizes to lysosomes, and this translocation depends on the lysosomal targeting ability of LMBD1. Furthermore, endogenous ABCD4 was localized to both lysosomes and the ER, and its lysosomal localization was disturbed by knockout of LMBRD1. To the best of our knowledge, this is the first report demonstrating that the subcellular localization of the ABC transporter is determined by its association with an adaptor protein.
我们之前证明,ABCD4并不定位于过氧化物酶体,而是定位于内质网(ER),因为它缺乏过氧化物酶体靶向所需的NH2末端亲水区域。最近有报道称,ABCD4中的突变导致无法从溶酶体中释放维生素B12。编码溶酶体膜蛋白LMBD1的LMBRD1中的突变也会导致类似的表型。这些发现让我们推测,ABCD4与LMBD1结合后从内质网转移至溶酶体。在本报告中,我们证明ABCD4与LMBD1相互作用,然后定位于溶酶体,并且这种转移取决于LMBD1的溶酶体靶向能力。此外,内源性ABCD4定位于溶酶体和内质网,LMBRD1基因敲除会干扰其溶酶体定位。据我们所知,这是第一份证明ABC转运蛋白的亚细胞定位由其与衔接蛋白的结合所决定的报告。