Journal
NATURE GENETICS
Volume 44, Issue 10, Pages 1152-+Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/ng.2386
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Funding
- Swiss National Science Foundation [320000_122568, 31003A_138521]
- Deutsche Forschungsgemeinschaft [RU816/5-1]
- Canadian Institutes for Health Research [15078]
- Swiss National Science Foundation (SNF) [31003A_138521] Funding Source: Swiss National Science Foundation (SNF)
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Inherited disorders of vitamin B-12 (cobalamin) have provided important clues to how this vitamin, which is essential for hematological and neurological function, is transported and metabolized. We describe a new disease that results in failure to release vitamin B-12 from lysosomes, which mimics the cblF defect caused by LMBRD1 mutations. Using microcell-mediated chromosome transfer and exome sequencing, we identified causal mutations in ABCD4, a gene that codes for an ABC transporter, which was previously thought to have peroxisomal localization and function. Our results show that ABCD4 colocalizes with the lysosomal proteins LAMP1 and LMBD1, the latter of which is deficient in the cblF defect. Furthermore, we show that mutations altering the putative ATPase domain of ABCD4 affect its function, suggesting that the ATPase activity of ABCD4 may be involved in intracellular processing of vitamin B-12.
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