Two Di‐Leucine Motifs Regulate Trafficking of Mucolipin‐1 to Lysosomes

Traffic - Tập 7 Số 3 - Trang 337-353 - 2006
Silvia Vergarajauregui1, Rosa Puertollano1
1Laboratory of Cell Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA

Tóm tắt

Mutations in the mucolipin‐1 gene have been linked to mucolipidosis type IV, a lysosomal storage disorder characterized by severe neurological and ophthalmologic abnormalities. Mucolipin‐1 is a membrane protein containing six putative transmembrane domains with both its N‐ and C‐termini localized facing the cytosol. To gain information on the sorting motifs that mediate the trafficking of this protein to lysosomes, we have generated chimeras in which the N‐ and C‐ terminal tail portions of mucolipin‐1 were fused to a reporter gene. In this article, we report the identification of two separate di‐leucine‐type motifs that co‐operate to regulate the transport of mucolipin‐1 to lysosomes. One di‐leucine motif is positioned at the N‐terminal cytosolic tail and mediates direct transport to lysosomes, whereas the other di‐leucine motif is found at the C‐terminal tail and functions as an adaptor protein 2‐dependent internalization motif. We have also found that the C‐terminal tail of mucolipin‐1 is palmitoylated and that this modification might regulate the efficiency of endocytosis. Finally, the mutagenesis of both di‐leucine motifs abrogated lysosomal accumulation and resulted in cell‐surface redistribution of mucolipin‐1. Taken together, these results reveal novel information regarding the motifs that regulate mucolipin‐1 trafficking and suggest a role for palmitoylation in protein sorting.

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Tài liệu tham khảo

10.1006/mgme.2001.3195

Amir N, 1987, Mucolipidosis type IV: clinical spectrum and natural history, Pediatrics, 79, 953, 10.1542/peds.79.6.953

10.1212/WNL.59.3.306

10.1002/humu.1115

10.1016/0006-291X(75)90526-4

10.1001/archneur.1976.00500120032005

Bach G, 1977, Mucopolysaccarides accumulation in cultured skin fibroblasts derived from patients with Mucolipidosis IV, Am J Hum Genet, 29, 610

10.1002/ajmg.1320120308

10.1097/00005072-199503000-00002

10.1073/pnas.95.11.6373

10.1086/302549

10.1038/79095

10.1016/S0002-9297(07)62941-3

10.1093/hmg/9.17.2471

10.1126/stke.2952005re8

10.1016/S0014-5793(02)03670-0

10.1093/hmg/ddh067

10.1080/0968768031000089546

10.1038/ng0501-64

10.1073/pnas.062065399

10.1073/pnas.0400709101

10.1083/jcb.131.2.351

10.1146/annurev.biochem.72.121801.161800

10.1074/jbc.275.1.261

10.1083/jcb.132.4.577

10.1016/j.febslet.2004.04.080

10.1091/mbc.e05-03-0213

10.1016/0092-8674(89)90685-5

10.1073/pnas.92.22.10207

10.1006/abbi.1996.0047

10.1091/mbc.9.5.1107

Reddy A, 2001, Plasma membrane repair is mediated by Ca(2+) ‐regulated exocytosis of lysosomes, Cell, 106, 157, 10.1016/S0092-8674(01)00421-4

10.1016/S0962-8924(02)00008-9

10.1146/annurev.biochem.73.011303.073954

10.1083/jcb.137.7.1525

10.1083/jcb.148.1.159

10.1074/jbc.M102782200

10.1096/fj.04-3651fje

10.1210/me.2004-0335

10.1091/mbc.01-10-0525

10.1083/jcb.115.6.1573

10.1128/MCB.8.1.466

10.1091/mbc.E02-06-0353