The inositol polyphosphate 5-phosphatase Ocrl associates with endosomes that are partially coated with clathrin.

Abstract:

:The subcellular localization of Ocrl, the inositol polyphosphate 5-phosphatase that is mutated in Lowe syndrome, was investigated by fluorescence microscopy. Ocrl was localized to endosomes and Golgi membranes along with clathrin, giantin, the mannose 6-phosphate receptor, transferrin, and the early endosomal antigen 1 endosomal marker in fixed cells. The endosomal localization of Ocrl was confirmed by live-cell time-lapse microscopy in which we monitored the dynamics of Ocrl on endosomes. GST binding assays show that Ocrl interacts with the clathrin terminal domain and the clathrin adaptor protein AP-2. Our findings suggest a role for Ocrl in endosomal receptor trafficking and sorting.

authors

Ungewickell A,Ward ME,Ungewickell E,Majerus PW

doi

10.1073/pnas.0405664101

keywords:

subject

Has Abstract

pub_date

2004-09-14 00:00:00

pages

13501-6

issue

37

eissn

0027-8424

issn

1091-6490

pii

0405664101

journal_volume

101

pub_type

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