SARA-regulated vesicular targeting underlies formation of the Light-Sensing organelle in mammalian rods

被引:117
作者
Chuang, Jen-Zen
Zhao, Yu
Sung, Ching-Hwa
机构
[1] Cornell Univ, Weill Med Coll, Dept Ophthalmol, Margaret M Dyson Res Inst, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Cell & Dev Biol, New York, NY 10021 USA
关键词
D O I
10.1016/j.cell.2007.06.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The light-sensing organelle of the vertebrate rod photoreceptor, the outer segment (OS), is a modified cilium containing similar to 1,000 stacked disc membranes that are densely packed with visual pigment rhodopsin. The mammalian OS is renewed every ten days; new discs are assembled at the base of the OS by a poorly understood mechanism. Our results suggest that discs are formed and matured in a process that involves specific phospholipid-directed vesicular membrane targeting. Rhodopsin-laden vesicles in the OS axonemal cytoplasm fuse with nascent discs that are highly specialized with abundant phosphatidylinositol 3-phosphate (PI3P). This membrane coupling is regulated by the FYVE domain-containing protein, SARA, through its direct interaction with PI3P, rhodopsin, and SNARE protein syntaxin 3. Our model, in contrast to the previously proposed evagination model, suggests that the vesicular delivery of rhodopsin in the OS concentrates rhodopsin into discs, and this process directly participates in disc biogenesis.
引用
收藏
页码:535 / 547
页数:13
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