Rumi is a CAP10 domain glycosyltransferase that modifies notch and is required for notch signaling

被引:233
作者
Acar, Melih [1 ,2 ]
Jafar-Nejad, Hamed [2 ]
Takeuchi, Hideyuki [4 ]
Rajan, Akhila [2 ]
Ibrani, Dafina [2 ]
Rana, Nadia A. [4 ]
Pan, Hongling [3 ]
Haltiwanger, Robert S. [4 ]
Bellen, Hugo J. [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Howard Hughes Med Inst, Houston, TX 77030 USA
[4] SUNY Stony Brook, Inst Cell & Dev Biol, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
关键词
D O I
10.1016/j.cell.2007.12.016
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
Notch signaling is broadly used to regulate cell-fate decisions. We have identified a gene, rumi, with a temperature-sensitive Notch phenotype. At 28 degrees C-30 degrees C, rumi clones exhibit a full-blown loss of Notch signaling in all tissues tested. However, at 18 degrees C only a mild Notch phenotype is evident. In vivo analyses reveal that the target of Rumi is the extracellular domain of Notch. Notch accumulates intracellularly and at the cell membrane of rumi cells but fails to be properly cleaved, despite normal binding to Delta. Rumi is an endoplasmic reticulum-retained protein with a highly conserved CAP10 domain. Our studies show that Rumi is a protein O-glucosyltransferase, capable of adding glucose to serine residues in Notch EGF repeats with the consensus C-1-X-S-X-P-C-2 sequence. These data indicate that by O-glucosylating Notch in the ER, Rumi regulates its folding and/or trafficking and allows signaling at the cell membrane.
引用
收藏
页码:247 / 258
页数:12
相关论文
共 71 条
[1]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[2]   The BDGP gene disruption project: Single transposon insertions associated with 40% of Drosophila genes [J].
Bellen, HJ ;
Levis, RW ;
Liao, GC ;
He, YC ;
Carlson, JW ;
Tsang, G ;
Evans-Holm, M ;
Hiesinger, PR ;
Schulze, KL ;
Rubin, GM ;
Hoskins, RA ;
Spradling, AC .
GENETICS, 2004, 167 (02) :761-781
[3]   Notch signaling in development and cancer [J].
Bolos, Victoria ;
Grego-Bessa, Joaquin ;
de la Pompa, Jose Luis .
ENDOCRINE REVIEWS, 2007, 28 (03) :339-363
[4]   A novel proteolytic cleavage involved in Notch signaling:: The role of the disintegrin-metalloprotease TACE [J].
Brou, C ;
Logeat, F ;
Gupta, N ;
Bessia, C ;
LeBail, O ;
Doedens, JR ;
Cumano, A ;
Roux, P ;
Black, RA ;
Israël, A .
MOLECULAR CELL, 2000, 5 (02) :207-216
[5]   Glycosyltransferase activity of fringe modulates notch-delta interactions [J].
Brückner, K ;
Perez, L ;
Clausen, H ;
Cohen, S .
NATURE, 2000, 406 (6794) :411-415
[6]   Regulating the Notch pathway in embryonic, adult and old stem cells [J].
Carlson, Morgan E. ;
Conboy, Irina M. .
CURRENT OPINION IN PHARMACOLOGY, 2007, 7 (03) :303-309
[7]   Isolation, characterization, and localization of a capsule-associated gene, CAP10, of Cryptococcus neoformans [J].
Chang, YC ;
Kwon-Chung, KJ .
JOURNAL OF BACTERIOLOGY, 1999, 181 (18) :5636-5643
[8]   Lethal giant discs, a novel C2-domain protein, restricts notch activation during endocytosis [J].
Childress, Jennifer L. ;
Acar, Melih ;
Tao, Chunyao ;
Haider, Georg .
CURRENT BIOLOGY, 2006, 16 (22) :2228-2233
[9]   Aph-1, Pen-2, and nicastrin with presenilin generate an active γ-secretase complex [J].
De Strooper, B .
NEURON, 2003, 38 (01) :9-12
[10]   A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain [J].
De Strooper, B ;
Annaert, W ;
Cupers, P ;
Saftig, P ;
Craessaerts, K ;
Mumm, JS ;
Schroeter, EH ;
Schrijvers, V ;
Wolfe, MS ;
Ray, WJ ;
Goate, A ;
Kopan, R .
NATURE, 1999, 398 (6727) :518-522