Regulation of Notch signaling by dynamic changes in the precision of S3 cleavage of Notch-1

被引:97
作者
Tagami, Shinji [1 ]
Okochi, Masayasu [1 ]
Yanagida, Kanta [1 ]
Ikuta, Akiko [1 ]
Fukumori, Akio [1 ]
Matsumoto, Naohiko [1 ]
Ishizuka-Katsura, Yoshiko [1 ]
Nakayama, Taisuke [1 ]
Itoh, Naohiro [1 ]
Jiang, Jingwei [1 ]
Nishitomi, Kouhei [1 ]
Kamino, Kouzin [1 ]
Morihara, Takashi [1 ]
Hashimoto, Ryota [1 ]
Tanaka, Toshihisa [1 ]
Kudo, Takashi [1 ]
Chiba, Shigeru [2 ]
Takeda, Masatoshi [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Post Genom & Dis, Div Psychiat & Behav Prote, Suita, Osaka 5650871, Japan
[2] Tokyo Univ Hosp, Dept Cell Therapy & Transplantat Med, Bunkyo Ku, Tokyo 1138655, Japan
关键词
D O I
10.1128/MCB.00863-07
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
Intramembrane proteolysis by presenilin-dependent gamma-secretase produces the Notch intracellular cytoplasmic domain (NCID) and Alzheimer disease-associated amyloid-beta. Here, we show that upon Notch signaling the intracellular domain of Notch-1 is cleaved into two distinct types of NICD species due to diversity in the site of S3 cleavage. Consistent with the N-end rule, the S3-V cleavage produces stable NICD with Val at the N terminus, whereas the S3-S/S3-L cleavage generates unstable NICD with Ser/Leu at the N terminus. Moreover, intracellular Notch signal transmission with unstable NICDs is much weaker than that with stable NICD. Importantly, the extent of endocytosis in target cells affects the relative production ratio of the two types of NICD, which changes in parallel with Notch signaling. Surprisingly, substantial amounts of unstable NICD species are generated from the Val -> Gly and the Lys -> Arg mutants, which have been reported to decrease S3 cleavage efficiency in cultured cells. Thus, we suggest that the existence of two distinct types of NICD points to a novel aspect of the intracellular signaling and that changes in the precision of S3 cleavage play an important role in the process of conversion from extracellular to intracellular Notch signaling.
引用
收藏
页码:165 / 176
页数:12
相关论文
共 52 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]   INVIVO HALF-LIFE OF A PROTEIN IS A FUNCTION OF ITS AMINO-TERMINAL RESIDUE [J].
BACHMAIR, A ;
FINLEY, D ;
VARSHAVSKY, A .
SCIENCE, 1986, 234 (4773) :179-186
[3]   The endocytic protein α-adaptin is required for numb-mediated asymmetric cell division in Drosophila [J].
Berdnik, D ;
Török, T ;
González-Gaitán, M ;
Knoblich, JA .
DEVELOPMENTAL CELL, 2002, 3 (02) :221-231
[4]   Mutations at the P1′ position of Notch1 decrease intracellular domain stability rather than cleavage by γ-secretase [J].
Blat, Y ;
Meredith, JE ;
Wang, Q ;
Bradley, JD ;
Thompson, LA ;
Olson, RE ;
Stern, AM ;
Seiffert, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 299 (04) :569-573
[5]   A transcriptively active complex of APP with Fe65 and histone acetyltransferase Tip60 [J].
Cao, XW ;
Südhof, TC .
SCIENCE, 2001, 293 (5527) :115-120
[6]   Analysis of transmembrane domain mutants is consistent with sequential cleavage of Notch by γ-secretase [J].
Chandu, D ;
Huppert, SS ;
Kopan, R .
JOURNAL OF NEUROCHEMISTRY, 2006, 96 (01) :228-235
[7]  
DE SB, 1999, NATURE, V398, P518
[8]   COMPLEX CELLULAR AND SUBCELLULAR REGULATION OF NOTCH EXPRESSION DURING EMBRYONIC AND IMAGINAL DEVELOPMENT OF DROSOPHILA - IMPLICATIONS FOR NOTCH FUNCTION [J].
FEHON, RG ;
JOHANSEN, K ;
REBAY, I ;
ARTAVANISTSAKONAS, S .
JOURNAL OF CELL BIOLOGY, 1991, 113 (03) :657-669
[9]   Notch signals control the fate of immature progenitor cells in the intestine [J].
Fre, S ;
Huyghe, M ;
Mourikis, P ;
Robine, S ;
Louvard, D ;
Artavanis-Tsakonas, S .
NATURE, 2005, 435 (7044) :964-968
[10]   Presenilin-dependent γ-secretase on plasma membrane and endosomes is functionally distinct [J].
Fukumori, A ;
Okochi, M ;
Tagami, S ;
Jiang, JW ;
Itoh, N ;
Nakayama, T ;
Yanagida, K ;
Ishizuka-Katsura, Y ;
Morihara, T ;
Kamino, K ;
Tanaka, T ;
Kudo, T ;
Tanii, H ;
Ikuta, A ;
Haass, C ;
Takeda, M .
BIOCHEMISTRY, 2006, 45 (15) :4907-4914