SEK-1 MAPKK mediates Ca2+ signaling to determine neuronal asymmetric development in Caenorhabditis elegans

被引:107
作者
Tanaka-Hino, M
Sagasti, A
Hisamoto, N
Kawasaki, M
Nakano, S
Ninomiya-Tsuji, J
Bargmann, CI
Matsumoto, K [1 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Dept Mol Biol, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Japan Sci & Technol Corp, CREST, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[3] Univ Calif San Francisco, Dept Anaerob Microbiol, Program Dev Biol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Anaerob Microbiol, Program Neurosci, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Anaerob Microbiol, Genet Program, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
关键词
D O I
10.1093/embo-reports/kvf001
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 mitogen-activated protein kinase (MAPK) pathway is a highly conserved signaling cascade that converts extracellular signals into various outputs. In Caenorhabditis elegans, asymmetric expression of the candidate odorant receptor STR-2 in either the left or the right of two bilaterally symmetrical olfactory AWC neurons is regulated by axon contact and Ca2+ signaling. We show that the MAPK kinase (MAPKK) SEK-1 is required for asymmetric expression in AWC neurons. Genetic and biochemical analyses reveal that SEK-1 functions in a pathway downstream of UNC-43 and NSY-1, Ca2+/calmodulin-dependent protein kinase II (CaMKII) and MAPK kinase kinase (MAPKKK), respectively. Thus, the NSY-1-SEK-1-MAPK cascade is activated by Ca2+ signaling through CaMKII and establishes asymmetric cell fate decision during neuronal development.
引用
收藏
页码:56 / 62
页数:7
相关论文
共 24 条
[1]   INDEPENDENT HUMAN MAP KINASE SIGNAL-TRANSDUCTION PATHWAYS DEFINED BY MEK AND MKK ISOFORMS [J].
DERIJARD, B ;
RAINGEAUD, J ;
BARRETT, T ;
WU, IH ;
HAN, JH ;
ULEVITCH, RJ ;
DAVIS, RJ .
SCIENCE, 1995, 267 (5198) :682-685
[2]   Asymmetric p38 activation in zebrafish: Its possible role in symmetric and synchronous cleavage [J].
Fujii, R ;
Yamashita, S ;
Hibi, M ;
Hirano, T .
JOURNAL OF CELL BIOLOGY, 2000, 150 (06) :1335-1347
[3]   A conserved p38 mitogen-activated protein kinase pathway regulates Drosophila immunity gene expression [J].
Han, ZQS ;
Enslen, H ;
Hu, XD ;
Meng, XJ ;
Wu, IH ;
Barrett, T ;
Davis, RJ ;
Ip, YT .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (06) :3527-3539
[4]   Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways [J].
Ichijo, H ;
Nishida, E ;
Irie, K ;
tenDijke, P ;
Saitoh, M ;
Moriguchi, T ;
Takagi, M ;
Matsumoto, K ;
Miyazono, K ;
Gotoh, Y .
SCIENCE, 1997, 275 (5296) :90-94
[5]   Signal transduction by the c-Jun N-terminal kinase (JNK) - from inflammation to development [J].
Ip, YT ;
Davis, RJ .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (02) :205-219
[6]   A Caenorhabditis elegans JNK signal transduction pathway regulates coordinated movement via type-D GABAergic motor neurons [J].
Kawasaki, M ;
Hisamoto, N ;
Iino, Y ;
Yamamoto, M ;
Ninomiya-Tsuji, J ;
Matsumoto, K .
EMBO JOURNAL, 1999, 18 (13) :3604-3615
[7]   Sounding the alarm: Protein kinase cascades activated by stress and inflammation [J].
Kyriakis, JM ;
Avruch, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (40) :24313-24316
[8]   Mutations in the alpha 1 subunit of an L-type voltage-activated Ca2+ channel cause myotonia in Caenorhabditis elegans [J].
Lee, RYN ;
Lobel, L ;
Hengartner, M ;
Horvitz, HR ;
Avery, L .
EMBO JOURNAL, 1997, 16 (20) :6066-6076
[9]   EFFICIENT GENE-TRANSFER IN C-ELEGANS - EXTRACHROMOSOMAL MAINTENANCE AND INTEGRATION OF TRANSFORMING SEQUENCES [J].
MELLO, CC ;
KRAMER, JM ;
STINCHCOMB, D ;
AMBROS, V .
EMBO JOURNAL, 1991, 10 (12) :3959-3970
[10]   Purification and identification of a major activator for p38 from osmotically shocked cells - Activation of mitogen-activated protein kinase 6 by osmotic shock, tumor necrosis factor-alpha, and H2O2 [J].
Moriguchi, T ;
Toyoshima, F ;
Gotoh, Y ;
Iwamatsu, A ;
Irie, K ;
Mori, E ;
Kuroyanagi, N ;
Hagiwara, M ;
Matsumoto, K ;
Nishida, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (43) :26981-26988