The cytoplasmic polyadenylation element binding protein and polyadenylation of messenger RNA in Aplysia neurons

被引:39
作者
Liu, JM [1 ]
Schwartz, JH [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY 10032 USA
关键词
nerve terminal; synaptosome; long-term facilitation; memory formation;
D O I
10.1016/S0006-8993(02)03729-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Translation of some mRNAs in nerve terminals has been shown to be regulated by polyadenylation in an experience-dependent manner. The transcripts whose translation is controlled by regulated polyadenylation contain the cytoplasmic polyadenylation element (CPE), which binds to the highly conserved CPE-binding protein (CPEB). In Aplysia, neuron-specific actin mRNA, which has a CPE in its 3' UTR, is located both in cell bodies and at nerve endings (synaptosomes). We found that actin mRNA from pleural ganglion sensory neurons becomes polyadenylated during long-term facilitation produced by treatment with serotonin or 8-bromo cAMP. We cloned two isoforms of CPEB (ApCPEB77 and ApCEPB49) from Aplysia nervous tissue. The larger form, which is predominant in nervous tissue, is similar to p82, the clam binding protein, as well as to vertebrate CPEBs. Moreover, synaptosomal actin mRNAs are polyadenylated following the treatment with 5-HT. Since both CPEB and polyadenylated actin mRNA are present in synaptosomes and synaptosomal actin protein increases during long-term facilitation, we suggest that the translation of actin message in nerve endings is up-regulated by polyadenylation to grow new synapses. (C) 2002 Elsevier Science B.V.. All rights reserved.
引用
收藏
页码:68 / 76
页数:9
相关论文
共 47 条
[1]   C/EBP IS AN IMMEDIATE-EARLY GENE REQUIRED FOR THE CONSOLIDATION OF LONG-TERM FACILITATION IN APLYSIA [J].
ALBERINI, CM ;
GHIRARDI, M ;
METZ, R ;
KANDEL, ER .
CELL, 1994, 76 (06) :1099-1114
[2]   The Aurora/Ipi1p kinase family: regulators of chromosome segregation and cytokinesis [J].
Bischoff, JR ;
Plowman, GD .
TRENDS IN CELL BIOLOGY, 1999, 9 (11) :454-459
[3]   IDENTIFICATION OF A PEPTIDE SPECIFIC FOR APLYSIA SENSORY NEURONS BY PCR-BASED DIFFERENTIAL SCREENING [J].
BRUNET, JF ;
SHAPIRO, E ;
FOSTER, SA ;
KANDEL, ER ;
IINO, Y .
SCIENCE, 1991, 252 (5007) :856-859
[4]   A transient, neuron-wide form of CREB-mediated long-term facilitation can be stabilized at specific synapses by local protein synthesis [J].
Casadio, A ;
Martin, KC ;
Giustetto, M ;
Zhu, HX ;
Chen, M ;
Bartsch, D ;
Bailey, CH ;
Kandel, ER .
CELL, 1999, 99 (02) :221-237
[5]  
CHAIN DG, 1995, J NEUROSCI, V15, P7592
[6]  
CHIN GJ, 1989, J NEUROSCI, V9, P38
[7]   Mechanism and regulation of mRNA polyadenylation [J].
Colgan, DF ;
Manley, JL .
GENES & DEVELOPMENT, 1997, 11 (21) :2755-2766
[8]   Cytoplasmic polyadenylation elements mediate masking and unmasking of cyclin B1 mRNA [J].
de Moor, CH ;
Richter, JD .
EMBO JOURNAL, 1999, 18 (08) :2294-2303
[9]   A NOVEL ACTIN CDNA IS EXPRESSED IN THE NEURONS OF APLYSIA-CALIFORNICA [J].
DESGROSEILLERS, L ;
AUCLAIR, D ;
WICKHAM, L ;
MAALOUF, M .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1994, 1217 (03) :322-324
[10]  
Fumagalli S, 2000, COLD SPRING HARBOR M, V39, P695