Expression of neuronal traits in pancreatic beta cells - Implication of neuron-restrictive silencing factor/repressor element silencing transcription factor, a neuron-restrictive silencer

被引:155
作者
Atouf, F [1 ]
Czernichow, P [1 ]
Scharfmann, R [1 ]
机构
[1] HOP ROBERT DEBRE,INSERM,CJF93 13,F-75019 PARIS,FRANCE
关键词
D O I
10.1074/jbc.272.3.1929
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
Pancreatic beta cells (insulin-producing cells) and neuronal cells share a large number of similarities. Here, we investigate whether the same mechanisms could control the expression of neuronal genes in both neurons and insulin-producing cells. For that purpose, we tested the role of the transcriptional repressor neuron-restrictive silencing factor/repressor element silencing transciption factor (NRSF/REST) in the expression of a battery of neuronal genes in insulin-producing cells. NRSF/REST is a negative regulator of the neuronal fate. It is known to silence neuronal-specific genes in non-neuronal cells. We demonstrate that, as in the case of the neuronal pheochromocytoma cell line PC12, mRNA coding for NRSF/REST is absent from the insulinoma cell line INS-1 and from three other insulin and glucagon producing cell lines. NRSF/REST activity is also absent from insulin-producing cell lines. Transient expression of REST in insulin-producing cell lines is sufficient to silence a reporter gene containing a NRSF/REST binding site, demonstrating the role of NRSF/REST in the expression of neuronal markers in insulin-producing cells. Finally, by searching for the expression of NRSF/REST-regulated genes in insulin-producing cells, we increased the list of the genes expressed in both neurons and insulin-producing cells.
引用
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页码:1929 / 1934
页数:6
相关论文
共 43 条
[1]   HYBRID INSULIN GENES REVEAL A DEVELOPMENTAL LINEAGE FOR PANCREATIC ENDOCRINE-CELLS AND IMPLY A RELATIONSHIP WITH NEURONS [J].
ALPERT, S ;
HANAHAN, D ;
TEITELMAN, G .
CELL, 1988, 53 (02) :295-308
[2]   A RAPID MICROPREPARATION TECHNIQUE FOR EXTRACTION OF DNA-BINDING PROTEINS FROM LIMITING NUMBERS OF MAMMALIAN-CELLS [J].
ANDREWS, NC ;
FALLER, DV .
NUCLEIC ACIDS RESEARCH, 1991, 19 (09) :2499-2499
[3]   EXPRESSION AND REGULATION OF GROWTH-HORMONE (GH) AND PROLACTIN (PRL) RECEPTORS IN A RAT INSULIN-PRODUCING CELL-LINE (INS-1) [J].
ASFARI, M ;
DE, W ;
POSTELVINAY, MC ;
CZERNICHOW, P .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1995, 107 (02) :209-214
[4]   ESTABLISHMENT OF 2-MERCAPTOETHANOL-DEPENDENT DIFFERENTIATED INSULIN-SECRETING CELL-LINES [J].
ASFARI, M ;
JANJIC, D ;
MEDA, P ;
LI, GD ;
HALBAN, PA ;
WOLLHEIM, CB .
ENDOCRINOLOGY, 1992, 130 (01) :167-178
[5]   Dexamethasone regulates the expression of neuronal properties of a rat insulinoma cell line [J].
Atouf, F ;
Tazi, A ;
Polak, M ;
Czernichow, P ;
Scharfmann, R .
JOURNAL OF NEUROENDOCRINOLOGY, 1995, 7 (12) :957-964
[6]   IDENTIFICATION OF THE 64K AUTOANTIGEN IN INSULIN-DEPENDENT DIABETES AS THE GABA-SYNTHESIZING ENZYME GLUTAMIC-ACID DECARBOXYLASE [J].
BAEKKESKOV, S ;
AANSTOOT, HJ ;
CHRISTGAU, S ;
REETZ, A ;
SOLIMENA, M ;
CASCALHO, M ;
FOLLI, F ;
RICHTEROLESEN, H ;
CAMILLI, PD .
NATURE, 1990, 347 (6289) :151-156
[7]  
CASTANO L, 1990, ANNU REV IMMUNOL, V8, P647, DOI 10.1146/annurev.iy.08.040190.003243
[8]   REST - A MAMMALIAN SILENCER PROTEIN THAT RESTRICTS SODIUM-CHANNEL GENE-EXPRESSION TO NEURONS [J].
CHONG, JHA ;
TAPIARAMIREZ, J ;
KIM, S ;
TOLEDOARAL, JJ ;
ZHENG, YC ;
BOUTROS, MC ;
ALTSHULLER, YM ;
FROHMAN, MA ;
KRANER, SD ;
MANDEL, G .
CELL, 1995, 80 (06) :949-957
[9]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[10]   PATHWAYS TO REGULATED EXOCYTOSIS IN NEURONS [J].
DECAMILLI, P ;
JAHN, R .
ANNUAL REVIEW OF PHYSIOLOGY, 1990, 52 :625-645