ENO1 gene product binds to the c-myc promoter and acts as a transcriptional repressor:: relationship with Myc promoter-binding protein 1 (MBP-1)

被引:237
作者
Feo, S
Arcuri, D
Piddini, E
Passantino, R
Giallongo, A
机构
[1] Univ Palermo, Dipartimento Biol Cellulare & Sviluppo, I-90128 Palermo, Italy
[2] Ctr Oncobiol Sperimentale, I-90128 Palermo, Italy
[3] CNR, Ist Biol Sviluppo, I-90146 Palermo, Italy
来源
FEBS LETTERS | 2000年 / 473卷 / 01期
关键词
enolase; DNA binding; transcriptional repression; alternative translation;
D O I
10.1016/S0014-5793(00)01494-0
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 Myc promoter-binding protein-1 (MBP-1) is a 37-38 kDa protein that binds to the c-myc P2 promoter and negatively regulates transcription of the protooncogene, MBP-I cDNA shares 97% similarity with the cDNA encoding the glycolytic enzyme alpha-enolase and both genes have been mapped to the same region of human chromosome 1, suggesting the hypothesis that the two proteins might he encoded by the same gene. We shove here data indicating that a 37 kDa protein is alternatively translated from the full-length alpha-enolase mRNA, This shorter form of alpha-enolase is able to bind the MBP-1 consensus sequence and to downregulate expression of a luciferase reporter gene under the control of the c-myc P2 promoter. Furthermore, using alpha-enolase/green fluorescent protein chimeras in transfection experiments we show that, while the 48 kDa alpha-enolase mainly has a cytoplasmic localization, the 37 kDa alpha-enolase is preferentially localized in the cell nuclei, The finding that a transcriptional repressor of the c-myc oncogene is an alternatively translated product of the ENO1 gene, which maps to a region of human chromosome I frequently deleted in human cancers, makes ENO1 a potential candidate for tumor suppressor. (C) 2000 Federation of European Biochemical Societies.
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页码:47 / 52
页数:6
相关论文
共 43 条
[11]  
Ghosh AK, 1999, MOL CELL BIOL, V19, P2880
[12]   STRUCTURAL FEATURES OF THE HUMAN GENE FOR MUSCLE-SPECIFIC ENOLASE - DIFFERENTIAL SPLICING IN THE 5'-UNTRANSLATED SEQUENCE GENERATES 2 FORMS OF MESSENGER-RNA [J].
GIALLONGO, A ;
VENTURELLA, S ;
OLIVA, D ;
BARBIERI, G ;
RUBINO, P ;
FEO, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 214 (02) :367-374
[13]   MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE OF A FULL-LENGTH CDNA FOR HUMAN ALPHA-ENOLASE [J].
GIALLONGO, A ;
FEO, S ;
MOORE, R ;
CROCE, CM ;
SHOWE, LC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (18) :6741-6745
[14]   STRUCTURE OF THE HUMAN GENE FOR ALPHA-ENOLASE [J].
GIALLONGO, A ;
OLIVA, D ;
CALI, L ;
BARBA, G ;
BARBIERI, G ;
FEO, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 190 (03) :567-573
[15]   YEAST HEAT-SHOCK PROTEIN OF MR 48,000 IS AN ISOPROTEIN OF ENOLASE [J].
IIDA, H ;
YAHARA, I .
NATURE, 1985, 315 (6021) :688-690
[16]   Transcriptional repression from the c-myc P2 promoter by the zinc finger protein ZF87/MAZ [J].
Izzo, MW ;
Strachan, GD ;
Stubbs, MC ;
Hall, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :19498-19506
[17]   ENOLASE IS PRESENT AT THE CENTROSOME OF HELA-CELLS [J].
JOHNSTONE, SA ;
WAISMAN, DM ;
RATTNER, JB .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (02) :458-463
[18]  
KNULL HR, 1992, CURR TOP CELL REGUL, V33, P15
[19]   Initiation of translation in prokaryotes and eukaryotes [J].
Kozak, M .
GENE, 1999, 234 (02) :187-208
[20]   A common RNA structural motif involved in the internal initiation of translation of cellular mRNAs [J].
Le, SY ;
Maizel, JV .
NUCLEIC ACIDS RESEARCH, 1997, 25 (02) :362-369