Human insulin-like growth factor II leader 2 mediates internal initiation of translation

被引:27
作者
Pedersen, SK
Christiansen, J
Hansen, TVO
Larsen, MR
Nielsen, FC [1 ]
机构
[1] Rigshosp, Dept Clin Biochem, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, RNA Regulat Ctr, Inst Mol Biol, DK-1168 Copenhagen, Denmark
[3] Odense Univ, SDU, Inst Mol Biol & Biochem, Odense, Denmark
关键词
insulin-like growth factors; internal ribosome entry site; translation initiation; 5 ' untranslated region;
D O I
10.1042/0264-6021:3630037
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
Insulin-like growth factor 11 (IGF-II) is a fetal growth factor, which belongs to the family of insulin-like peptides. During fetal life, the IGF-II gene generates three mRNAs with different 5' untranslated regions (UTRs), but identical coding regions and 3' UTRs. We have shown previously that IGF-II leader 3 mRNA translation is regulated by a rapamycin-sensitive pathway, whereas leader 4 mRNA is constitutively translated, but so far the significance of leader 2 mRNA has been unclear. Here, we show that leader 2 mRNA is translated efficiently in an eIF4E-independent manner. In a bicistronic vector system, the 411 nt leader 2 was capable of internal initiation via a phylogenetically conserved internal ribosome entry site (IRES), located in the 3' half of the leader. The IRES is composed of an approx. 120 nt ribosome recruitment element, followed by an 80 nt spacer region, which is scanned by the ribosomal pre-initiation complex. Since cap-dependent translation is down-regulated during cell division, leader 2 might facilitate a continuous IGF-II production in rapidly dividing cells during development.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 35 条
[1]  
Arnaud E, 1999, MOL CELL BIOL, V19, P505
[2]   A 9-nt segment of a cellular mRNA can function as an internal ribosome entry site (IRES) and when present in linked multiple copies greatly enhances IRES activity [J].
Chappell, SA ;
Edelman, GM ;
Mauro, VP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1536-1541
[3]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[4]   Fibroblast growth factor 2 internal ribosome entry site (IRES) activity ex vivo and in transgenic mice reveals a stringent tissue-specific regulation [J].
Créancier, L ;
Morello, D ;
Mercier, P ;
Prats, AC .
JOURNAL OF CELL BIOLOGY, 2000, 150 (01) :275-281
[5]   A GROWTH-DEFICIENCY PHENOTYPE IN HETEROZYGOUS MICE CARRYING AN INSULIN-LIKE GROWTH FACTOR-II GENE DISRUPTED BY TARGETING [J].
DECHIARA, TM ;
EFSTRATIADIS, A ;
ROBERTSON, EJ .
NATURE, 1990, 345 (6270) :78-80
[6]   PARENTAL IMPRINTING OF THE MOUSE INSULIN-LIKE GROWTH FACTOR-II GENE [J].
DECHIARA, TM ;
ROBERTSON, EJ ;
EFSTRATIADIS, A .
CELL, 1991, 64 (04) :849-859
[7]  
DEMOOR CH, 1994, EUR J BIOCHEM, V226, P1039
[8]  
DEMOOR CH, 1994, EUR J BIOCHEM, V222, P1017
[9]  
Ehrenfeld E., 1996, TRANSLATIONAL CONTRO, P549
[10]   Functional characterization of the internal ribosome entry site of eIF4G mRNA [J].
Gan, WN ;
La Celle, M ;
Rhoads, RE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (09) :5006-5012