Molecular cloning of Ian4:: a BCR/ABL-induced gene that encodes an outer membrane mitochondrial protein with GTP-binding activity

被引:42
作者
Dahéron, L [1 ]
Zenz, T [1 ]
Siracusa, LD [1 ]
Brenner, C [1 ]
Calabretta, B [1 ]
机构
[1] Thomas Jefferson Univ, Dept Microbiol & Immunol, Kimmel Canc Inst, Philadelphia, PA 19107 USA
关键词
D O I
10.1093/nar/29.6.1308
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
Using the representation difference analysis technique, We have identified a novel gene, Ian4, which is preferentially expressed in hematopoietic precursor 32D cells transfected with wild-type versus mutant forms of the Bcr/Abl oncogene, Ian4 expression was undetectable in 32D cells transfected with v-src, oncogenic Ha-ras or v-Abl, Murine Ian4 maps to chromosome 6, 25 cM from the centromere, The Ian4 mRNA-contains two open reading frames (ORFs) separated by 5 nt, The first ORF has the potential to encode for a polypeptide of 67 amino acids without apparent homology to known proteins. The second ORF encodes a protein of 301 amino acids with a GTP/ATB-binding site in the N-terminus and a hydrophobic domain in the extreme C-terminus, The IAN-4 protein resides in the mitochondrial outer membrane and the last 20 amino acids are necessary for this localization, The IAN-4 protein has GTP-binding activity and shares sequence homology with a novel family of putative GTP-binding proteins: the immuno-associated -nucleotide (IAN) family.
引用
收藏
页码:1308 / 1316
页数:9
相关论文
共 29 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
Argeson AC, 1996, GENETICS, V142, P557
[3]   PHOSPHOLIPASE-C GAMMA-2 (PLCG2) AND PHOSPHOLIPASE-C GAMMA-1 (PLCG1) MAP TO DISTINCT REGIONS IN THE HUMAN AND MOUSE GENOMES [J].
ARGESON, AC ;
DRUCK, T ;
VERONESE, ML ;
KNOPF, JL ;
BUCHBERG, AM ;
HUEBNER, K ;
SIRACUSA, LD .
GENOMICS, 1995, 25 (01) :29-35
[4]   THE CHRONIC MYELOGENOUS LEUKEMIA SPECIFIC P210-PROTEIN IS THE PRODUCT OF THE BCR/ABL HYBRID GENE [J].
BEN-NERIAH, Y ;
DALEY, GQ ;
MESMASSON, AM ;
WITTE, ON ;
BALTIMORE, D .
SCIENCE, 1986, 233 (4760) :212-214
[5]   Translational pathophysiology: a novel molecular mechanism of human disease [J].
Cazzola, M ;
Skoda, RC .
BLOOD, 2000, 95 (11) :3280-3288
[6]   Translational control by an upstream open reading frame in the HER-2/neu transcript [J].
Child, SJ ;
Miller, MK ;
Geballe, AP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (34) :24335-24341
[7]   EXPRESSION OF A DISTINCTIVE BCR-ABL ONCOGENE IN PH1-POSITIVE ACUTE LYMPHOCYTIC-LEUKEMIA (ALL) [J].
CLARK, SS ;
MCLAUGHLIN, J ;
TIMMONS, M ;
PENDERGAST, AM ;
BEN-NERIAH, Y ;
DOW, LW ;
CRIST, W ;
ROVERA, G ;
SMITH, SD ;
WITTE, ON .
SCIENCE, 1988, 239 (4841) :775-777
[8]  
Cortez D, 1996, ONCOGENE, V13, P2589
[9]  
CORTEZ D, 1995, MOL CELL BIOL, V15, P5531
[10]   TRANSFORMATION OF AN INTERLEUKIN-3-DEPENDENT HEMATOPOIETIC-CELL LINE BY THE CHRONIC MYELOGENOUS LEUKEMIA-SPECIFIC P210BER/ABL PROTEIN [J].
DALEY, GQ ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9312-9316