Identification and characterization of a retinoic acid-regulated human homologue of the unc-33-like phosphoprotein gene (hUlip) from neuroblastoma cells

被引:63
作者
Gaetano, C [1 ]
Matsuo, T [1 ]
Thiele, CJ [1 ]
机构
[1] NCI,CELL & MOL BIOL SECT,PEDIAT ONCOL BRANCH,NIH,BETHESDA,MD 20892
关键词
D O I
10.1074/jbc.272.18.12195
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
A cDNA, 7G1, was isolated from retinoic acid (RA) differentiated neuroblastoma cells whose expression was high in human fetal brain and spinal cord mRNA but undetectable in adult brain or non-neuronal tissues. Sequence analysis indicates that 7G1 is homologous to the Caenorhabditis elegans gene unc-33. A 5.5-kilobase pair full-length cDNA from a human fetal brain cDNA library contains an 1710-base pair open reading frame. Because the predicted 570 amino acid sequence of 7G1 shares 98% identity with the murine Ulip gene product, an unc-33-like-phosphoprotein, we refer to 7G1 as the human Ulip (hUlip). hUlip is also similar to the bacterial enzyme D-hydantoinase and the recently described vertebrate gene products CRMP62, TOAD-64, CRMP1, CRMP2, and mUNC. RA stimulates an increase in hUlip mRNA that is transcriptionally regulated. RA stimulates an increase in polypeptides of 58, 60, 65, and 70 kDa with the 58- and 65-kDa species being dephosphorylated forms of the 60- and 70-kDa species. This study presents a model in which to study the regulation and expression of the hUlip gene, a member of an emerging family of molecules that potentially mediates signals involved in axonal outgrowth.
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页码:12195 / 12201
页数:7
相关论文
共 32 条
[1]   RAPID CDNA SEQUENCING (EXPRESSED SEQUENCE TAGS) FROM A DIRECTIONALLY CLONED HUMAN INFANT BRAIN CDNA LIBRARY [J].
ADAMS, MD ;
SOARES, MB ;
KERLAVAGE, AR ;
FIELDS, C ;
VENTER, JC .
NATURE GENETICS, 1993, 4 (04) :373-386
[2]  
BIEDLER JL, 1973, CANCER RES, V33, P2643
[3]  
BRODEUR GM, 1977, CANCER, V40, P2257
[4]  
Byk T, 1996, J NEUROSCI, V16, P688
[5]  
CICCARONE V, 1989, CANCER RES, V49, P219
[6]  
COHEN PS, 1994, BLOOD, V84, P3465
[7]  
COHEN PS, 1995, CANCER RES, V55, P2380
[8]  
CORNAGLIA FP, 1992, CANC LETT, P215
[9]  
FOX F, 1959, CANCER, V12, P108, DOI 10.1002/1097-0142(195901/02)12:1<108::AID-CNCR2820120116>3.0.CO
[10]  
2-H