A cell proliferation-dependent multiprotein complex NC-3A positively regulates the CD34 promoter via a TCATTT-Coutaining element

被引:10
作者
Perrotti, D
Bellon, T
Trotta, R
Martinez, R
Calabretta, B
机构
[1] THOMAS JEFFERSON UNIV, JEFFERSON CANC INST, DEPT MICROBIOL & IMMUNOL, PHILADELPHIA, PA 19107 USA
[2] THOMAS JEFFERSON UNIV, JEFFERSON CANC INST, KIMMEL CANC INST, PHILADELPHIA, PA 19107 USA
关键词
D O I
10.1182/blood.V88.9.3336.bloodjournal8893336
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The CD34 cell surface antigen is a glycoprotein expressed by hematopoietic stem and progenitor cells and also by certain nonhematopoietic cell types. Because CD34 expression is regulated both at the transcriptional and the posttranscriptional level, we attempted to identify factors that, by interacting with the 5' flanking region of the human CD34 gene, may regulate its promoter activity in proliferating hematopoietic cells. By electrophoretic mobility shift assay, UV cross-linking and DNase I footprinting analyses, we identified a multiprotein complex, designated NC-3A, that specifically interacts with the CD34 promoter region from nucleotides -375 to -351. Sequence analysis of this region revealed the presence of a distinct motif, TCATTT. Chloramphenicol acetyl-transferase assays used to assess promoter activity in transiently transfected cells showed that this TCATTT-containing element, which is conserved in both the human and the murine CD34 genes, mediates positive regulatory activity in hematopoietic and nonhematopoietic cells, and acts as an enhancer when placed upstream of a heterologous promoter. Moreover, loss of CD34 promoter activity was caused by mutation of the TCATTT motif. In addition, the interaction of the nuclear multiprotein complex NC-3A with this enhancer element is prolife ration-dependent. These data indicate that, although not cell-type specific, the formation of a multiprotein complex NC-OA interacting with the region from nucleotides -375 to -351 plays an important role in controlling CD34 promoter activity in proliferating hematopoietic cells. (C) 1996 by The American Society of Hematology.
引用
收藏
页码:3336 / 3348
页数:13
相关论文
共 45 条
[1]   BINDING OF L-SELECTIN TO THE VASCULAR SIALOMUCIN CD34 [J].
BAUMHUETER, S ;
SINGER, MS ;
HENZEL, W ;
HEMMERICH, S ;
RENZ, M ;
ROSEN, SD ;
LASKY, LA .
SCIENCE, 1993, 262 (5132) :436-438
[2]   ANTIGEN CD34+ MARROW-CELLS ENGRAFT LETHALLY IRRADIATED BABOONS [J].
BERENSON, RJ ;
ANDREWS, RG ;
BENSINGER, WI ;
KALAMASZ, D ;
KNITTER, G ;
BUCKNER, CD ;
BERNSTEIN, ID .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (03) :951-955
[3]  
BERENSON RJ, 1991, BLOOD, V77, P1717
[4]   LOCALIZATION OF THE INDUCIBLE ENHANCER IN THE MOUSE INTERLEUKIN-5 GENE THAT IS RESPONSIVE TO T-CELL RECEPTOR STIMULATION [J].
BOURKE, PF ;
VANLEEUWEN, BH ;
CAMPBELL, HD ;
YOUNG, IG .
BLOOD, 1995, 85 (08) :2069-2077
[5]   THE GENE ENCODING THE STEM-CELL ANTIGEN, CD34, IS CONSERVED IN MOUSE AND EXPRESSED IN HEMATOPOIETIC PROGENITOR-CELL LINES, BRAIN, AND EMBRYONIC FIBROBLASTS [J].
BROWN, J ;
GREAVES, MF ;
MOLGAARD, HV .
INTERNATIONAL IMMUNOLOGY, 1991, 3 (02) :175-184
[6]  
BURN TC, 1992, BLOOD, V80, P3051
[7]  
CHAN SH, 1992, J IMMUNOL, V148, P92
[8]   Hematopoietic defects in mice lacking the sialomucin CD34 [J].
Cheng, J ;
Baumhueter, S ;
Cacalano, G ;
CarverMoore, K ;
Thibodeaux, H ;
Thomas, R ;
Broxmeyer, HE ;
Cooper, S ;
Hague, N ;
Moore, M ;
Lasky, LA .
BLOOD, 1996, 87 (02) :479-490
[9]   ISOLATION OF TRANSCRIPTION FACTORS THAT DISCRIMINATE BETWEEN DIFFERENT PROMOTERS RECOGNIZED BY RNA POLYMERASE-II [J].
DYNAN, WS ;
TJIAN, R .
CELL, 1983, 32 (03) :669-680
[10]  
FACKLER MJ, 1990, J BIOL CHEM, V265, P11056