Globin gene silencing in primary erythroid cultures - An inhibitory role for interleukin-6

被引:29
作者
Ferry, AE
Baliga, SB
Monteiro, C
Pace, BS
机构
[1] UNIV S ALABAMA,DEPT CELLULAR & STRUCT BIOL,MOBILE,AL 36688
[2] UNIV S ALABAMA,DEPT PEDIAT,MOBILE,AL 36688
关键词
D O I
10.1074/jbc.272.32.20030
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
There are numerous similarities between the erythroid and megakaryocytic lineages which suggest that commitment to either lineage occurs relatively late in hematopoiesis. Commitment toward megakaryocyte development requires obligatory silencing of erythroid-specific genes, Therefore, we investigated the effects of interleukin-6, a known inducer of thrombocyte production, on globin gene expression during erythroid differentiation, Studies in K562 cells demonstrated inhibition of gamma globin gene mRNA production and chain biosynthesis in the presence of exogenous interleukin-6 which was abrogated by anti-interleukin-6 monoclonal antibody, Similar studies in primary erythroid progenitors showed inhibition of burst-forming unit-erythroid colony formation when interleukin-6 was added late in cultures with decreased gamma and beta globin gene mRNA production. Protein binding studies demonstrated an increase in activator protein-1 binding to its consensus sequence by 24 h of interleukin-6 treatment, Inhibition of activator protein-1 gene activity had no effect on gamma gene silencing by interleukin-6. A potential interleukin-6 response element was identified in the gamma globin gene, Interleukin-6 treatment led to a rapid increase in protein binding to the target DNA sequence. These results suggest that interleukin-fi may play an important role in globin gene silencing during megakaryocytic lineage commitment.
引用
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页码:20030 / 20037
页数:8
相关论文
共 59 条
[11]  
CARRINGTON PA, 1991, BLOOD, V77, P34
[12]   TRANSCRIPTIONAL REGULATION OF GLOBIN GENE-EXPRESSION IN THE HUMAN ERYTHROID CELL-LINE K562 [J].
CHARNAY, P ;
MANIATIS, T .
SCIENCE, 1983, 220 (4603) :1281-1283
[13]   Cell growth arrest and induction of cyclin-dependent kinase inhibitor p21(WAF1/CIP1) mediated by STAT1 [J].
Chin, YE ;
Kitagawa, M ;
Su, WCS ;
You, ZH ;
Iwamoto, Y ;
Fu, XY .
SCIENCE, 1996, 272 (5262) :719-722
[14]   THE C-FOS PROTEIN INTERACTS WITH C-JUN/AP-1 TO STIMULATE TRANSCRIPTION OF AP-1 RESPONSIVE GENES [J].
CHIU, R ;
BOYLE, WJ ;
MEEK, J ;
SMEAL, T ;
HUNTER, T ;
KARIN, M .
CELL, 1988, 54 (04) :541-552
[15]   DEFINITION OF THE MINIMAL REQUIREMENTS WITHIN THE HUMAN BETA-GLOBIN GENE AND THE DOMINANT CONTROL REGION FOR HIGH-LEVEL EXPRESSION [J].
COLLIS, P ;
ANTONIOU, M ;
GROSVELD, F .
EMBO JOURNAL, 1990, 9 (01) :233-240
[16]  
DAI W, 1993, BLOOD, V81, P1214
[17]   Characterization of a bipotent erythro-megakaryocytic progenitor in human bone marrow [J].
Debili, N ;
Coulombel, L ;
Croisille, L ;
Katz, A ;
Guichard, J ;
BretonGorius, J ;
Vainchenker, W .
BLOOD, 1996, 88 (04) :1284-1296
[18]   MOLECULAR ANALYSIS OF THE HUMAN BETA-GLOBIN LOCUS ACTIVATION REGION [J].
FORRESTER, WC ;
NOVAK, U ;
GELINAS, R ;
GROUDINE, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5439-5443
[19]   INTERFERON BETA-2/B-CELL STIMULATORY FACTOR TYPE-2 SHARES IDENTITY WITH MONOCYTE-DERIVED HEPATOCYTE-STIMULATING FACTOR AND REGULATES THE MAJOR ACUTE PHASE PROTEIN RESPONSE IN LIVER-CELLS [J].
GAULDIE, J ;
RICHARDS, C ;
HARNISH, D ;
LANSDORP, P ;
BAUMANN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (20) :7251-7255
[20]  
GORDON MS, 1993, BLOOD S1, V82, P318