Identification of Zfp-57 as a downstream molecule of STAT3 and Oct-3/4 in embryonic stem cells

被引:34
作者
Akagi, T
Usuda, M
Matsuda, T
Ko, MSH
Niwa, H
Asano, M
Koide, H
Yokota, T
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Stem Cell Biol, Kanazawa, Ishikawa 9208640, Japan
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
[4] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Kobe, Hyogo 6500047, Japan
[5] Kanazawa Univ, Adv Res Ctr, Inst Expt Anim, Kanazawa, Ishikawa 9208640, Japan
关键词
ES cells; STAT3; Oct-3/4; Zfp-57; self-renewal; targeted disruption; RNAi;
D O I
10.1016/j.bbrc.2005.03.118
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
Embryonic stem (ES) cells are pluripotent cells derived from the inner cell mass of blastocysts. Transcription factor STAT3 is essential for the self-renewal of ES cells. In this study, we searched for downstream molecules of STAT3 in ES cells. Using DNA chip analysis, we obtained zinc finger protein (Zfp)-57. The expression of Zfp-57 was restricted to undifferentiated ES cells and activation of STAT3 led to expression of Zfp-57. We also found that forced expression of a dominant-negative mutant of STAT3 or repression of Oct-3/4 expression led to down-regulation of Zfp-57. Targeted disruption of Zfp-57 resulted in no gross phenotypical defects, including expression of undifferentiated-state-specific genes. These data suggest that Zfp-57 is a downstream molecule of STAT3 and Oct-3/4 in ES cells, although dispensable for their self-renewal. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
相关论文
共 29 条
[21]  
NIWA H, 1991, GENE, V108, P193, DOI 10.1016/0378-1119(91)90434-D
[22]   A NOVEL OCTAMER BINDING TRANSCRIPTION FACTOR IS DIFFERENTIALLY EXPRESSED IN MOUSE EMBRYONIC-CELLS [J].
OKAMOTO, K ;
OKAZAWA, H ;
OKUDA, A ;
SAKAI, M ;
MURAMATSU, M ;
HAMADA, H .
CELL, 1990, 60 (03) :461-472
[23]  
OKAZAKI S, 1994, J BIOL CHEM, V269, P6900
[24]  
Sambrook J, 1989, MOL CLONING LAB MANU
[25]   OCT-4 - A GERMLINE-SPECIFIC TRANSCRIPTION FACTOR MAPPING TO THE MOUSE T-COMPLEX [J].
SCHOLER, HR ;
DRESSLER, GR ;
BALLING, R ;
ROHDEWOHLD, H ;
GRUSS, P .
EMBO JOURNAL, 1990, 9 (07) :2185-2195
[26]   INHIBITION OF PLURIPOTENTIAL EMBRYONIC STEM-CELL DIFFERENTIATION BY PURIFIED POLYPEPTIDES [J].
SMITH, AG ;
HEATH, JK ;
DONALDSON, DD ;
WONG, GG ;
MOREAU, J ;
STAHL, M ;
ROGERS, D .
NATURE, 1988, 336 (6200) :688-690
[27]   Gene expression profiling of embryo-derived stem cells reveals candidate genes associated with pluripotency and lineage specificity [J].
Tanaka, TS ;
Kunath, T ;
Kimber, WL ;
Jaradat, SA ;
Stagg, CA ;
Usuda, M ;
Yokota, T ;
Niwa, H ;
Rossant, J ;
Ko, MSH .
GENOME RESEARCH, 2002, 12 (12) :1921-1928
[28]   MYELOID-LEUKEMIA INHIBITORY FACTOR MAINTAINS THE DEVELOPMENTAL POTENTIAL OF EMBRYONIC STEM-CELLS [J].
WILLIAMS, RL ;
HILTON, DJ ;
PEASE, S ;
WILLSON, TA ;
STEWART, CL ;
GEARING, DP ;
WAGNER, EF ;
METCALF, D ;
NICOLA, NA ;
GOUGH, NM .
NATURE, 1988, 336 (6200) :684-687
[29]   Involvement of Ras in extraembryonic endoderm differentiation of embryonic stem cells [J].
Yoshida-Koide, U ;
Matsuda, T ;
Saikawa, K ;
Nakanuma, Y ;
Yokota, T ;
Asashima, M ;
Koide, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 313 (03) :475-481