Identification of putative downstream genes of Oct-3, a pluripotent cell-specific transcription factor

被引:53
作者
Saijoh, Y
Fujii, H
Meno, C
Sato, M
Hirota, Y
Nagamatsu, S
Ikeda, M
Hamada, H
机构
[1] TOKYO METROPOLITAN INST MED SCI,BUNKYO KU,TOKYO 113,JAPAN
[2] KYORIN UNIV,FAC MED,DEPT BIOCHEM,MITAKA,TOKYO 181,JAPAN
[3] MBL CO LTD,INA LAB,NAGANO 396,JAPAN
关键词
D O I
10.1046/j.1365-2443.1996.d01-237.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Oct-3, a pluripotent cell-specific POU transcription factor, appears to be a key regulator in pluripotential early embryonic cells and germ cells. In order to study how pluripotency is maintained, it is essential to know what genes are regulated by Oct-3. Results: By employing a subtraction method, we identified several pluripotent cell-specific genes. Based upon expression patterns in various cell lines lacking or possessing Oct-3 function, about half of the genes were placed downstream of Oct-3. These downstream genes included a previously-known gene (Glut-3: a gene for a glucose transporter) and novel genes (226, 383 and 880). Their expression patterns paralleled that of Oct-3: all of these genes were highly expressed in pluripotent cells such as EC/ES cells, but switched off upon differentiation. More importantly, their expression was rescued in 'revertant' cells that ectopically acquired the Oct-3 transactivating function. Furthermore, the expression profiles of Glut-3, 226 and 383 during mouse development also overlapped that of Oct-3. The Glut-3 gene possessed multiple Oct-3 binding sites in its transcriptional regulatory regions, suggesting that at least one of the downstream genes was a direct target of Oct-3. Conclusions: A large proportion of pluripotent cell-specific genes appear to be downstream targets of Oct-3.
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页码:239 / 252
页数:14
相关论文
共 21 条
[1]   AN EMBRYONICALLY EXPRESSED GENE IS A TARGET FOR C-MYC REGULATION VIA THE C-MYC-BINDING SEQUENCE [J].
BENVENISTY, N ;
LEDER, A ;
KUO, A ;
LEDER, P .
GENES & DEVELOPMENT, 1992, 6 (12B) :2513-2523
[2]  
BRULET P, 1983, P NATL ACAD SCI USA, V82, P5641
[3]   AN UNUSUAL ACTIVE HEXOSE-TRANSPORT SYSTEM IN HUMAN AND MOUSE PREIMPLANTATION EMBRYOS [J].
CHI, MMY ;
MANCHESTER, JK ;
BASURAY, R ;
MAHENDRA, S ;
STRICKLER, RC ;
MCDOUGAL, DB ;
LOWRY, OH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (21) :10023-10025
[4]  
EL DW, 1993, CELL, V75, P817
[5]   STRINGENT INTEGRITY REQUIREMENTS FOR BOTH TRANSACTIVATION AND DNA-BINDING IN A TRANSACTIVATOR, OCT3 [J].
IMAGAWA, M ;
MIYAMOTO, A ;
SHIRAKAWA, M ;
HAMADA, H ;
MURAMATSU, M .
NUCLEIC ACIDS RESEARCH, 1991, 19 (16) :4503-4508
[6]  
Kobayashi T, 1994, DNA Res, V1, P15, DOI 10.1093/dnares/1.1.15
[7]   IMMUNOHISTOCHEMICAL LOCALIZATION OF THE NEURON-SPECIFIC GLUCOSE-TRANSPORTER (GLUT3) TO NEUROPIL IN ADULT-RAT BRAIN [J].
MCCALL, AL ;
VANBUEREN, AM ;
MOHOLTSIEBERT, M ;
CHERRY, NJ ;
WOODWARD, WR .
BRAIN RESEARCH, 1994, 659 (1-2) :292-297
[8]  
NAGAMATSU S, 1992, J BIOL CHEM, V267, P467
[9]   CYCLIN-G IS A TRANSCRIPTIONAL TARGET OF THE P53 TUMOR-SUPPRESSOR PROTEIN [J].
OKAMOTO, K ;
BEACH, D .
EMBO JOURNAL, 1994, 13 (20) :4816-4822
[10]   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