GROWTH AND DIFFERENTIATION OF EMBRYONIC STEM-CELLS THAT LACK AN INTACT C-FOS GENE

被引:59
作者
FIELD, SJ
JOHNSON, RS
MORTENSEN, RM
PAPAIOANNOU, VE
SPIEGELMAN, BM
GREENBERG, ME
机构
[1] HARVARD UNIV, SCH MED, DEPT MICROBIOL & MOLEC GENET, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, DEPT BIOL CHEM & MOLEC PHARMACOL, BOSTON, MA 02115 USA
[3] HARVARD UNIV, SCH MED, DANA FARBER CANC INST, BOSTON, MA 02115 USA
[4] TUFTS UNIV, SCH VET MED, BOSTON, MA 02111 USA
[5] BRIGHAM & WOMENS HOSP, DIV ENDOCRINE, BOSTON, MA 02115 USA
[6] TUFTS UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02111 USA
关键词
D O I
10.1073/pnas.89.19.9306
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The c-fos protooncogene encodes a transcription factor that is thought to play a critical role in proliferation and differentiation as well as in the physiological response of mature cells to their environment. To test directly the role of c-fos in growth and differentiation, we generated mouse embryonic stem cell lines in which both copies of the c-fos gene were specifically disrupted by homologous recombination. Remarkably, the disruption of both copies of c-fos in these cells has no detectable effect on embryonic stem cell viability, growth rate, or differentiation potential. Embryonic stem cells lacking c-fos can differentiate into a wide range of cell types in tissue culture and also in chimeric mice. We conclude that despite a large body of literature suggesting an important role for c-fos in cell growth and differentiation, in at least some cell types this gene is not essential for these processes.
引用
收藏
页码:9306 / 9310
页数:5
相关论文
共 35 条
[1]  
Ausubel FM., 1988, CURRENT PROTOCOLS MO
[2]   TARGETING OF AN INDUCIBLE TOXIC PHENOTYPE IN ANIMAL-CELLS [J].
BORRELLI, E ;
HEYMAN, R ;
HSI, M ;
EVANS, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (20) :7572-7576
[3]  
BRADLEY A, 1987, TERATOCARCINOMAS EMB, P113
[4]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[5]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[6]   FRA-1 - A SERUM-INDUCIBLE, CELLULAR IMMEDIATE-EARLY GENE THAT ENCODES A FOS-RELATED ANTIGEN [J].
COHEN, DR ;
CURRAN, T .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2063-2069
[7]   FOS AND JUN - THE AP-1 CONNECTION [J].
CURRAN, T ;
FRANZA, BR .
CELL, 1988, 55 (03) :395-397
[8]   TRANSCRIPTION FACTOR INTERACTIONS - SELECTORS OF POSITIVE OR NEGATIVE REGULATION FROM A SINGLE DNA ELEMENT [J].
DIAMOND, MI ;
MINER, JN ;
YOSHINAGA, SK ;
YAMAMOTO, KR .
SCIENCE, 1990, 249 (4974) :1266-1272
[9]  
DOETSCHMAN TC, 1985, J EMBRYOL EXP MORPH, V87, P27
[10]   VIRUS INDUCTION OF OSTEOSARCOMAS IN MICE [J].
FINKEL, MP ;
BISKIS, BO ;
JINKINS, PB .
SCIENCE, 1966, 151 (3711) :698-&