Loss of LKLF function results in embryonic lethality in mice

被引:132
作者
Wani, MA
Means, RT
Lingrel, JB [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[2] Vet Affairs Med Ctr, Cincinnati, OH 45267 USA
关键词
LKLF; gene targeting; embryonic lethality;
D O I
10.1023/A:1008809809843
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Lung Kruppel-like factor (LKLF) is a member of the Kruppel-like family of zinc finger transcription factors and is closely related to erythroid kruppel-like factor (EKLF), which is necessary for P-globin gene expression. While EKLF is expressed exclusively in erythroid cells, LKLF is expressed temporally during early embryonic development and predominantly in the adult mouse lung. To understand the role this novel transcription factor plays in development as well as tissue differentiation and function, animals lacking LKLF were produced using gene targeting technology. Mice lacking LKLF die in utero between day 11.5 and 13.5 of embryonic life and exhibit retarded growth, craniofacial abnormalities, abdominal bleeding and signs of anaemia. Although the yolk sac erythropoiesis is normal in mutant embryos, in vitro fetal liver cultures of these embryos fail to give rise to erythroid cells. Expression of other erythroid specific genes such as EKLF, GATA1 and GATA3 is unaltered in these animals. These findings demonstrate the LKLF function is indispensable during normal embryonic development, and although both LKLF and EKLF recognize common DNA motifs, they do not substitute for each other.
引用
收藏
页码:229 / 238
页数:10
相关论文
共 34 条
[1]  
ANDERSON KP, 1995, MOL CELL BIOL, V15, P5957
[2]   SITE-DIRECTED POINT MUTATIONS IN EMBRYONIC STEM-CELLS - A GENE-TARGETING TAG-AND-EXCHANGE STRATEGY [J].
ASKEW, GR ;
DOETSCHMAN, T ;
LINGREL, JB .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (07) :4115-4124
[3]  
BIEKER JJ, 1995, MOL CELL BIOL, V15, P852
[4]   ISOLATION AND CHARACTERIZATION OF A ZINC FINGER POLYPEPTIDE GENE AT THE HUMAN CHROMOSOME-11 WILMS TUMOR LOCUS [J].
CALL, KM ;
GLASER, T ;
ITO, CY ;
BUCKLER, AJ ;
PELLETIER, J ;
HABER, DA ;
ROSE, EA ;
KRAL, A ;
YEGER, H ;
LEWIS, WH ;
JONES, C ;
HOUSMAN, DE .
CELL, 1990, 60 (03) :509-520
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   A GENE ACTIVATED IN MOUSE 3T3-CELLS BY SERUM GROWTH-FACTORS ENCODES A PROTEIN WITH ZINC FINGER SEQUENCES [J].
CHRISTY, BA ;
LAU, LF ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :7857-7861
[7]  
Crossley M, 1996, MOL CELL BIOL, V16, P1695
[8]   ROLE OF ERYTHROID KRUPPEL-LIKE FACTOR IN HUMAN GAMMA-GLOBIN TO BETA-GLOBIN GENE SWITCHING [J].
DONZE, D ;
TOWNES, TM ;
BIEKER, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (04) :1955-1959
[9]  
FENG WC, 1994, J BIOL CHEM, V269, P1493
[10]   Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1 [J].
Fujiwara, Y ;
Browne, CP ;
Cunniff, K ;
Goff, SC ;
Orkin, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12355-12358