Lung Kruppel-like factor, a zinc finger transcription factor, is essential for normal lung development

被引:105
作者
Wani, MA
Wert, SE
Lingrel, JB
机构
[1] Univ Cincinnati, Coll Med, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[2] Childrens Hosp Med Ctr, Div Pulm Biol, Cincinnati, OH 45267 USA
关键词
D O I
10.1074/jbc.274.30.21180
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
Lung Kruppel-like factor (LKLF) is a member of the Kruppel-like factor family of transcription factors and is highly expressed in lung with limited distribution in other tissues. Mice lacking LKLF due to inactivation of LKLF by gene targeting die in utero at midgestation around day 12.5 due to severe hemorrhage, making it difficult to study the role of this transcription factor in lung development and function, However, in vitro organ culture of lung buds removed from 11.5-day-old LKLF-/- embryos show normal tracheobronchial tree formation. To examine later stages of lung development, the embryonic lethality due to germ line LKLF null mutation was circumvented, by constructing LKLF homozygous null mouse embryonic stem cells, using a two-step gene targeting procedure, and determining whether these cells give rise to lung tissue, The targeted cells were used to produce chimeric animals, and the contribution of LKLF-deficient cells to the formation of various internal organs was analyzed, In chimeric mice that survived after birth, null embryonic stem cells contributed significantly to all of the major organs except the lungs, On the other hand, some highly chimeric animals died at birth, and histopathological examination of their lungs suggested abnormalities in their lung development, These studies show that LKLF plays an important role in normal lung development.
引用
收藏
页码:21180 / 21185
页数:6
相关论文
共 44 条
[1]  
ANDERSON KP, 1995, MOL CELL BIOL, V15, P5957
[2]  
BRADLEY A, 1987, TERATOCARCINOMAS EMB, P112
[3]  
CARDOSO WV, 1995, AM J PHYSIOL, V13, pL492
[4]   Targeted disruption of the ubiquitous CNC-bZIP transcription factor, Nrf-1, results in anemia and embryonic lethality in mice [J].
Chan, JY ;
Kwong, M ;
Lu, RH ;
Chang, J ;
Wang, B ;
Yen, TSB ;
Kan, YW .
EMBO JOURNAL, 1998, 17 (06) :1779-1787
[5]   EMBRYONIC LETHALITY IN MICE HOMOZYGOUS FOR A TARGETED DISRUPTION OF THE N-MYC GENE [J].
CHARRON, J ;
MALYNN, BA ;
FISHER, P ;
STEWART, V ;
JEANNOTTE, L ;
GOFF, SP ;
ROBERTSON, EJ ;
ALT, FW .
GENES & DEVELOPMENT, 1992, 6 (12A) :2248-2257
[6]   PROBING IMMUNE FUNCTIONS IN RAG-DEFICIENT MICE [J].
CHEN, JZ ;
SHINKAI, Y ;
YOUNG, F ;
ALT, FW .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (02) :313-319
[7]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[8]   A gene encoding an intestinal-enriched member of the Kruppel-like factor family expressed in intestinal epithelial cells [J].
Conkright, MD ;
Wani, MA ;
Anderson, KP ;
Lingrel, JB .
NUCLEIC ACIDS RESEARCH, 1999, 27 (05) :1263-1270
[9]  
Crossley M, 1996, MOL CELL BIOL, V16, P1695
[10]   A gene for a novel zinc-finger protein expressed in differentiated epithelial cells and transiently in certain mesenchymal cells [J].
GarrettSinha, LA ;
Eberspaecher, H ;
Seldin, MF ;
deCrombrugghe, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (49) :31384-31390