Mouse TonEBP-NFAT5: expression in early development and alternative splicing

被引:59
作者
Maouyo, D [1 ]
Kim, JY [1 ]
Lee, SD [1 ]
Wu, YH [1 ]
Woo, SK [1 ]
Kwon, HM [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Nephrol, Baltimore, MD 21205 USA
关键词
organic/compatible osmolytes; hypertonicity; transcription factor; tonicity-responsive enhancer binding protein; nuclear factor of activated T cell family;
D O I
10.1152/ajprenal.00123.2001
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Tonicity-responsive enhancer binding protein (TonEBP)-nuclear factor of activated T cell family 5 is a DNA binding protein that plays a key role in the response of cells to hypertonicity. However, TonEBP is expressed and active in tissues that are in an isotonic milieu. To explore the biological role of TonEBP, we cloned mouse TonEBP that shares 92% of amino acids with the human counterpart. TonEBP is expressed in embryonic stem cells and throughout the stages of fetal development. Immunohistochemical analysis shows expression of TonEBP in most, if not all, developing tissues, including the brain, colon, heart, muscle, and eyes. Widespread alternative splicing in exons 2-4 was detected throughout development and in different adult tissues. As a result, four different polypeptides are produced with different lengths at the NH2 terminus. Two of the isoforms differ in their ability to stimulate transcription. In conclusion, the presence of TonEBP mRNA during mouse embryogenesis suggests that TonEBP functions at all stages of mouse development, as well as in isotonic adult tissues.
引用
收藏
页码:F802 / F809
页数:8
相关论文
共 19 条
[1]   Cellular response to osmotic stress in the renal medulla [J].
Beck, FX ;
Burger-Kentischer, A ;
Müller, E .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1998, 436 (06) :814-827
[2]   Hypertonicity-induced phosphorylation and nuclear localization of the transcription factor TonEBP [J].
Dahl, SC ;
Handler, JS ;
Kwon, HM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (02) :C248-C253
[3]   Quantitative PCR analysis of different splice forms of NFAT5 revealed specific gene expression in fetal and adult brain [J].
Dalski, A ;
Wagner, HJ ;
Schwinger, E ;
Zühlke, C .
MOLECULAR BRAIN RESEARCH, 2000, 83 (1-2) :125-127
[4]   Genomic organization of the human NFAT5 gene:: exon-intron structure of the 14-kb transcript and CpG-island analysis of the promoter region [J].
Dalski, A ;
Schwinger, E ;
Zühlke, C .
CYTOGENETICS AND CELL GENETICS, 2001, 93 (3-4) :239-241
[5]   Protection of renal inner medullary epithelial cells from apoptosis by hypertonic stress-induced p53 activation [J].
Dmitrieva, N ;
Kültz, D ;
Michea, L ;
Ferraris, J ;
Burg, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) :18243-18247
[6]   Developmental regulation of Na+/myo-inositol cotransporter gene expression [J].
Guo, W ;
Shimada, S ;
Tajiri, H ;
Yamauchi, A ;
Yamashita, T ;
Okada, S ;
Tohyama, M .
MOLECULAR BRAIN RESEARCH, 1997, 51 (1-2) :91-96
[7]   Cell and molecular biology of organic osmolyte accumulation in hypertonic renal cells [J].
Handler, JS ;
Kwon, HM .
NEPHRON, 2001, 87 (02) :106-110
[8]  
Huang AM, 2000, GENETICS, V156, P1219
[9]   Purification, identification, and characterization of an osmotic response element binding protein [J].
Ko, BCB ;
Turck, CW ;
Lee, KWY ;
Yang, YQ ;
Chung, SSM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 270 (01) :52-61
[10]   Hyperosmolality in the form of elevated NaCl but not urea causes DNA damage in murine kidney cells [J].
Kültz, D ;
Chakravarty, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) :1999-2004