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Mouse TonEBP-NFAT5: expression in early development and alternative splicing.
Djikolngar Maouyo1, Jee Y Kim, Sang D Lee
1Division of Nephrology, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.
American Journal of Physiology. Renal Physiology
|April 6, 2002
Summary
Tonicity-responsive enhancer binding protein (TonEBP) is crucial for cellular responses to hypertonicity. This study reveals TonEBP
Area of Science:
- Molecular Biology
- Cell Biology
- Developmental Biology
Background:
- Tonicity-responsive enhancer binding protein (TonEBP), also known as nuclear factor of activated T cells family 5, is a DNA-binding protein.
- TonEBP is recognized for its role in cellular responses to hypertonic stress.
- However, its expression and activity in isotonic environments suggest broader biological functions.
Purpose of the Study:
- To investigate the biological role of TonEBP beyond hypertonic stress.
- To clone and characterize mouse TonEBP and compare it to its human counterpart.
- To examine the expression patterns and alternative splicing of TonEBP during development and in adult tissues.
Main Methods:
- Cloning of mouse TonEBP.
- Immunohistochemical analysis of TonEBP expression in developing tissues.
- Analysis of alternative splicing of TonEBP mRNA in various tissues and developmental stages.
Main Results:
- Mouse TonEBP shares 92% amino acid similarity with human TonEBP.
- TonEBP is expressed in embryonic stem cells and throughout fetal development in multiple tissues, including brain, colon, heart, muscle, and eyes.
- Widespread alternative splicing of TonEBP exons 2-4 generates four distinct N-terminal polypeptides, two of which exhibit differential transcriptional activity.
Conclusions:
- The presence of TonEBP mRNA during mouse embryogenesis indicates its function throughout development.
- TonEBP is likely involved in the biology of isotonic adult tissues.
- Alternative splicing of TonEBP contributes to functional diversity, suggesting roles beyond osmotic regulation.