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Meis2 is essential for cranial and cardiac neural crest development
Ondrej Machon1, Jan Masek2, Olga Machonova3
1Institute of Molecular Genetics, The Czech Academy of Sciences, 14200, Praha, Czech Republic. machon@img.cas.cz.
BMC Developmental Biology
|November 8, 2015
Summary
Meis2 is essential for mouse development, with its absence causing embryonic lethality and severe defects in neural crest-derived tissues, including the heart and craniofacial structures.
Area of Science:
- Developmental Biology
- Genetics
- Molecular Biology
Background:
- TALE-class homeodomain transcription factors Meis and Pbx are crucial for embryonic development.
- While Pbx and Meis1 functions are known, Meis2's role in mouse embryogenesis remained uncharacterized.
- Systemic Meis2 gene inactivation in mice leads to embryonic lethality by day 14, accompanied by hemorrhaging.
Purpose of the Study:
- To investigate the functional role of Meis2 during mouse embryogenesis.
- To determine the specific developmental processes regulated by Meis2, particularly in neural crest cells.
Main Methods:
- Generation of a conditional Meis2 allele in mice.
- Systemic inactivation of the Meis2 gene.
- Conditional inactivation of Meis2 in neural crest cells using an AP2α-IRES-Cre driver line.
Main Results:
- Meis2 is expressed in neural crest cells.
- Meis2-deficient embryos exhibit defects in neural crest-derived tissues, including abnormal heart outflow tracts (persistent truncus arteriosus) and cranial nerves.
- Conditional inactivation in neural crest cells results in craniofacial skeleton anomalies, heart defects, and cranial nerve abnormalities.
Conclusions:
- Meis2 is essential for mouse embryonic development, with null mutants being embryonic lethal.
- Meis2 plays a critical role in the development of cranial and cardiac neural crest cells in mice.
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