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Molecular cloning of Fyn-associated molecules in the mouse central nervous system
1Laboratory of Neurobiology and Behavioral Genetics, National Institute for Physiological Sciences, Myodaiji, Okazaki, Japan. yagi@nips.ac.jp
Abstract:
Fyn tyrosine kinase is expressed extensively in the central nervous system (CNS) of mammals, and its genetic disruption in mouse displays several behavioral abnormalities with morphological and electrophysiological defects in the brain. To understand the signaling pathways in which Fyn is involved in the CNS, we screened molecules that directly associate with Fyn in neonatal mouse brain by using a two-hybrid yeast system. We isolated five cDNA clones with strong and reproducible Fyn-binding activity. Sequence analyses revealed that three of them are previously reported molecules, SON, tctex-1, and hnRNP K, and that two clones encode novel sequences. The hnRNP K has been shown to associate with Fyn, so our yeast system is appropriate to isolate Fyn-binding molecules. Northern hybridization analyses indicated that all isolated clones are expressed in the mouse brain and that the mRNA levels of the two molecules (tctex-1 and clone 82) change during development in the brain. A full-length cDNA of clone 82 was obtained and its deduced amino acid sequence was homologous to the RNA-binding proteins. Isolation of many Fyn-binding molecules suggest that, in the mouse CNS, Fyn mediates multiple signaling pathways by binding to multiple molecules and that some of these pathways play critical roles in determining a certain type of behavior.
Insights
Fyn tyrosine kinase in the brain binds to multiple molecules, including novel proteins. This interaction suggests Fyn mediates diverse signaling pathways crucial for behavior and brain development.
Area of Science:
- Neuroscience
- Molecular Biology
- Biochemistry
Background:
- Fyn tyrosine kinase is abundant in the mammalian central nervous system (CNS).
- Genetic disruption of Fyn in mice leads to behavioral, morphological, and electrophysiological brain defects.
Purpose of the Study:
- To identify molecules that directly bind to Fyn in the neonatal mouse brain.
- To elucidate the signaling pathways involving Fyn in the CNS.
Main Methods:
- Utilized a two-hybrid yeast system to screen for Fyn-binding molecules.
- Performed sequence analysis, Northern hybridization, and full-length cDNA acquisition for identified clones.
Main Results:
- Isolated five cDNA clones with reproducible Fyn-binding activity, including known proteins (SON, tctex-1, hnRNP K) and two novel sequences.
- Confirmed expression of all isolated clones in the mouse brain.
- Observed developmental changes in mRNA levels for tctex-1 and novel clone 82 in the brain.
Conclusions:
- Fyn interacts with multiple binding partners in the mouse CNS.
- These interactions suggest Fyn's role in mediating diverse signaling pathways.
- Some Fyn-mediated pathways are critical for specific behaviors and brain development.
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