TY - JOUR
T1 - Altered Gene Expression in the Adult Brain of fyn-Deficient Mice
AU - Goto, June
AU - Tezuka, Tohru
AU - Nakazawa, Takanobu
AU - Tsukamoto, Nobuo
AU - Nakamura, Takahisa
AU - Ajima, Rieko
AU - Yokoyama, Kazumasa
AU - Ohta, Tsutomu
AU - Ohki, Misao
AU - Yamamoto, Tadashi
N1 - Funding Information:
We thank Dr J. Imai for his technical help with real-time PCR, and Dr H. Asou for critical discussions. This work was funded in part by a grant-in-aid and the Special Coordination Funds for Promoting Science and Technology from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. This study was also supported by the Program for Promotion of Fundamental Studies in Health Science of the Organization for Pharmaceutical Safety and Research, Japan.
PY - 2004/2
Y1 - 2004/2
N2 - 1. Fyn, a member of Src-family tyrosine kinases is implicated in both brain development and adult brain function. Recent studies have identified some Fyn substrates, however, little is known about the transcriptional targets for Fyn mediated signaling pathways. In the present study, we sought to identify targets downstream of Fyn in vivo. 2. We compared genes expressed in adult hippocampi of wild-type and fyn-deficient mice using gene chips containing more than 12,000 genes. 3. The results showed that 559 transcripts were expressed differentially between these mice. Expression of 20 genes including a substantial number of myelin-associated genes was strongly repressed in fyn-deficient mice. 4. Reduced expression of these myelin-associated genes, such as MBP and MOG, in fyn-deficient mice was also confirmed by real-time PCR and northern blotting, arguing that Fyn is important for function and development of oligodendrocytes. 5. Further analysis of the genes that are differently expressed in fyn-deficient mice may shed light on the molecular mechanism by which Fyn regulates adult neural function.
AB - 1. Fyn, a member of Src-family tyrosine kinases is implicated in both brain development and adult brain function. Recent studies have identified some Fyn substrates, however, little is known about the transcriptional targets for Fyn mediated signaling pathways. In the present study, we sought to identify targets downstream of Fyn in vivo. 2. We compared genes expressed in adult hippocampi of wild-type and fyn-deficient mice using gene chips containing more than 12,000 genes. 3. The results showed that 559 transcripts were expressed differentially between these mice. Expression of 20 genes including a substantial number of myelin-associated genes was strongly repressed in fyn-deficient mice. 4. Reduced expression of these myelin-associated genes, such as MBP and MOG, in fyn-deficient mice was also confirmed by real-time PCR and northern blotting, arguing that Fyn is important for function and development of oligodendrocytes. 5. Further analysis of the genes that are differently expressed in fyn-deficient mice may shed light on the molecular mechanism by which Fyn regulates adult neural function.
KW - Adult brain functions
KW - Gene expression
KW - Myelination
KW - Tyrosine kinase
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U2 - 10.1023/B:CEMN.0000012720.71630.14
DO - 10.1023/B:CEMN.0000012720.71630.14
M3 - Article
C2 - 15049519
AN - SCOPUS:10744233616
SN - 0272-4340
VL - 24
SP - 149
EP - 159
JO - Cellular and Molecular Neurobiology
JF - Cellular and Molecular Neurobiology
IS - 1
ER -