TY - JOUR
T1 - Interference with activity-dependent transcriptional activation of BDNF gene depending upon the expanded polyglutamines in neurons
AU - Miyashita, Toshihide
AU - Tabuchi, Akiko
AU - Fukuchi, Mamoru
AU - Hara, Daichi
AU - Kisukeda, Tomochika
AU - Shimohata, Takayoshi
AU - Tsuji, Shoji
AU - Tsuda, Masaaki
PY - 2005/8/12
Y1 - 2005/8/12
N2 - Expanded polyglutamines (polyQ) have been demonstrated to impair the CREB-dependent transcription in established cell lines. Since activity-dependent transcription in neurons, which plays an important role in forming neuronal plasticity, is largely controlled by CREB, it is important to study whether polyQ interferes with the activity-dependent transcriptional activation of genes in neurons. In cultured rat cortical neurons, over-expression of truncated dentatorubral-pallidoluysian atrophy proteins containing expanded polyQ, which form aggregation bodies in nucleus, reduced the calcium (Ca2+) signal-mediated transcriptional activation of brain-derived neurotrophic factor, c-fos, and pituitary adenylate cyclase-activating polypeptide gene promoters in a dose-dependent manner. The interference with the transcriptional activation was dependent upon the presence of polyQ, the strength of which was increased as the length of polyQ stretches was expanded. Thus, polyQ interferes with the activity-dependent transcription in a polyQ-length-dependent manner, which may correspond to the severity of polyglutamine diseases.
AB - Expanded polyglutamines (polyQ) have been demonstrated to impair the CREB-dependent transcription in established cell lines. Since activity-dependent transcription in neurons, which plays an important role in forming neuronal plasticity, is largely controlled by CREB, it is important to study whether polyQ interferes with the activity-dependent transcriptional activation of genes in neurons. In cultured rat cortical neurons, over-expression of truncated dentatorubral-pallidoluysian atrophy proteins containing expanded polyQ, which form aggregation bodies in nucleus, reduced the calcium (Ca2+) signal-mediated transcriptional activation of brain-derived neurotrophic factor, c-fos, and pituitary adenylate cyclase-activating polypeptide gene promoters in a dose-dependent manner. The interference with the transcriptional activation was dependent upon the presence of polyQ, the strength of which was increased as the length of polyQ stretches was expanded. Thus, polyQ interferes with the activity-dependent transcription in a polyQ-length-dependent manner, which may correspond to the severity of polyglutamine diseases.
KW - Activity-dependent transcription
KW - BDNF
KW - Calcium
KW - DRPLA
KW - PACAP
KW - Polyglutamine
UR - http://www.scopus.com/inward/record.url?scp=21344439060&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2005.06.032
DO - 10.1016/j.bbrc.2005.06.032
M3 - 学術論文
C2 - 15979572
AN - SCOPUS:21344439060
SN - 0006-291X
VL - 333
SP - 1241
EP - 1248
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -