Identification of a negative regulatory DNA element for neuronal BC1 RNA expression by RNA polymerase III

被引:10
作者
Kobayashi, S [1 ]
Kamo, S [1 ]
Ohmae, A [1 ]
Agui, K [1 ]
Li, YM [1 ]
Anzai, K [1 ]
机构
[1] Nihon Univ, Coll Pharm, Dept Biochem, Chiba 2748555, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1493卷 / 1-2期
关键词
neuronal BC1 RNA; promoter; in vitro transcription system; negative regulatory element;
D O I
10.1016/S0167-4781(00)00175-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BC1 RNA is a neuronal cell-specific RNA polymerase III (Pol III) transcript. The BC1 RNA gene has plural types of Pol III promoters, in addition to which an E-box sequence (E2 site) acts as a transcriptional activator, which is recognized by a brain-specific protein(s). Using an in vitro transcription system, we found that the upstream region of the BC1 RNA gene contained a sequence that interfered with the activity of the E-box element in a distance-independent manner. A tandem repeat within this sequence, which was weakly homologous with the neuron-restrictive silencer element (NRSE) found in the Pol II system, was recognized by a brain nuclear protein. Consistently, the transcriptional activity increased by deleting the tandem repeat sequence. We called this BC1 RNA-repressing element BCRE. The DNA-binding specificities of BCRE-binding protein differed from that of NRSE-binding protein (NRSF). A similar protein with an ability to bind to BCRE was also found in liver and kidney. Furthermore, the glutamate analog kainic acid increased the DNA-binding of both E2 site-binding protein and BCRE-binding protein, and then the levels of BC1 RNA also increased transiently. Our results suggested that both positive and negative regulatory elements contribute to neuronal BC1 RNA expression. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:142 / 150
页数:9
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