Structure and function of the transcription factor AREC3
转录因子AREC3的结构和功能
基本信息
- 批准号:07670152
- 负责人:
- 金额:$ 1.66万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1995
- 资助国家:日本
- 起止时间:1995 至 1996
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1. Three species of cDNA encoding AREC3/Six4 protein has been cloned from mouse skeletal muscle cDNA library. Sequence analysis revealed that the AREC3 is a member of new gene family of Six which has homeodomain and sixdomain as conserved domains. Both of the domains are necessary for specific DNA binding, and potential transactivation domain resides in the C terminal portion. During the differentiation of myoblast cell line C2C12, the productio of AREC3 protein is induced in the cytoplasm. During postnatal retina formation in rat, the expression pattern of the gene product varies dramatically. These observations suggest that the gene is involved in development and differentiation process.2. Other members of Six family genes, Six2, Six3 and Six5 cDNAs were isolated from mouse retina cDNA library. These genes were shown to be expressed in retina by in situ hybridization. Homeodomain and sixdomain function as a specific DNA binding domain, and the DNA binding specificity was conserved am … More ong Six2, Six4 and Six5.3. The distribution of AREC3 protein was analyzed by immunohistochemistry in newborn the rat retina and in the adult rat brain. In PND (postnatal day)1, the AREC3 resided in the nucleus of ganglion cells, in PND4, in addition to PND1, the protein was expressed in the inner nuclear layr and in PND7, the expression was observed in outer cells of the inner nuclear layr. In PND13, the expression was moved from the nucleus to the cytoplasm in ganglion cells, and the protein was expressed in outer segment and inner segment. After PND20, no distribution in the nucleus was observed. In rat brain, AREC3 protein was observed in the cell nucleus in hippocampus and in the piriform cortex and the mRNA was observed in the cytoplasm.4. In the mouse embryo, the AREC3 protein was detected in the nucleus of neuronal cells from stage E9.5. The production peaks at E10.5 to E11.5 and then gradually declined to undetectable level at E14.5These results indicates that the AREC3 plays an important role in differentiation and development of neuron and retina. Less
1.从小鼠骨骼肌cDNA文库中克隆了三种编码AREC3/Six4蛋白的cDNA,序列分析表明AREC3是Six新基因家族的成员,该家族具有同源结构域和six结构域这两个结构域。特异性 DNA 结合所必需的,并且潜在的反式激活结构域位于 C 末端部分。 在成肌细胞系 C2C12 的分化过程中,AREC3 蛋白的产生被诱导。在大鼠出生后视网膜形成过程中,该基因产物的表达模式变化很大。2.分离了6个家族基因的其他成员Six2、Six3和Six5 cDNA。来自小鼠视网膜 cDNA 文库的这些基因通过原位杂交显示在视网膜中表达,并且 Sixdomain 充当特定的 DNA 结合域,并且 DNA 结合特异性在 Six2、Six4 和 Six4 中保持不变。 Six5.3.通过免疫组织化学分析新生大鼠视网膜和成年大鼠大脑中AREC3蛋白的分布。在PND(出生后)1中,除了PND1之外,AREC3还存在于神经节细胞的细胞核中。 ,该蛋白在内核层表达,在PND7中,在内核层的外细胞中观察到表达,在PND13中,表达从细胞核转移到细胞质。 PND20后,在神经节细胞中未观察到AREC3蛋白在细胞核中的分布,且在外节和内节中没有观察到AREC3蛋白的分布,并且在梨状皮层中观察到AREC3蛋白的mRNA表达。 4.在小鼠胚胎中,E9.5期神经元细胞核中检测到AREC3蛋白,在E10.5至E11.5时产量达到峰值,随后逐渐下降。在E14.5处检测不到的水平这些结果表明AREC3在神经元和视网膜的分化和发育中发挥着重要作用。
项目成果
期刊论文数量(24)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Kobayashi, M.: "ATF-1/CREB heterodimer is involved in constitutive expression of the housekeeping Na, K-ATPase alpha1 subunit gene." Nucl.Acids Res.23. 2848-2855 (1995)
Kobayashi, M.:“ATF-1/CREB 异二聚体参与管家 Na、K-ATP 酶 α1 亚基基因的组成型表达。”
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- 发表时间:
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- 影响因子:0
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- 通讯作者:
Kawakami,K: ""Structure,function and expression of a murine homeobox protein AREC3,a homologue of Drosophila sine oculis gene product,and implicaion in development."" Nucl.Acids Res.24. 303-310 (1996)
Kawakami,K:“鼠同源盒蛋白 AREC3(果蝇正眼基因产物的同源物)的结构、功能和表达及其在发育中的意义。”Nucl.Acids Res.24。
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- 期刊:
- 影响因子:0
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Kobayashi, M.: "Phosphorylation of ATF-1 enhances its DNA binding and transcription of the Na, K-ATPase alpha1 subunit gene promoter." Nucl.Acids Res.25. 877-882 (1997)
Kobayashi, M.:“ATF-1 的磷酸化增强了其 DNA 结合以及 Na、K-ATPase α1 亚基基因启动子的转录。”
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- 发表时间:
- 期刊:
- 影响因子:0
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- 通讯作者:
Kawakami,K.: ""Characterization of the core promoter of the Na^+/K^+-ATPase α1 subunit gene : Elements required for transcription by RNA polymerase II and III in vitro."" Eur.J.Biochem.237. 440-446 (1996)
Kawakami, K.:“Na^+/K^+-ATPase α1 亚基基因核心启动子的表征:RNA 聚合酶 II 和 III 体外转录所需的元件。”Eur.J.Biochem.237。 440-446 (1996)
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- 影响因子:0
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Ohtaka, A.: "Hyperosmolarity stimulates Na, K-ATPase gene expression in inner medullary collecting duct cells." Am.J.Physiol. 270. F728-F738 (1996)
Ohtaka, A.:“高渗透压刺激内髓集合管细胞中 Na、K-ATP 酶基因的表达。”
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KAWAKAMI Kiyoshi其他文献
KAWAKAMI Kiyoshi的其他文献
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{{ truncateString('KAWAKAMI Kiyoshi', 18)}}的其他基金
Physiological function of Na pumpα3 subunit gene and involvement in pathophysiology of dystonia parkinsonism.
Na泵α3亚基基因的生理功能及其参与肌张力障碍帕金森病的病理生理学。
- 批准号:
21590239 - 财政年份:2009
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Principle of organogenesis derived from neural crest cells
神经嵴细胞的器官发生原理
- 批准号:
18390061 - 财政年份:2006
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Developmental Program and Genetic Disease by Six family genes.
六个家族基因的发育计划和遗传疾病。
- 批准号:
12470029 - 财政年份:2000
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Function of DMAHP/Six5 gene and the involvement in myotonic dystrophy
DMAHP/Six5基因的功能及其与强直性肌营养不良的关系
- 批准号:
10670143 - 财政年份:1998
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Regulation of Na, K-ATPase in renal, cardiac, pulmonaly disease
肾脏、心脏、肺部疾病中 Na、K-ATP 酶的调节
- 批准号:
07044289 - 财政年份:1995
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for international Scientific Research
Study on oncoimmunology in carrier children of HTLV-I
HTLV-I携带者儿童肿瘤免疫学研究
- 批准号:
07670880 - 财政年份:1995
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Mechanism of Regulation of Sodium Pump Gane Expressions in Muscle Differentiation
钠泵 Gane 表达在肌肉分化中的调控机制
- 批准号:
04670152 - 财政年份:1992
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
Study on mother-to-child transmission of human T-lymphotropic virus type I.-Guidance for safe and proper way of breast feeding for carrier mother-
人类嗜T淋巴细胞病毒I型母婴传播研究-携带者母亲安全正确母乳喂养指南-
- 批准号:
04670608 - 财政年份:1992
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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