Structure and function of the transcription factor AREC3
Structure and function of the transcription factor AREC3
批准号:
07670152
负责人:
KAWAKAMI Kiyoshi
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
项目状态:
已结题
起止时间:
1995 至 1996
中文摘要
1.从小鼠骨骼肌基因文库中克隆了三种编码AREC3/Six4蛋白的基因。序列分析表明,AREC3是一个新的六人基因家族成员,具有同源结构域和六个结构域作为保守结构域。这两个结构域都是特异DNA结合所必需的,潜在的反式激活结构域位于C末端。成肌细胞系C2C12在分化过程中,胞浆内有AREC3蛋白的产生。在大鼠出生后的视网膜形成过程中,基因产物的表达模式发生了巨大的变化。这些观察结果表明该基因参与了发育和分化过程。其他6个家族成员SIX2、Six3和Six5的cDNAs是从小鼠视网膜cDNA文库中分离得到的。原位杂交结果表明这些基因在视网膜中均有表达。同源结构域和六结构域是一个特异的dna结合域,其dna结合特异性在…中是保守的。更多SIX2、Six4和Six5.3。用免疫组织化学方法分析AREC3蛋白在新生大鼠视网膜和成年大鼠脑内的分布。在PND(出生后第1天),AREC3位于神经节细胞的胞核,在PND4,除PND1外,蛋白表达在内核层,在PND7,表达在内核层的外细胞。PND13在神经节细胞中的表达由胞核移至胞浆,外段和内段均有表达。PND20后,未观察到核内分布。在大鼠脑内,AREC3蛋白主要分布在海马区和梨状皮质的胞核中,其mRNA主要分布在胞浆中。在小鼠胚胎中,从E9.5期开始在神经元细胞核中检测到AREC3蛋白。结果表明,AREC3在神经元和视网膜的分化和发育过程中起重要作用。较少
英文摘要
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
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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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作者:
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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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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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Ikeda,K.: ""DNA binding through distinct domains of zinc-finger-homeodomain protein AREB6 has different effects on gene transcription."" Eur.J.Biochem.233. 73-82 (1995)
Ikeda,K.:“通过锌指同源结构域蛋白 AREB6 的不同结构域进行 DNA 结合对基因转录具有不同的影响。”Eur.J.Biochem.233。
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通讯作者:
Muto,S.: ""Differential regulation of Na^+-K^+-ATPase gene expression by corticosteroids in vascular smooth muscle cells."" Am.J.Physiol.270. C731-C739 (1996)
Muto,S.:“血管平滑肌细胞中皮质类固醇对 Na^-K^-ATP 酶基因表达的差异调节。”Am.J.Physiol.270。
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共 19 条
Physiological function of Na pumpα3 subunit gene and involvement in pathophysiology of dystonia parkinsonism.
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批准号:21590239
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
-
财政年份:2009
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负责人:KAWAKAMI Kiyoshi
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依托单位:
Principle of organogenesis derived from neural crest cells
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批准号:18390061
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.92万
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财政年份:2006
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负责人:KAWAKAMI Kiyoshi
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依托单位:
Developmental Program and Genetic Disease by Six family genes.
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批准号:12470029
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$9.09万
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财政年份:2000
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负责人:KAWAKAMI Kiyoshi
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依托单位:
Function of DMAHP/Six5 gene and the involvement in myotonic dystrophy
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批准号:10670143
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.73万
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财政年份:1998
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负责人:KAWAKAMI Kiyoshi
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依托单位:
Regulation of Na, K-ATPase in renal, cardiac, pulmonaly disease
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批准号:07044289
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$2.75万
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财政年份:1995
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负责人:KAWAKAMI Kiyoshi
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依托单位:
Study on oncoimmunology in carrier children of HTLV-I
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批准号:07670880
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.54万
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财政年份:1995
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负责人:KAWAKAMI Kiyoshi
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依托单位:
Mechanism of Regulation of Sodium Pump Gane Expressions in Muscle Differentiation
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批准号:04670152
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.41万
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财政年份:1992
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负责人:KAWAKAMI Kiyoshi
-
依托单位:
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-
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批准号:04670608
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.41万
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财政年份:1992
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负责人:KAWAKAMI Kiyoshi
-
依托单位:
海外基金