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从cDNA序列推导的加州电鳐乙酰胆碱受体β和δ亚基前体的一级结构。

Primary structures of beta- and delta-subunit precursors of Torpedo californica acetylcholine receptor deduced from cDNA sequences.

作者信息

Noda M, Takahashi H, Tanabe T, Toyosato M, Kikyotani S, Hirose T, Asai M, Takashima H, Inayama S, Miyata T, Numa S

出版信息

Nature. 1983 Jan 20;301(5897):251-5. doi: 10.1038/301251a0.

DOI:10.1038/301251a0
PMID:6687403
Abstract

The nicotinic acetylcholine receptor (AChR) from fish electric organ and mammalian skeletal muscle is the best characterized neurotransmitter receptor (reviewed in refs 1-3). The AChR from the electroplax of the ray Torpedo californica consists of five subunits present in a molar stoichiometry of alpha 2 beta gamma delta (refs 4-6); the apparent molecular weights of the alpha-, beta-, gamma- and delta-subunits are 40,000 (40K), 50K, 60K and 65K, respectively. Knowledge of the primary structures of these constituent polypeptides would facilitate the understanding of the molecular mechanism underlying the function of the neurotransmitter receptor. Recently, we have cloned cDNA for the alpha-subunit precursor of the T. californica AChR and have deduced the primary structure of this polypeptide from the nucleotide sequence of the cloned cDNA. Here we report the cloning and nucleotide analysis of cDNAs for the AChR beta- and delta-subunit precursors. The primary structures of the two polypeptides deduced from the cDNA sequences reveal conspicuous amino acid sequence homology among these and the alpha-subunits. The three subunits contain several highly conserved regions which may be essential for the receptor function or inter-subunit interaction.

摘要

鱼类电器官和哺乳动物骨骼肌中的烟碱型乙酰胆碱受体(AChR)是特征最为明确的神经递质受体(参考文献1 - 3中有综述)。电鳐加州电鳐(Torpedo californica)电板中的AChR由五个亚基组成,其摩尔化学计量比为α2βγδ(参考文献4 - 6);α、β、γ和δ亚基的表观分子量分别为40,000(40K)、50K、60K和65K。了解这些组成多肽的一级结构将有助于理解神经递质受体功能背后的分子机制。最近,我们克隆了加州电鳐AChRα亚基前体的cDNA,并从克隆的cDNA核苷酸序列推导了该多肽的一级结构。在此,我们报告AChRβ和δ亚基前体cDNA的克隆及核苷酸分析。从cDNA序列推导的这两种多肽的一级结构显示,它们与α亚基之间存在明显的氨基酸序列同源性。这三个亚基包含几个高度保守的区域,这些区域可能对受体功能或亚基间相互作用至关重要。

相似文献

1
Primary structures of beta- and delta-subunit precursors of Torpedo californica acetylcholine receptor deduced from cDNA sequences.从cDNA序列推导的加州电鳐乙酰胆碱受体β和δ亚基前体的一级结构。
Nature. 1983 Jan 20;301(5897):251-5. doi: 10.1038/301251a0.
2
Cloning and sequence analysis of calf cDNA and human genomic DNA encoding alpha-subunit precursor of muscle acetylcholine receptor.编码肌肉乙酰胆碱受体α亚基前体的小牛cDNA和人类基因组DNA的克隆与序列分析
Nature. 1983;305(5937):818-23. doi: 10.1038/305818a0.
3
Structural homology of Torpedo californica acetylcholine receptor subunits.加州电鳐乙酰胆碱受体亚基的结构同源性。
Nature. 1983 Apr 7;302(5908):528-32. doi: 10.1038/302528a0.
4
Cloning, sequencing and expression of cDNA for a novel subunit of acetylcholine receptor from calf muscle.小牛肌肉乙酰胆碱受体新亚基cDNA的克隆、测序及表达
Nature. 1985;315(6022):761-4. doi: 10.1038/315761a0.
5
Primary structure of delta subunit precursor of calf muscle acetylcholine receptor deduced from cDNA sequence.从cDNA序列推导小牛肌肉乙酰胆碱受体δ亚基前体的一级结构。
Eur J Biochem. 1985 May 15;149(1):5-13. doi: 10.1111/j.1432-1033.1985.tb08885.x.
6
Primary structure of gamma subunit precursor of calf-muscle acetylcholine receptor deduced from the cDNA sequence.从cDNA序列推导的小牛肌肉乙酰胆碱受体γ亚基前体的一级结构。
Eur J Biochem. 1984 Aug 15;143(1):109-15. doi: 10.1111/j.1432-1033.1984.tb08348.x.
7
Cloning and sequence analysis of human genomic DNA encoding gamma subunit precursor of muscle acetylcholine receptor.编码肌肉乙酰胆碱受体γ亚基前体的人类基因组DNA的克隆与序列分析。
Eur J Biochem. 1985 Jan 2;146(1):15-22. doi: 10.1111/j.1432-1033.1985.tb08614.x.
8
Primary structure of alpha-subunit precursor of Torpedo californica acetylcholine receptor deduced from cDNA sequence.从cDNA序列推导的加州电鳐乙酰胆碱受体α亚基前体的一级结构
Nature. 1982 Oct 28;299(5886):793-7. doi: 10.1038/299793a0.
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A universal oligonucleotide probe for acetylcholine receptor genes. Selection and sequencing of cDNA clones for the mouse muscle beta subunit.一种用于乙酰胆碱受体基因的通用寡核苷酸探针。小鼠肌肉β亚基cDNA克隆的筛选与测序。
J Biol Chem. 1986 Dec 15;261(35):16451-8.
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Molecular cloning of cDNA coding for the gamma subunit of Torpedo acetylcholine receptor.电鳐乙酰胆碱受体γ亚基编码cDNA的分子克隆
Proc Natl Acad Sci U S A. 1982 Jul;79(14):4466-70. doi: 10.1073/pnas.79.14.4466.

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