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人脑海马体β - 肾上腺素能受体的克隆与序列分析。与啮齿动物、禽类β - 受体及猪毒蕈碱受体的进化关系。

Cloning and sequence analysis of the human brain beta-adrenergic receptor. Evolutionary relationship to rodent and avian beta-receptors and porcine muscarinic receptors.

作者信息

Chung F Z, Lentes K U, Gocayne J, Fitzgerald M, Robinson D, Kerlavage A R, Fraser C M, Venter J C

出版信息

FEBS Lett. 1987 Jan 26;211(2):200-6. doi: 10.1016/0014-5793(87)81436-9.

DOI:10.1016/0014-5793(87)81436-9
PMID:3026848
Abstract

Two cDNA clones, lambda-CLFV-108 and lambda-CLFV-119, encoding for the beta-adrenergic receptor, have been isolated from a human brain stem cDNA library. One human genomic clone, LCV-517 (20 kb), was characterized by restriction mapping and partial sequencing. The human brain beta-receptor consists of 413 amino acids with a calculated Mr of 46480. The gene contains three potential glucocorticoid receptor-binding sites. The beta-receptor expressed in human brain was homology with rodent (88%) and avian (52%) beta-receptors and with porcine muscarinic cholinergic receptors (31%), supporting our proposal [(1984) Proc. Natl. Acad. Sci. USA 81, 272 276] that adrenergic and muscarinic cholinergic receptors are structurally related. This represents the first cloning of a neurotransmitter receptor gene from human brain.

摘要

已从人脑干cDNA文库中分离出两个编码β-肾上腺素能受体的cDNA克隆,λ-CLFV-108和λ-CLFV-119。通过限制性酶切图谱分析和部分测序对一个人基因组克隆LCV-517(20kb)进行了表征。人脑中的β-受体由413个氨基酸组成,计算分子量为46480。该基因包含三个潜在的糖皮质激素受体结合位点。在人脑中表达的β-受体与啮齿动物(88%)和禽类(52%)的β-受体以及猪毒蕈碱胆碱能受体(31%)具有同源性,这支持了我们之前的提议[(1984年)《美国国家科学院院刊》81, 272 - 276],即肾上腺素能和毒蕈碱胆碱能受体在结构上相关。这是首次从人脑中克隆神经递质受体基因。

相似文献

1
Cloning and sequence analysis of the human brain beta-adrenergic receptor. Evolutionary relationship to rodent and avian beta-receptors and porcine muscarinic receptors.人脑海马体β - 肾上腺素能受体的克隆与序列分析。与啮齿动物、禽类β - 受体及猪毒蕈碱受体的进化关系。
FEBS Lett. 1987 Jan 26;211(2):200-6. doi: 10.1016/0014-5793(87)81436-9.
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Primary structure of rat cardiac beta-adrenergic and muscarinic cholinergic receptors obtained by automated DNA sequence analysis: further evidence for a multigene family.通过自动DNA序列分析获得的大鼠心脏β-肾上腺素能和毒蕈碱胆碱能受体的一级结构:多基因家族的进一步证据。
Proc Natl Acad Sci U S A. 1987 Dec;84(23):8296-300. doi: 10.1073/pnas.84.23.8296.
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引用本文的文献

1
Adrenoceptors: Receptors, Ligands and Their Clinical Uses, Molecular Pharmacology and Assays.肾上腺素能受体:受体、配体及其临床用途,分子药理学和检测。
Handb Exp Pharmacol. 2024;285:55-145. doi: 10.1007/164_2024_713.
2
Enhancement of murine cardiac chronotropy by the molecular transfer of the human beta2 adrenergic receptor cDNA.通过人β2肾上腺素能受体cDNA的分子转移增强小鼠心脏变时性
J Clin Invest. 1998 Jan 15;101(2):337-43. doi: 10.1172/JCI1330.
3
Respective degree of expression of beta 1-, beta 2- and beta 3-adrenoceptors in human brown and white adipose tissues.
人棕色和白色脂肪组织中β1-、β2-和β3-肾上腺素能受体的各自表达程度。
Br J Pharmacol. 1996 Jun;118(4):929-34. doi: 10.1111/j.1476-5381.1996.tb15488.x.
4
Expression of beta 1- and beta 3-adrenergic-receptor messages and adenylate cyclase beta-adrenergic response in bovine perirenal adipose tissue during its transformation from brown into white fat.牛肾周脂肪组织从棕色脂肪转变为白色脂肪过程中β1-和β3-肾上腺素能受体信息的表达及腺苷酸环化酶β-肾上腺素能反应
Biochem J. 1994 Jan 1;297 ( Pt 1)(Pt 1):93-7. doi: 10.1042/bj2970093.
5
The evolutionary divergence of neurotransmitter receptors and second-messenger pathways.神经递质受体与第二信使途径的进化分歧。
J Mol Evol. 1995 Jul;41(1):85-97. doi: 10.1007/BF00174044.
6
Genetic mapping of adrenergic receptor genes in humans.人类肾上腺素能受体基因的遗传图谱
J Mol Med (Berl). 1995 Jun;73(6):299-306. doi: 10.1007/BF00231616.
7
Down-regulation of beta-adrenergic receptors: agonist-induced reduction in receptor mRNA levels.β-肾上腺素能受体的下调:激动剂诱导的受体mRNA水平降低。
Proc Natl Acad Sci U S A. 1988 Jul;85(14):5021-5. doi: 10.1073/pnas.85.14.5021.
8
The structure and mechanism of neurotransmitter receptors. Implications for the structure and function of the central nervous system.神经递质受体的结构与机制。对中枢神经系统结构和功能的影响。
Biochem J. 1988 Jan 15;249(2):309-18. doi: 10.1042/bj2490309.
9
Regulation of beta-adrenergic receptors by "permissive" hormones: glucocorticoids increase steady-state levels of receptor mRNA.“允许性”激素对β-肾上腺素能受体的调节:糖皮质激素可提高受体mRNA的稳态水平。
Proc Natl Acad Sci U S A. 1988 Nov;85(22):8415-9. doi: 10.1073/pnas.85.22.8415.
10
Site-directed mutagenesis of human beta-adrenergic receptors: substitution of aspartic acid-130 by asparagine produces a receptor with high-affinity agonist binding that is uncoupled from adenylate cyclase.人β-肾上腺素能受体的定点诱变:将天冬氨酸-130替换为天冬酰胺可产生一种与腺苷酸环化酶解偶联的具有高亲和力激动剂结合能力的受体。
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5478-82. doi: 10.1073/pnas.85.15.5478.