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1
Identification of a second human acetyl-CoA carboxylase gene.第二种人类乙酰辅酶A羧化酶基因的鉴定。
Biochem J. 1996 Jun 15;316 ( Pt 3)(Pt 3):915-22. doi: 10.1042/bj3160915.
2
Cloning of human acetyl-CoA carboxylase cDNA.人乙酰辅酶A羧化酶cDNA的克隆
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Human acetyl-CoA carboxylase: characterization, molecular cloning, and evidence for two isoforms.人乙酰辅酶A羧化酶:特性、分子克隆及两种同工型的证据。
Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):4011-5. doi: 10.1073/pnas.92.9.4011.
4
Human acetyl-CoA carboxylase 2. Molecular cloning, characterization, chromosomal mapping, and evidence for two isoforms.人乙酰辅酶A羧化酶2。分子克隆、特性分析、染色体定位及两种同工型的证据。
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Elucidation of a promoter activity that directs the expression of acetyl-CoA carboxylase alpha with an alternative N-terminus in a tissue-restricted fashion.对一种启动子活性的阐释,该启动子活性以组织特异性方式指导具有可变N端的乙酰辅酶A羧化酶α的表达。
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Plastid-localized acetyl-CoA carboxylase of bread wheat is encoded by a single gene on each of the three ancestral chromosome sets.面包小麦中质体定位的乙酰辅酶A羧化酶由三个祖先染色体组中每个组的单个基因编码。
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Genomic distribution of three promoters of the bovine gene encoding acetyl-CoA carboxylase alpha and evidence that the nutritionally regulated promoter I contains a repressive element different from that in rat.编码乙酰辅酶A羧化酶α的牛基因的三个启动子的基因组分布以及营养调控启动子I含有与大鼠不同的抑制元件的证据。
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Acetyl-CoA carboxylase 1 and 2 inhibition ameliorates steatosis and hepatic fibrosis in a MC4R knockout murine model of nonalcoholic steatohepatitis.乙酰辅酶 A 羧化酶 1 和 2 的抑制作用可改善 MC4R 基因敲除非酒精性脂肪性肝炎小鼠模型的脂肪变性和肝纤维化。
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本文引用的文献

1
Rat heart expresses two forms of mitochondrial carnitine palmitoyltransferase I. The minor component is identical to the liver enzyme.大鼠心脏表达两种形式的线粒体肉碱棕榈酰转移酶I。次要成分与肝脏中的酶相同。
J Biol Chem. 1994 Jul 22;269(29):18712-5.
2
Identification of human acetyl-CoA carboxylase isozymes in tissue and in breast cancer cells.人体组织及乳腺癌细胞中人类乙酰辅酶A羧化酶同工酶的鉴定
Int J Biochem. 1994 Apr;26(4):589-94. doi: 10.1016/0020-711x(94)90018-3.
3
Unique structural features and differential phosphorylation of the 280-kDa component (isozyme) of rat liver acetyl-CoA carboxylase.大鼠肝脏乙酰辅酶A羧化酶280-kDa组分(同工酶)的独特结构特征和差异磷酸化作用
J Biol Chem. 1994 May 20;269(20):14438-45.
4
Hepatic 5'-AMP-activated protein kinase: zonal distribution and relationship to acetyl-CoA carboxylase activity in varying nutritional states.肝脏5'-AMP激活蛋白激酶:不同营养状态下的区域分布及其与乙酰辅酶A羧化酶活性的关系。
Arch Biochem Biophys. 1994 Feb 1;308(2):413-9. doi: 10.1006/abbi.1994.1058.
5
Cloning of human acetyl-CoA carboxylase cDNA.人乙酰辅酶A羧化酶cDNA的克隆
Eur J Biochem. 1994 Jan 15;219(1-2):297-306. doi: 10.1111/j.1432-1033.1994.tb19941.x.
6
Acetyl-CoA carboxylase regulation of fatty acid oxidation in the heart.心脏中乙酰辅酶A羧化酶对脂肪酸氧化的调节
J Biol Chem. 1993 Dec 5;268(34):25836-45.
7
Human acetyl-CoA carboxylase: characterization, molecular cloning, and evidence for two isoforms.人乙酰辅酶A羧化酶:特性、分子克隆及两种同工型的证据。
Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):4011-5. doi: 10.1073/pnas.92.9.4011.
8
Catalytic subunits of the porcine and rat 5'-AMP-activated protein kinase are members of the SNF1 protein kinase family.猪和大鼠5'-AMP激活蛋白激酶的催化亚基是SNF1蛋白激酶家族的成员。
Biochim Biophys Acta. 1995 Apr 6;1266(1):73-82. doi: 10.1016/0167-4889(94)00222-z.
9
A method for isolation of intact, translationally active ribonucleic acid.一种分离完整的、具有翻译活性的核糖核酸的方法。
DNA. 1983;2(4):329-35. doi: 10.1089/dna.1983.2.329.
10
Localization of the gene for acetyl-CoA carboxylase to human chromosome 17.乙酰辅酶A羧化酶基因在人类第17号染色体上的定位。
Cytogenet Cell Genet. 1988;48(3):190-2. doi: 10.1159/000132623.

第二种人类乙酰辅酶A羧化酶基因的鉴定。

Identification of a second human acetyl-CoA carboxylase gene.

作者信息

Widmer J, Fassihi K S, Schlichter S C, Wheeler K S, Crute B E, King N, Nutile-McMenemy N, Noll W W, Daniel S, Ha J, Kim K H, Witters L A

机构信息

Department of Medicine, Dartmouth Medical School, Hanover NH 03755, USA.

出版信息

Biochem J. 1996 Jun 15;316 ( Pt 3)(Pt 3):915-22. doi: 10.1042/bj3160915.

DOI:10.1042/bj3160915
PMID:8670171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1217437/
Abstract

Acetyl-CoA carboxylase (ACC), an important enzyme in fatty acid biosynthesis and a regulator of fatty acid oxidation, is present in at least two isoenzymic forms in rat and human tissues. Previous work has established the existence of a 265,000 Da enzyme in both the rat and human (RACC265; HACC265) and a higher-molecular-mass species (275,000-280,000 Da) in the same species (RACC280; HACC275). An HACC265 gene has previously been localized to chromosome 17. In the present study, we report cloning of a partial-length human cDNA sequence which appears to correspond to HACC275 and its rat homologue, RACC280, as judged by mRNA tissue distribution and cell-specific regulation of mRNA/protein expression. The gene encoding this isoenzymic form of ACC has been localized to the long arm of human chromosome 12. Thus, ACC is represented in a multigene family in both rodents and humans. The newly discovered human gene and its rat homologue appear to be under different regulatory control to the HACC265 gene, as judged by tissue-specific expression in vivo and by independent modulation in cultured cells in vitro.

摘要

乙酰辅酶A羧化酶(ACC)是脂肪酸生物合成中的一种重要酶,也是脂肪酸氧化的调节因子,在大鼠和人类组织中至少以两种同工酶形式存在。先前的研究已证实大鼠和人类体内均存在一种265,000道尔顿的酶(RACC265;HACC265),且同一物种中还存在一种分子量更高的酶(275,000 - 280,000道尔顿)(RACC280;HACC275)。先前已将HACC265基因定位到17号染色体。在本研究中,我们报告了一个部分长度的人类cDNA序列的克隆,根据mRNA组织分布以及mRNA/蛋白质表达的细胞特异性调控判断,该序列似乎对应于HACC275及其大鼠同源物RACC280。编码这种ACC同工酶形式的基因已定位到人类12号染色体长臂。因此,ACC在啮齿动物和人类中均由一个多基因家族所代表。根据体内组织特异性表达以及体外培养细胞中的独立调控判断,新发现的人类基因及其大鼠同源物似乎受到与HACC265基因不同的调控。