• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人铜蓝蛋白基因的精细结构

Fine structure of the human ceruloplasmin gene.

作者信息

Daimon M, Yamatani K, Igarashi M, Fukase N, Kawanami T, Kato T, Tominaga M, Sasaki H

机构信息

Third Department of Internal Medicine, Yamagata University, School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1995 Mar 28;208(3):1028-35. doi: 10.1006/bbrc.1995.1437.

DOI:10.1006/bbrc.1995.1437
PMID:7702601
Abstract

We characterized the genomic region corresponding to the human ceruloplasmin cDNA previously reported. Using PCR-direct sequencing methods, we determined precise intron/exon boundaries and intron-exon composition of the gene in the region. The gene region spanned about 50 kb and was composed of 19 exons and 18 introns. The lengths of exons and introns range from 107 to over 267 bp and from 0.44 to 10.0 kb, respectively. The translation initiation codon and the termination codon were located in exons 1 and 19, respectively. The nucleotide sequences of the introns were also determined in the region around the intron/exon boundaries for 24-220 bp. All the sequences around the intron/exon boundaries were consistent with the 5' and 3' consensus sequences for splice junctions of transcribed genes. Putative lariat sequences were identified between -17 and -42 nucleotides from the 3' splice junction for all 18 introns.

摘要

我们对先前报道的与人类铜蓝蛋白cDNA相对应的基因组区域进行了特征分析。使用聚合酶链反应直接测序方法,我们确定了该区域基因精确的内含子/外显子边界和内含子-外显子组成。该基因区域跨度约50 kb,由19个外显子和18个内含子组成。外显子和内含子的长度分别为107至超过267 bp以及0.44至10.0 kb。翻译起始密码子和终止密码子分别位于外显子1和19中。还测定了内含子/外显子边界周围24 - 220 bp区域的内含子核苷酸序列。内含子/外显子边界周围的所有序列均与转录基因剪接连接的5'和3'共有序列一致。在所有18个内含子的3'剪接连接下游- 17至- 42个核苷酸之间鉴定出了假定的套索序列。

相似文献

1
Fine structure of the human ceruloplasmin gene.人铜蓝蛋白基因的精细结构
Biochem Biophys Res Commun. 1995 Mar 28;208(3):1028-35. doi: 10.1006/bbrc.1995.1437.
2
Fine structure of the human translocation protein 1 (HTP1/TLOC1) gene.人类易位蛋白1(HTP1/TLOC1)基因的精细结构
IUBMB Life. 1999 Dec;48(6):619-24. doi: 10.1080/713803565.
3
Genomic organization of the human beta-catenin gene (CTNNB1).人类β-连环蛋白基因(CTNNB1)的基因组结构
Genomics. 1996 Mar 15;32(3):413-24. doi: 10.1006/geno.1996.0136.
4
Molecular cloning and organization of the coding region of the human norepinephrine transporter gene.人类去甲肾上腺素转运体基因编码区的分子克隆与组织
Biochem Biophys Res Commun. 1995 Oct 24;215(3):1145-50. doi: 10.1006/bbrc.1995.2582.
5
Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.在人类肌营养不良蛋白基因中鉴定出一个新的首个外显子以及一个位于距离最近已知启动子上游超过500 kb处的新启动子。
J Clin Invest. 1994 Sep;94(3):1037-42. doi: 10.1172/JCI117417.
6
[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].[通过新型人类基因的电子克隆和实验验证对NCBI人类基因数据库中出现的模型参考序列的一些错误进行分析、鉴定和校正]
Yi Chuan Xue Bao. 2004 May;31(5):431-43.
7
Molecular cloning and structural characterization of the human histidase gene (HAL).人类组氨酸酶基因(HAL)的分子克隆与结构表征
Genomics. 1995 Sep 1;29(1):98-104. doi: 10.1006/geno.1995.1219.
8
Structure and organization of the human glucose phosphate isomerase gene (GPI).人类葡萄糖磷酸异构酶基因(GPI)的结构与组织
Genomics. 1995 Sep 1;29(1):261-5. doi: 10.1006/geno.1995.1241.
9
The gene for human protein Z is localized to chromosome 13 at band q34 and is coded by eight regular exons and one alternative exon.人类蛋白Z基因定位于13号染色体q34带,由8个常规外显子和1个可变外显子编码。
Biochemistry. 1998 May 12;37(19):6838-46. doi: 10.1021/bi972002a.
10
The exon-intron organization of the human erythroid beta-spectrin gene.人类红细胞β-血影蛋白基因的外显子-内含子结构
Genomics. 1993 Oct;18(1):118-25. doi: 10.1006/geno.1993.1434.

引用本文的文献

1
Abnormalities in Copper Status Associated with an Elevated Risk of Parkinson's Phenotype Development.与帕金森病表型发展风险升高相关的铜状态异常。
Antioxidants (Basel). 2023 Aug 22;12(9):1654. doi: 10.3390/antiox12091654.
2
Molecular Functions of Ceruloplasmin in Metabolic Disease Pathology.铜蓝蛋白在代谢性疾病病理学中的分子功能
Diabetes Metab Syndr Obes. 2022 Mar 3;15:695-711. doi: 10.2147/DMSO.S346648. eCollection 2022.
3
The Crossroads between Host Copper Metabolism and Influenza Infection.宿主铜代谢与流感感染的交汇点。
Int J Mol Sci. 2021 May 23;22(11):5498. doi: 10.3390/ijms22115498.
4
Does Ceruloplasmin Defend Against Neurodegenerative Diseases?铜蓝蛋白能预防神经退行性疾病吗?
Curr Neuropharmacol. 2019;17(6):539-549. doi: 10.2174/1570159X16666180508113025.
5
Bioinformatic Characterization of Genes and Proteins Involved in Blood Clotting in Lampreys.七鳃鳗血液凝固相关基因和蛋白质的生物信息学特征分析
J Mol Evol. 2015 Oct;81(3-4):121-30. doi: 10.1007/s00239-015-9701-0. Epub 2015 Oct 5.
6
Aceruloplasminemia: a case report.无铜蓝蛋白血症:一例报告。
Intern Emerg Med. 2008 Dec;3(4):395-9. doi: 10.1007/s11739-008-0150-2. Epub 2008 Apr 12.
7
Genomic evidence for a simpler clotting scheme in jawless vertebrates.无颌脊椎动物中更简单凝血机制的基因组证据。
J Mol Evol. 2008 Feb;66(2):185-96. doi: 10.1007/s00239-008-9074-8. Epub 2008 Feb 19.
8
A third approach to gene prediction suggests thousands of additional human transcribed regions.第三种基因预测方法表明,人类转录区域还有数千个。
PLoS Comput Biol. 2006 Mar;2(3):e18. doi: 10.1371/journal.pcbi.0020018. Epub 2006 Mar 17.
9
Iron in neurodegenerative disorders.神经退行性疾病中的铁
Neurotox Res. 2002 Nov-Dec;4(7-8):637-653. doi: 10.1080/1029842021000045444.
10
Delayed translational silencing of ceruloplasmin transcript in gamma interferon-activated U937 monocytic cells: role of the 3' untranslated region.γ干扰素激活的U937单核细胞中铜蓝蛋白转录本的延迟翻译沉默:3'非翻译区的作用
Mol Cell Biol. 1999 Oct;19(10):6898-905. doi: 10.1128/MCB.19.10.6898.