• 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

Complementary DNA sequence and chromosomal localization of xpg, the mouse counterpart of human repair gene XPG/ERCC5.

作者信息

Harada Y N, Matsuda Y, Shiomi N, Shiomi T

机构信息

Division of Genetics, National Institute of Radiological Sciences, Chiba, Japan.

出版信息

Genomics. 1995 Jul 1;28(1):59-65. doi: 10.1006/geno.1995.1106.

DOI:10.1006/geno.1995.1106
PMID:7590748
Abstract

We have molecularly cloned and sequenced the mouse counterpart of the human repair gene XPG/ERCC5 cDNA. The mouse xpg cDNA had a single long open reading frame predicted to encode 1170 amino acid residues (predicted M(r) of 130,753). Northern blot analysis has been carried out to determine the size and tissue transcription specificity of the mouse xpg mRNA. The xpg gene expressed one species of transcript with 4.3 kb at similar levels in five mouse tissues examined. We have determined the chromosomal location of the xpg gene by both in situ hybridization and molecular linkage analysis. The xpg gene was localized at 2.3 cM proximal to the microsatellite locus D1Mit18 on the R-positive B band of mouse chromosome 1. By in situ hybridization with the mouse xpg probe, the rat homolog of the mouse xpg was localized on q22.3 band of rat chromosome 9, which has been known to have a conserved linkage homology to mouse chromosome 1. In the case of human, the XPG/ERCC5 gene has been reported to be assigned to human chromosome 13q32.3-q33.1, where any conserved linkage homology to mouse chromosome 1 has not been found so far. Thus, these results show new regions of conserved linkage homology among mouse chromosome 1, rat chromosome 9, and human chromosome 13q.

摘要

相似文献

1
Complementary DNA sequence and chromosomal localization of xpg, the mouse counterpart of human repair gene XPG/ERCC5.
Genomics. 1995 Jul 1;28(1):59-65. doi: 10.1006/geno.1995.1106.
2
cDNA cloning of a murine homologue of Drosophila single-minded, its mRNA expression in mouse development, and chromosome localization.果蝇单 minded 蛋白的小鼠同源物的 cDNA 克隆、其 mRNA 在小鼠发育过程中的表达及染色体定位
Biochem Biophys Res Commun. 1996 Jan 17;218(2):588-94. doi: 10.1006/bbrc.1996.0104.
3
[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.
4
Cloning, mapping, and tissue distribution of a human homologue of the mouse jerky gene product.小鼠震颤基因产物的人类同源物的克隆、定位及组织分布
Biochem Biophys Res Commun. 1997 Jul 18;236(2):389-95. doi: 10.1006/bbrc.1997.6935.
5
Molecular cloning and chromosomal localization of the mouse Gpr37 gene encoding an orphan G-protein-coupled peptide receptor expressed in brain and testis.编码在脑和睾丸中表达的孤儿G蛋白偶联肽受体的小鼠Gpr37基因的分子克隆及染色体定位。
Genomics. 1998 Nov 1;53(3):315-24. doi: 10.1006/geno.1998.5433.
6
Cloning, comparative mapping, and RNA expression of the mouse homologues of the Saccharomyces cerevisiae nucleotide excision repair gene RAD23.酿酒酵母核苷酸切除修复基因RAD23的小鼠同源物的克隆、比较定位及RNA表达
Genomics. 1996 Jan 1;31(1):20-7. doi: 10.1006/geno.1996.0004.
7
cDNA cloning and gene structure of a novel water channel expressed exclusively in human kidney: evidence for a gene cluster of aquaporins at chromosome locus 12q13.一种仅在人肾脏中表达的新型水通道的cDNA克隆及基因结构:染色体位点12q13上水通道蛋白基因簇的证据
Genomics. 1996 Aug 1;35(3):543-50. doi: 10.1006/geno.1996.0396.
8
Isolation and characterization of mouse Xrcc-1, a DNA repair gene affecting ligation.
Genomics. 1994 Jul 1;22(1):180-8. doi: 10.1006/geno.1994.1359.
9
Cloning of a complementary DNA encoding a new mouse B lymphocyte differentiation antigen, homologous to the human B1 (CD20) antigen, and localization of the gene to chromosome 19.一种与人类B1(CD20)抗原同源的、编码新的小鼠B淋巴细胞分化抗原的互补DNA的克隆,以及该基因在染色体19上的定位。
J Immunol. 1988 Dec 15;141(12):4388-94.
10
Human brain factor 1, a new member of the fork head gene family.人脑因子1,叉头基因家族的一个新成员。
Genomics. 1994 Jun;21(3):551-7. doi: 10.1006/geno.1994.1313.

引用本文的文献

1
A novel hairless mouse model on an atopic dermatitis-prone genetic background generated by receptor-mediated transgenesis.
Transgenic Res. 2008 Dec;17(6):1155-62. doi: 10.1007/s11248-008-9203-6. Epub 2008 Aug 7.
2
Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method.利用cDNA介导的基因敲入方法产生的Xpg突变小鼠鉴定导致科凯恩综合征发病的XPG区域。
Mol Cell Biol. 2004 May;24(9):3712-9. doi: 10.1128/MCB.24.9.3712-3719.2004.
3
Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene.在缺乏着色性干皮病G组基因的小鼠中,出生后生长发育迟缓、寿命缩短,并且细胞衰老和随后的永生化提前发生。
Mol Cell Biol. 1999 Mar;19(3):2366-72. doi: 10.1128/MCB.19.3.2366.
4
Molecular cloning and structural analysis of the functional mouse genomic XPG gene.功能性小鼠基因组XPG基因的分子克隆与结构分析
Mamm Genome. 1996 Sep;7(9):644-9. doi: 10.1007/s003359900198.