• 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

Canine COL4A3 and COL4A4: sequencing, mapping and genomic organization.

作者信息

Wiersma Anje C, Millon Lee V, Hestand Matthew S, Van Oost Bernard A, Bannasch Danika L

机构信息

Department of Animals, Science and Society, Faculty of Veterinary Medicine, Utrecht University, P.O. Box 80.166, 3508 TD, Utrecht, The Netherlands.

出版信息

DNA Seq. 2005 Aug;16(4):241-51. doi: 10.1080/10425170500136822.

DOI:10.1080/10425170500136822
PMID:16147883
Abstract

Canine alpha3 and alpha4 chains of collagen type IV genes (COL4A3 and COL4A4) are expressed in the renal glomerular basement membrane, where they provide a critical structural and functional matrix for other basement membrane components. These genes are candidates for hereditary nephritis (Alport syndrome) in several dog breeds (e.g. English Cocker Spaniel and Bull Terrier). Using RACE and PCR, the cDNA of both genes was cloned and sequenced. Both COL4A3 and COL4A4, as well as canine NPPC (Natriuretic Peptide Precursor C), were mapped to CFA25 using an RH panel. Conservation of the tight linkage of COL4A3 and COL4A4 as seen in human and mouse was verified in the dog. Intron-exon boundaries in both genes were determined by BLAST analysis of the Canis Familiaris Trace Archive. The elucidation of the cDNA sequences, genomic organization and the open reading frames of canine COL4A3 and COL4A4 provide the groundwork for screening these genes for mutations in hereditary nephritis in dogs.

摘要

相似文献

1
Canine COL4A3 and COL4A4: sequencing, mapping and genomic organization.
DNA Seq. 2005 Aug;16(4):241-51. doi: 10.1080/10425170500136822.
2
Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome.在奥尔波特综合征小鼠模型中胶原蛋白基因Col4a3和Col4a4的插入突变。
Genomics. 1999 Oct 15;61(2):113-24. doi: 10.1006/geno.1999.5943.
3
Evaluation of canine COL4A3 and COL4A4 as candidates for familial renal disease in the Norwegian elkhound.
J Hered. 2005;96(7):739-44. doi: 10.1093/jhered/esi068. Epub 2005 Jul 13.
4
Structure of the human type IV collagen COL4A6 gene, which is mutated in Alport syndrome-associated leiomyomatosis.人类IV型胶原蛋白COL4A6基因的结构,该基因在与奥尔波特综合征相关的平滑肌瘤病中发生突变。
Genomics. 1996 May 1;33(3):473-9. doi: 10.1006/geno.1996.0222.
5
[Approaches to detect the gene mutations in autosomal recessive Alport's syndrome: analysis of a family].[检测常染色体隐性遗传性奥尔波特综合征基因突变的方法:一个家系的分析]
Zhonghua Yi Xue Za Zhi. 2008 Feb 26;88(8):573-5.
6
Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog.犬类光感受器特异性视锥-视杆同源框(CRX)基因的克隆与特性分析及其作为犬类早发性光感受器疾病候选基因的评估
Mol Vis. 2002 Mar 22;8:79-84.
7
Alport syndrome. Molecular genetic aspects.奥尔波特综合征。分子遗传学方面。
Dan Med Bull. 2009 Aug;56(3):105-52.
8
Three novel COL4A4 mutations resulting in stop codons and their clinical effects in autosomal recessive Alport syndrome.导致终止密码子的三种新型COL4A4突变及其在常染色体隐性遗传性阿尔波特综合征中的临床效应
Hum Mutat. 2002 Oct;20(4):321-2. doi: 10.1002/humu.9065.
9
Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy.COL4A3+/-小鼠的慢性肾衰竭与寿命缩短:薄基底膜肾病的动物模型
J Am Soc Nephrol. 2006 Jul;17(7):1986-94. doi: 10.1681/ASN.2005101044. Epub 2006 Jun 14.
10
Alport syndrome and thin basement membrane nephropathy.奥尔波特综合征和薄基底膜肾病。
Nephron Clin Pract. 2007;106(2):c82-8. doi: 10.1159/000101802. Epub 2007 Jun 6.

引用本文的文献

1
Long-term follow-up of an Alport syndrome patient with a novel mutation of .一名患有新型突变的Alport综合征患者的长期随访
Int J Clin Exp Pathol. 2017 Aug 1;10(8):8709-8714. eCollection 2017.
2
Collagen's triglycine repeat number and phylogeny suggest an interdomain transfer event from a Devonian or Silurian organism into Trichodesmium erythraeum.胶原蛋白的三甘氨酸重复序列数量和系统发育表明,存在从泥盆纪或志留纪生物到红海束毛藻的结构域间转移事件。
J Mol Evol. 2008 Jun;66(6):539-54. doi: 10.1007/s00239-008-9111-7. Epub 2008 Jun 3.