• 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

编码水貂免疫球蛋白λ链的cDNA克隆。

cDNA clones encoding mink immunoglobulin lambda chains.

作者信息

Najakshin A M, Belousov J S, Bogachev S S, Taranin A V

机构信息

Institute of Cytology and Genetics, Novosibirsk, Russia.

出版信息

Mol Immunol. 1993 Sep;30(13):1205-12. doi: 10.1016/0161-5890(93)90139-3.

DOI:10.1016/0161-5890(93)90139-3
PMID:8105375
Abstract

Screening of a mink cDNA library with an antibody probe resulted in the isolation of clone pIGL-2 containing an Ig lambda chain coding sequence. The sequence comprised almost the entire V segment as well as J, C, and 3'-untranslated sequences. A second clone, pIGL-10, was isolated by rescreening the cDNA library with the use of pIGL-2 as a probe. pIGL-10 was found to contain a frameshift deletion of a single nucleotide in the C region. pIGL-2 and pIGL-10 were 81% homologous to each other in the FR3 of the V segment, and 95% of homology was found in their C regions. The J segments of the two clones differed in only one nucleotide position. Comparison of cloned lambda chain sequences with those of other mammals revealed that mink V lambda and C lambda genes have the highest homology with their human counterparts. The V lambda sequence of clone pIGL-2 appears to be a homologue of human subgroup III V lambda genes. Southern blot hybridization of mink DNA with the C lambda and V lambda probes derived from pIGL-2 revealed five or six hybridizing C lambda fragments and at least 11 hybridizing V lambda fragments. This suggested that the lambda genes in carnivores, like those in primates, have duplicated extensively during evolution.

摘要

用抗体探针筛选水貂cDNA文库,分离出包含Igλ链编码序列的克隆pIGL - 2。该序列几乎包含整个V区段以及J、C和3'非翻译序列。通过用pIGL - 2作为探针重新筛选cDNA文库,分离出第二个克隆pIGL - 10。发现pIGL - 10在C区域存在一个单核苷酸的移码缺失。pIGL - 2和pIGL - 10在V区段的FR3中彼此同源性为81%,在其C区域发现95%的同源性。两个克隆的J区段仅在一个核苷酸位置上不同。将克隆的λ链序列与其他哺乳动物的序列进行比较,发现水貂Vλ和Cλ基因与其人类对应基因具有最高的同源性。克隆pIGL - 2的Vλ序列似乎是人类III亚组Vλ基因的同源物。用水貂DNA与源自pIGL - 2的Cλ和Vλ探针进行Southern印迹杂交,显示出五六个杂交的Cλ片段和至少11个杂交的Vλ片段。这表明食肉动物中的λ基因,与灵长类动物中的一样,在进化过程中已经广泛复制。

相似文献

1
cDNA clones encoding mink immunoglobulin lambda chains.编码水貂免疫球蛋白λ链的cDNA克隆。
Mol Immunol. 1993 Sep;30(13):1205-12. doi: 10.1016/0161-5890(93)90139-3.
2
[Cloning and sequencing of immunoglobin lambda-chain cDNA in american mink (Mustela vison].美洲水貂(鼬属水貂)免疫球蛋白λ链cDNA的克隆与测序
Genetika. 1990 Aug;26(8):1527-31.
3
Expression of immunoglobulin kappa and lambda chains in mink.水貂中免疫球蛋白κ链和λ链的表达
Eur J Immunol. 1993 Aug;23(8):1929-34. doi: 10.1002/eji.1830230830.
4
Genes encoding Xenopus laevis Ig L chains. Implications for the evolution of kappa and lambda chains.编码非洲爪蟾免疫球蛋白轻链的基因。对κ链和λ链进化的启示。
J Immunol. 1992 Dec 15;149(12):3968-77.
5
The mink gene for the lambda light immunoglobulin chain: characterization of cDNA and chromosomal localization.λ轻链免疫球蛋白的水貂基因:cDNA 特性及染色体定位
Mamm Genome. 1992;2(2):96-9. doi: 10.1007/BF00353856.
6
Structure of mink immunoglobulin gamma chain cDNA.
Dev Comp Immunol. 1996 Jul-Aug;20(4):231-40. doi: 10.1016/0145-305x(96)00019-5.
7
L chain isotype regulation in horse. I. Characterization of Ig lambda genes.马的轻链同种型调控。I. Igλ基因的特征
J Immunol. 1992 Dec 15;149(12):3927-36.
8
Heavy chain genes of rabbit IgG: isolation of a cDNA encoding gamma heavy chain and identification of two genomic C gamma genes.兔IgG重链基因:编码γ重链的cDNA的分离及两个基因组Cγ基因的鉴定
Proc Natl Acad Sci U S A. 1982 Oct;79(19):6018-22. doi: 10.1073/pnas.79.19.6018.
9
Molecular cloning of a bovine immunoglobulin lambda chain cDNA.牛免疫球蛋白λ链cDNA的分子克隆
Gene. 1988 Jul 15;67(1):41-8. doi: 10.1016/0378-1119(88)90006-6.
10
cDNA clones encoding immunoglobulin lambda chains from rabbit expressing the phenotype c7.编码来自表达c7表型兔子的免疫球蛋白λ链的cDNA克隆。
Eur J Immunol. 1990 Dec;20(12):2707-12. doi: 10.1002/eji.1830201227.