• 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

片段化免疫球蛋白基因与重链缺失突变体之间的相关性。

Correlation between fragmented immunoglobulin genes and heavy chain deletion mutants.

作者信息

Frangione B, Franklin E C

出版信息

Nature. 1979 Oct 18;281(5732):600-2. doi: 10.1038/281600a0.

DOI:10.1038/281600a0
PMID:114864
Abstract

It is generally accepted that the variable (V) and constant (C) regions of immunoglobulin (Ig) chains are under separate genetic control. The notion that the different domains and interdomain regions are also under the control of independent genetic units was initially based on the clearcut results obtained by studying the primary structure of deletion mutants and received definitive support from direct analysis of cloned heavy (H) and light (L) chain genes. Here we present additional studies carried out on two selected gamma 3 deletion mutants which indicate the genetic control of human H chains may be even more complex than previously believed.

摘要

人们普遍认为,免疫球蛋白(Ig)链的可变(V)区和恒定(C)区受不同的基因控制。不同结构域和结构域间区域也受独立遗传单位控制这一观点,最初是基于对缺失突变体一级结构研究所得出的明确结果,并从对克隆的重(H)链和轻(L)链基因的直接分析中得到了确凿支持。在此,我们展示了对两个选定的γ3缺失突变体进行的额外研究,这些研究表明人类H链的基因控制可能比之前认为的更为复杂。

相似文献

1
Correlation between fragmented immunoglobulin genes and heavy chain deletion mutants.片段化免疫球蛋白基因与重链缺失突变体之间的相关性。
Nature. 1979 Oct 18;281(5732):600-2. doi: 10.1038/281600a0.
2
An immunoglobulin deletion mutant with implications for the heavy-chain switch and RNA splicing.一种对重链转换和RNA剪接有影响的免疫球蛋白缺失突变体。
Nature. 1980 Aug 14;286(5774):669-75. doi: 10.1038/286669a0.
3
Human heavy chain disease protein WIS: implications for the organization of immunoglobulin genes.人类重链病蛋白WIS:对免疫球蛋白基因组织的影响
Proc Natl Acad Sci U S A. 1979 Jan;76(1):452-6. doi: 10.1073/pnas.76.1.452.
4
Gene mutations and alternate RNA splicing result in truncated Ig L chains in human gamma H chain disease.基因突变和替代性RNA剪接导致人类γ重链病中截短的Ig轻链。
J Immunol. 1988 Sep 1;141(5):1738-44.
5
Multiple genomic defects result in an alternative RNA splice creating a human gamma H chain disease protein.多种基因组缺陷导致一种替代RNA剪接,产生一种人类γ重链病蛋白。
J Immunol. 1988 Sep 1;141(5):1762-8.
6
gamma Heavy chain disease in man: cDNA sequence supports partial gene deletion model.人类γ重链病:cDNA序列支持部分基因缺失模型。
Proc Natl Acad Sci U S A. 1982 May;79(10):3260-4. doi: 10.1073/pnas.79.10.3260.
7
Articular, monoclonal gamma3 heavy-chain deposition disease: characterization of a partially deleted heavy-chain gene and its protein product synthesized in vivo and in vitro.关节型单克隆γ3重链沉积病:体内外合成的部分缺失重链基因及其蛋白产物的特征
Arthritis Rheum. 2003 Nov;48(11):3266-71. doi: 10.1002/art.11298.
8
Unusual genes at the aminoterminus of human immunoglobulin variants.人类免疫球蛋白变体氨基末端的异常基因。
Nature. 1978 Jun 1;273(5661):400-1. doi: 10.1038/273400a0.
9
Primary structure of human gamma 3 immunoglobulin deletion mutant: gamma 3 heavy-chain disease protein Wis.人γ3免疫球蛋白缺失突变体的一级结构:γ3重链病蛋白Wis
Biochemistry. 1980 Sep 2;19(18):4304-8. doi: 10.1021/bi00559a024.
10
Sequence of the cloned gene for the constant region of murine gamma 2b immunoglobulin heavy chain.小鼠γ2b免疫球蛋白重链恒定区克隆基因的序列
Science. 1979 Dec 14;206(4424):1303-6. doi: 10.1126/science.117549.

引用本文的文献

1
IgA proteases of two distinct specificities are released by Neisseria meningitidis.脑膜炎奈瑟菌可释放出两种具有不同特异性的IgA蛋白酶。
J Exp Med. 1980 Nov 1;152(5):1442-7. doi: 10.1084/jem.152.5.1442.
2
J segment in human delta chains.人类δ链中的J片段。
Immunology. 1980 Aug;40(4):657-64.
3
Gamma heavy chain disease in man. Genomic sequence reveals two noncontiguous deletions in a single gene.人类γ重链病。基因组序列揭示单个基因中的两个非连续缺失。
J Clin Invest. 1988 Oct;82(4):1244-52. doi: 10.1172/JCI113722.