Suppr超能文献

Mlsc的多基因控制

Multigene control of Mlsc.

作者信息

Click R E, Adelmann A

机构信息

Department of Surgery and Microbiology, University of Minnesota, Minneapolis 55455.

出版信息

Immunogenetics. 1988;28(6):412-6. doi: 10.1007/BF00355372.

Abstract

Festenstein originally described the Mls locus as a single dominant autosomal gene with four alleles which mapped in the 13th linkage group of chromosome 1. We subsequently presented evidence which indicated that the mixed leukocyte reaction stimulatory products of DBA/2 and CBA/J were controlled by two independently segregating Mls loci. Recently, Mlsd of CBA/J was shown to be composed of Mlsa of AKR and Mlsc of C3H. In the present report, classic segregation data is presented which indicates that Mlsc of C3H is controlled by three independently segregating loci. As defined by stimulatory patterns of numerous cell lines, we postulate the following: either one of the loci is shared with BALB.K, CE, C58, and partially with MA/MyJ, one is shared with CBA/H and CBA/J, and one is shared with BALB.K, CBA/J, and partially with CE; or the groups of shared determinants are controlled by different alleles of unique loci (or locus). In any event, Mlsc appears to be composed of at least three independently segregating loci; the number of alleles/locus is being investigated. In addition, C3H was stimulated by BALB.K (both were recently postulated to be Mlsc); this epitope was shared with CBA/J, CBA/H, AKR/Cum, Ma/MyJ, and C58/J.

摘要

费斯滕斯坦最初将Mls基因座描述为一个单一的显性常染色体基因,有四个等位基因,定位于1号染色体的第13个连锁群。我们随后提供的证据表明,DBA/2和CBA/J的混合淋巴细胞反应刺激产物受两个独立分离的Mls基因座控制。最近,CBA/J的Mlsd被证明由AKR的Mlsa和C3H的Mlsc组成。在本报告中,呈现了经典的分离数据,表明C3H的Mlsc受三个独立分离的基因座控制。根据众多细胞系的刺激模式定义,我们提出以下假设:要么其中一个基因座与BALB.K、CE、C58以及部分与MA/MyJ共享,一个与CBA/H和CBA/J共享,一个与BALB.K、CBA/J以及部分与CE共享;要么共享决定簇组由独特基因座(或基因座)的不同等位基因控制。无论如何,Mlsc似乎由至少三个独立分离的基因座组成;每个基因座的等位基因数量正在研究中。此外,C3H受到BALB.K的刺激(两者最近都被假定为Mlsc);这个表位与CBA/J、CBA/H、AKR/Cum、Ma/MyJ和C58/J共享。

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