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一种新的免疫球蛋白基因命名法的建议。

A Proposed New Nomenclature for the Immunoglobulin Genes of .

机构信息

Division of B Cell Immunology, German Cancer Research Center, Heidelberg, Germany.

Immunology Division, The Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.

出版信息

Front Immunol. 2019 Dec 18;10:2961. doi: 10.3389/fimmu.2019.02961. eCollection 2019.

Abstract

Mammalian immunoglobulin (IG) genes are found in complex loci that contain hundreds of highly similar pseudogenes, functional genes and repetitive elements, which has made their investigation particularly challenging. High-throughput sequencing has provided new avenues for the investigation of these loci, and has recently been applied to study the IG genes of important inbred mouse strains, revealing unexpected differences between their IG loci. This demonstrated that the structural differences are of such magnitude that they call into question the merits of the current mouse IG gene nomenclatures. Three nomenclatures for the mouse IG heavy chain locus () are presently in use, and they are all positional nomenclatures using the C57BL/6 genome reference sequence as their template. The continued use of these nomenclatures requires that genes of other inbred strains be confidently identified as allelic variants of C57BL/6 genes, but this is clearly impossible. The unusual breeding histories of inbred mouse strains mean that, regardless of the genetics of wild mice, no single ancestral origin for the IG loci exists for laboratory mice. Here we present a general discussion of the challenges this presents for any IG nomenclature. Furthermore, we describe principles that could be followed in the formulation of a solution to these challenges. Finally, we propose a non-positional nomenclature that accords with the guidelines of the International Mouse Nomenclature Committee, and outline strategies that can be adopted to meet the nomenclature challenges if three systems are to give way to a new one.

摘要

哺乳动物免疫球蛋白(IG)基因位于复杂的基因座中,这些基因座包含数百个高度相似的假基因、功能基因和重复元件,这使得对它们的研究特别具有挑战性。高通量测序为这些基因座的研究提供了新的途径,最近已应用于研究重要近交系小鼠的 IG 基因,揭示了它们 IG 基因座之间出人意料的差异。这表明结构差异如此之大,以至于质疑当前的小鼠 IG 基因命名法的优点。目前有三种用于小鼠 IG 重链基因座()的命名法,它们都是使用 C57BL/6 基因组参考序列作为模板的位置命名法。继续使用这些命名法要求其他近交系的基因被确认为 C57BL/6 基因的等位基因变体,但这显然是不可能的。近交系小鼠的不寻常繁殖历史意味着,无论野生小鼠的遗传学如何,实验室小鼠的 IG 基因座都没有单一的祖先起源。在这里,我们对任何 IG 命名法都存在的这些挑战进行了一般性讨论。此外,我们描述了可以遵循的原则,以制定解决方案来应对这些挑战。最后,我们提出了一种非位置命名法,该命名法符合国际小鼠命名委员会的指导方针,并概述了如果要将三个系统改为新系统,可以采用的策略来应对命名法挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77e6/6930147/0c0e9f821cd2/fimmu-10-02961-g0001.jpg

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