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免疫球蛋白重链基因座受体编辑所涉及的分子机制。

Molecular mechanisms involved in receptor editing at the Ig heavy chain locus.

作者信息

Fanning L, Bertrand F E, Steinberg C, Wu G E

机构信息

Department of Immunology and Wellesley Hospital Research Institute, University of Toronto, Ontario, Canada.

出版信息

Int Immunol. 1998 Feb;10(2):241-6. doi: 10.1093/intimm/10.2.241.

Abstract

In receptor editing, a phenomenon that has recently come to light and into favor, a rearranged VDJ or VJ gene segment encoding a variable region of an Ig chain is replaced by another. In this commentary, the molecular mechanisms involved in the editing process are examined in some detail. Editing is most likely mediated by the same V(D)J recombinase activity responsible for the formation of the original VDJ or VJ segment. An embedded heptamer, which is present near the 3' end of many VH elements, is used as the recombination signal sequence at the Ig heavy chain locus. It has been postulated that the mediation of receptor editing is the evolutionary force maintaining the embedded heptamer. Some of the evidence for and against this hypothesis is discussed.

摘要

在受体编辑(一种最近才被发现并受到青睐的现象)中,编码Ig链可变区的重排VDJ或VJ基因片段会被另一个所取代。在这篇评论中,将对编辑过程中涉及的分子机制进行较为详细的研究。编辑很可能是由负责原始VDJ或VJ片段形成的相同V(D)J重组酶活性介导的。许多VH元件3'端附近存在的一个嵌入七聚体,被用作Ig重链基因座处的重组信号序列。据推测,受体编辑的介导作用是维持该嵌入七聚体的进化力量。本文将讨论支持和反对这一假说的一些证据。

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