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NeoR 基因取代 Imu-Cmu 内含子改变了 Imu 种系表达,但对 V(D)J 重组没有影响。

Replacement of Imu-Cmu intron by NeoR gene alters Imu germ-line expression but has no effect on V(D)J recombination.

机构信息

CNRS UMR 5089, Institut de Pharmacologie et de Biologie Structurale, Equipe Instabilité génétique et régulation transcriptionnelle, 205 route de Narbonne, 31077 Toulouse, France.

出版信息

Mol Immunol. 2010 Feb;47(5):961-71. doi: 10.1016/j.molimm.2009.11.024. Epub 2009 Dec 28.

Abstract

The NeoR gene has often been used to unravel the mechanisms underlying long-range interactions between promoters and enhancers during V(D)J assembly and class switch recombination (CSR) in the immunoglobulin heavy chain (IgH) locus. This approach led to the notion that CSR is regulated through competition of germ-line (GL) promoters for activities displayed by the 3' regulatory region (3'RR). This polarized long-range effect of the 3'RR is disturbed upon insertion of NeoR gene in the IgH constant (C(H)) region, where only GL transcription derived from upstream GL promoters is impaired. In the context of V(D)J recombination, replacement of Emu enhancer or Emu core enhancer (cEmu) by NeoR gene fully blocked V(D)J recombination and mu0 GL transcription which originates 5' of DQ52 and severely diminished Imu GL transcription derived from Emu/Imu promoter, suggesting a critical role for cEmu in the regulation of V(D)J recombination and of mu0 and Imu expression. Here we focus on the effect of NeoR gene on mu0 and Imu GL transcription in a mouse line in which the Imu-Cmu intron was replaced by a NeoR gene in the sense-orientation. B cell development was characterized by a marked but incomplete block at the pro-B cell stage. However, V(D)J recombination was unaffected in sorted pro-B and pre-B cells excluding an interference with the accessibility control function of Emu. mu0 GL transcription initiation was relatively normal but the maturation step seemed to be affected most likely through premature termination at NeoR polyadenylation sites. In contrast, Imu transcription initiation was impaired suggesting an interference of NeoR gene with the IgH enhancers that control Imu expression. Surprisingly, in stark contrast with the NeoR effect in the C(H) region, LPS-induced NeoR expression restored Imu transcript levels to normal. The data suggest that Emu enhancer may be the master control element that counteracts the down-regulatory "Neo effect" on Imu expression upon LPS stimulation. More importantly, they reveal a complex and developmentally regulated interplay between IgH enhancers in the control of Imu expression.

摘要

NeoR 基因常用于揭示 V(D)J 组装过程中启动子和增强子之间长距离相互作用的机制,以及免疫球蛋白重链 (IgH) 基因座中的类别转换重组 (CSR)。这种方法导致 CSR 通过生殖系 (GL) 启动子与 3' 调控区 (3'RR) 显示的活性竞争来调节的概念。3'RR 的这种极化长距离效应在 NeoR 基因插入 IgH 恒定区 (C(H)) 时受到干扰,其中只有来自上游 GL 启动子的 GL 转录受到损害。在 V(D)J 重组的情况下,用 NeoR 基因替换 Emu 增强子或 Emu 核心增强子 (cEmu) 完全阻断了 V(D)J 重组和源自 DQ52 5'的 mu0 GL 转录,并严重减少了源自 Emu/Imu 启动子的 Imu GL 转录,表明 cEmu 在 V(D)J 重组和 mu0 和 Imu 表达的调节中起着关键作用。在这里,我们关注 NeoR 基因对在 sense 取向中将 Imu-Cmu 内含子替换为 NeoR 基因的小鼠系中 mu0 和 Imu GL 转录的影响。B 细胞发育在 pro-B 细胞阶段表现出明显但不完全的阻断。然而,在分选的 pro-B 和 pre-B 细胞中,V(D)J 重组不受影响,排除了对 Emu 可及性控制功能的干扰。mu0 GL 转录起始相对正常,但成熟步骤似乎受到影响,最有可能是通过在 NeoR 多聚腺苷酸化位点过早终止。相比之下,Imu 转录起始受到损害,表明 NeoR 基因干扰了控制 Imu 表达的 IgH 增强子。令人惊讶的是,与 NeoR 在 C(H) 区域的作用形成鲜明对比的是,LPS 诱导的 NeoR 表达将 Imu 转录本水平恢复到正常水平。数据表明,Emu 增强子可能是主控制元件,可在 LPS 刺激时抵消对 Imu 表达的下调“Neo 效应”。更重要的是,它们揭示了 IgH 增强子在控制 Imu 表达中的复杂和发育调节相互作用。

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