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转基因小鼠中IgH基因座3'增强子对ε种系转录和转换区突变的调控。

Regulation of epsilon germline transcription and switch region mutations by IgH locus 3' enhancers in transgenic mice.

作者信息

Laurencikiene Jurga, Tamosiunas Vytas, Severinson Eva

机构信息

Department of Cell and Molecular Biology, Karolinska Institutet, SE-17177 Stockholm, Sweden.

出版信息

Blood. 2007 Jan 1;109(1):159-67. doi: 10.1182/blood-2006-02-005355. Epub 2006 Sep 12.

DOI:10.1182/blood-2006-02-005355
PMID:16968901
Abstract

Germline (GL) transcription is regulated by specific promoters and immunoglobulin heavy chain (IgH) 3' locus enhancers and is necessary for Ig class-switch recombination (CSR). We have generated different transgenic lines containing the GL epsilon promoter, switch (S) epsilon region, and constant (C) epsilon region with or without the DNase I-sensitive regions (HS) 3A-HS1,2 or HS3B-HS4 3' IgH enhancer pairs. The enhancerless construct was expressed in B cells activated by interleukin (IL)-4 and CD40, thus resembling regulation of the endogenous gene. Both enhancer-containing transgenes efficiently increased expression in B cells and were strongly up-regulated by stimuli. In addition, Sepsilon regions of the transgene containing HS3B-HS4 were mutated in activated, sorted B cells. Such mutations are known to precede CSR and are dependent on activation-induced cytidine deaminase (AID). Our findings show that all elements necessary for recruitment of the recombination machinery are present in the transgene containing HS3 and HS4. These enhancers probably provide something more specific than mere increased accessibility of switch regions. We propose that transcription factors binding the enhancers help to target the recombination machinery to the switch regions.

摘要

种系(GL)转录受特定启动子和免疫球蛋白重链(IgH)3'基因座增强子调控,是Ig类别转换重组(CSR)所必需的。我们构建了不同的转基因品系,包含GL ε启动子、转换(S)ε区域和恒定(C)ε区域,有或没有DNA酶I敏感区域(HS)3A - HS1,2或HS3B - HS4 3'Igh增强子对。无增强子构建体在由白细胞介素(IL)-4和CD40激活的B细胞中表达,因此类似于内源基因的调控。两种含增强子的转基因均能有效增加B细胞中的表达,并被刺激强烈上调。此外,含有HS3B - HS4的转基因的Sε区域在活化的分选B细胞中发生了突变。已知此类突变先于CSR发生,且依赖于激活诱导的胞苷脱氨酶(AID)。我们的研究结果表明,重组机制募集所需的所有元件都存在于含有HS3和HS4的转基因中。这些增强子可能提供的不仅仅是开关区域可及性的单纯增加。我们提出,结合增强子的转录因子有助于将重组机制靶向到开关区域。

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