Sequence analysis of the mouse RAG locus intergenic region.

F E Bertrand, S L Olson, D A Martin, G E Wu
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引用次数: 4

Abstract

The recombination activating genes RAG-1 and RAG-2 are highly conserved throughout evolution and are necessary and essential for the DNA rearrangement of antigen-receptor gene segments. These convergently transcribed genes are expressed primarily by developing B and T lineage cells. In addition, recent data suggest that the RAG locus can be reactivated in mouse germinal center B cells. Despite these well-defined patterns of expression, little is known about mechanism(s) regulating transcription of the RAG locus. Experiments with a mouse fibroblast line stably transfected with a genomic fragment of the RAG locus suggest that the intergenic region between RAG-1 and RAG-2 may contain information modulating RAG transcription. In order to begin testing this hypothesis, we have sequenced the 7.0-kb RAG intergenic region of the mouse. The sequence did not contain open reading frames larger than 60 amino acids. Analysis with GCG software identified several potential transcription-factor binding sequences within this region. Many of these are associated with transcriptional regulation of the Ig locus.

小鼠RAG基因座基因间区序列分析。
重组激活基因RAG-1和RAG-2在整个进化过程中高度保守,是抗原受体基因片段DNA重排的必要条件。这些趋同转录的基因主要通过发育中的B和T系细胞表达。此外,最近的数据表明,RAG位点可以在小鼠生发中心B细胞中被重新激活。尽管有这些明确的表达模式,但对RAG基因座调控转录的机制知之甚少。用稳定转染RAG基因片段的小鼠成纤维细胞系进行的实验表明,RAG-1和RAG-2之间的基因间区域可能含有调节RAG转录的信息。为了开始验证这一假设,我们对小鼠的7.0 kb的RAG基因间区进行了测序。该序列不包含超过60个氨基酸的开放阅读框。GCG软件分析鉴定出该区域内几个潜在的转录因子结合序列。其中许多与Ig位点的转录调控有关。
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