Ariizumi K, Wang Z, Tucker P W
Department of Microbiology, University of Texas, Southwestern Medical Center, Dallas 75235.
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3695-9. doi: 10.1073/pnas.90.8.3695.
In several animal viruses, enhancers have been implicated in both DNA replication and transcriptional activation. The linkage of the two mechanisms appears intimate, in that common DNA binding factors can be shared. The immunoglobulin heavy chain (Igh) intronic [heavy chain joining region (JH)-mu chain constant region (C mu)] enhancer (E mu) is required for tissue-specific transcription of Igh genes and is essential for somatic recombination of diversity (D) and J segments. We show here that E mu is located at or near an origin of chromosomal DNA replication, which is more active in B lymphocytes than fibroblasts. E mu does not fulfill two criteria demonstrated for some cellular origins. E mu can initiate but not maintain autonomous replicating activity in B cells. E mu is unable to impart early replication timing to a transfected VDJ-C mu Igh locus in B cells. Instead we propose that E mu-associated ori activity contributes to tissue-specific Igh expression through local effects on chromatin structure leading to subsequent accessibility of transcription and/or recombination factors for the enhancer.
在几种动物病毒中,增强子与DNA复制和转录激活均有关联。这两种机制的联系似乎很紧密,因为可以共享共同的DNA结合因子。免疫球蛋白重链(Igh)内含子[重链连接区(JH)-μ链恒定区(Cμ)]增强子(Eμ)是Igh基因组织特异性转录所必需的,并且对于多样性(D)和J片段的体细胞重组至关重要。我们在此表明,Eμ位于染色体DNA复制起点处或其附近,该起点在B淋巴细胞中比在成纤维细胞中更活跃。Eμ不符合一些细胞起源所证明的两个标准。Eμ可以在B细胞中启动但不能维持自主复制活性。Eμ无法赋予转染到B细胞中的VDJ-Cμ Igh基因座早期复制时间。相反,我们提出,与Eμ相关的ori活性通过对染色质结构的局部影响导致增强子随后可被转录和/或重组因子接近,从而有助于组织特异性Igh表达。