Aguilera R J, Hope T J, Sakano H
EMBO J. 1985 Dec 30;4(13B):3689-93. doi: 10.1002/j.1460-2075.1985.tb04136.x.
We have analyzed enhancer deletions found in murine plasmacytomas by DNA cloning. This analysis revealed that the deletions occurred between the JH region and the switch region, removing the Ig heavy chain enhancer. The loss of the enhancer did not significantly affect the level of heavy chain expression as determined by RNA blots. Nucleotide sequence analysis revealed that there are no characteristic or homologous sequences around the recombination site. Extra nucleotides were found at the recombination sites, in a manner analogous to Ig and T-cell receptor V-D-J joining. The germline JH and switch sequences involved in the deletion were analyzed by the in vitro DNA cleavage system with an endonucleolytic activity purified from mouse fetal liver nuclear extracts. It was found that the germline JH DNA was strongly cleaved at the deletion recombination site.
我们通过DNA克隆分析了在鼠浆细胞瘤中发现的增强子缺失情况。该分析表明,缺失发生在JH区域和转换区域之间,移除了Ig重链增强子。如RNA印迹分析所示,增强子的缺失并未显著影响重链表达水平。核苷酸序列分析显示,重组位点周围没有特征性或同源序列。在重组位点发现了额外的核苷酸,其方式类似于Ig和T细胞受体V-D-J连接。通过从鼠胎儿肝核提取物中纯化的具有内切核酸酶活性的体外DNA切割系统,分析了参与缺失的种系JH和转换序列。结果发现,种系JH DNA在缺失重组位点被强烈切割。