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Deletion of human JK segments by site-specific recombination recognizing the conserved nonamer and heptamer sequences.

机译:通过识别保守的九聚体和七聚体序列的位点特异性重组删除人JK节段。

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摘要

Mapping and partial sequencing of the productive K chain genomic DNA of FK-001 demonstrated a 1.8-kb deletion including the JK2, JK3, JK4, and JK5 segments. This deletion occurred between the heptamer recombination signal sequence of the JK2 segment and the heptamer-like sequence located 1.8 kb downstream of the JK2 segment. The recombination reaction kept the reciprocally joined signal sequences on the chromosome and deleted the intervening DNA segment. The cloned FK-001 K chain gene was expressed efficiently in mouse myeloma cells, demonstrating that the 1.8-kb deleted region conferred no functions for gene expression.
机译:FK-001的生产性K链基因组DNA的作图和部分测序证明包括JK2,JK3,JK4和JK5区段的1.8kb缺失。该缺失发生在JK2区段的七聚体重组信号序列和位于JK2区段下游1.8kb的七聚体样序列之间。重组反应将相互连接的信号序列保留在染色体上,并删除了插入的DNA片段。克隆的FK-001 K链基因在小鼠骨髓瘤细胞中有效表达,表明1.8kb缺失区不赋予基因表达功能。

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