Watanabe N, Ohshima Y
Institute of Biological Sciences, University of Tsukuba, Japan.
Eur J Biochem. 1988 May 16;174(1):125-32. doi: 10.1111/j.1432-1033.1988.tb14071.x.
There are about 50 copies of U1 RNA genes/pseudogenes in the rat genome. To date, we have isolated so far 25 phage clones carrying a U1 RNA gene/pseudogene from two rat genomic libraries. The 12 clones were selected by hybridization with the U1 RNA coding region under a stringent condition, and were mapped and sequenced. Here, we report three types of U1 RNA genes with different flanking sequences, all of which were shown to be induced to express in vivo by transfection with their polylinker-inserted maxi U1 RNA genes into cultured rat cells. Although these three classes of U1 RNA genes have few homologous flanking sequences, they provide both upstream and downstream of the genes two conserved blocks, which may possibly play an important role in U1 RNA expression.
大鼠基因组中约有50个U1 RNA基因/假基因拷贝。迄今为止,我们已从两个大鼠基因组文库中分离出25个携带U1 RNA基因/假基因的噬菌体克隆。通过在严格条件下与U1 RNA编码区杂交选择了12个克隆,并对其进行了定位和测序。在此,我们报告了三种具有不同侧翼序列的U1 RNA基因,通过将其多克隆位点插入的maxi U1 RNA基因转染到培养的大鼠细胞中,所有这些基因在体内均被诱导表达。尽管这三类U1 RNA基因的同源侧翼序列很少,但它们在基因的上游和下游均提供了两个保守区域,这可能在U1 RNA表达中起重要作用。