Mattaj I W, Zeller R
EMBO J. 1983;2(11):1883-91. doi: 10.1002/j.1460-2075.1983.tb01675.x.
Xenopus laevis U2 small nuclear RNA (snRNA) genes were isolated and expressed by microinjection into frog oocytes. The genes are organised in short tandemly repeated units of approximately 830 bp. Some of the cloned tandem repeats are closely linked to genes coding for U5 snRNA, tRNA and an uncharacterised 7S RNA. No evidence was found for U2 snRNA pseudogenes. Single repeat units are transcriptionally active, showing that all the signals necessary for U2 snRNA transcription are included in an 831-bp segment of DNA. Sequence analysis of a cloned repeat unit showed that Xenopus and rat U2 snRNAs are 94% homologous. Flanking regions 5' and 3' to the coding sequence were found which shared extensive homology with similarly positioned sequences in human U1 snRNA genes. Part of the 3' non-coding region homology (consensus TTTNAAAGAAT) was found in many other genes transcribed by RNA polymerase II.
非洲爪蟾的U2小核RNA(snRNA)基因通过显微注射到蛙卵母细胞中进行分离和表达。这些基因以约830 bp的短串联重复单元形式组织。一些克隆的串联重复序列与编码U5 snRNA、tRNA和一种未鉴定的7S RNA的基因紧密相连。未发现U2 snRNA假基因的证据。单个重复单元具有转录活性,表明U2 snRNA转录所需的所有信号都包含在一段831 bp的DNA片段中。对一个克隆的重复单元进行序列分析表明,非洲爪蟾和大鼠的U2 snRNAs有94%的同源性。在编码序列的5'和3'侧翼区域发现了与人U1 snRNA基因中类似定位序列具有广泛同源性的序列。3'非编码区域的部分同源性(共有序列TTTNAAAGAAT)在许多其他由RNA聚合酶II转录的基因中也有发现。