Manser T, Gesteland R F
Cell. 1982 May;29(1):257-64. doi: 10.1016/0092-8674(82)90110-6.
We have cloned and sequenced several distinct loci from the human genome whose sequences agree exactly and are colinear with the sequence of the small nuclear RNA U1. There appear to be 100-150 such U1 loci in the human genome. Although these loci are not in close clusters or in small tandem repeats in the genome, the majority of them have remarkably similar genomic environments. Several potential RNA polymerase termination sites exist in the immediate 3' flanking regions of the loci studied; however, no TATA box is found in the immediate 5' flanking sequences. These observations, with the findings of others concerning the transcription of U1, suggest that U1 RNA is synthesized from a family of transcription units. These data are consistent with the proposal that RNA polymerase II may synthesize primary transcripts from these transcription units, which are processed at both the 5' and 3' ends to yield mature U1 RNA and possibly other RNA species of unknown function.
我们已经从人类基因组中克隆并测序了几个不同的基因座,其序列与小核RNA U1的序列完全一致且呈共线性。人类基因组中似乎有100 - 150个这样的U1基因座。尽管这些基因座在基因组中并非紧密成簇或形成小的串联重复序列,但它们中的大多数具有非常相似的基因组环境。在所研究基因座的紧邻3'侧翼区域存在几个潜在的RNA聚合酶终止位点;然而,在紧邻的5'侧翼序列中未发现TATA框。这些观察结果,连同其他人关于U1转录的发现,表明U1 RNA是由一族转录单位合成的。这些数据与RNA聚合酶II可能从这些转录单位合成初级转录本的提议一致,这些初级转录本在5'和3'末端都经过加工以产生成熟的U1 RNA以及可能其他功能未知的RNA种类。