Gil I, Gallego M E, Renart J, Cruces J
Nucleic Acids Res. 1987 Aug 11;15(15):6007-16. doi: 10.1093/nar/15.15.6007.
The proximal part of the Intergenic Spacer, as well as most of the External Transcribed Spacer of the ribosomal RNA type I genes from the crustacean Artemia have been sequenced. We have identified in the Intergenic Spacer five repeats of around 600 bp in length and, possibly, two imperfect or truncated repeats, derived from the principal ones. These sequences are separated by 485 bp from the 17S rRNA coding sequence. We have also identified the start point of transcription by S1 nuclease analysis. This start point is found 248 bp inside the first repeat. The sequence around the start point shows homology with that described for other members of the same phylum, mostly insects. The most conserved regions are from -1 to +25, and the G residue at position -16. At least the three 600-bp repeats upstream from that containing the promoter also contain the start point sequence, and could therefore act as initiation sites for snPIRNA and/or as enhancer sequences for ribosomal RNA gene transcription.
对甲壳动物卤虫核糖体RNA I型基因的基因间隔区近端部分以及大部分外部转录间隔区进行了测序。我们在基因间隔区中鉴定出了五个长度约为600 bp的重复序列,以及可能源自主要重复序列的两个不完美或截断的重复序列。这些序列与17S rRNA编码序列相隔485 bp。我们还通过S1核酸酶分析确定了转录起始点。该起始点位于第一个重复序列内部248 bp处。起始点周围的序列与同一门的其他成员(主要是昆虫)所描述的序列具有同源性。最保守的区域是从-1到+25,以及-16位的G残基。至少在包含启动子的那个重复序列上游的三个600 bp重复序列也包含起始点序列,因此可以作为snPIRNA的起始位点和/或核糖体RNA基因转录的增强子序列。