Nielsen J N, Hallenberg C, Frederiksen S, Sørensen P D, Lomholt B
Department of Medical Biochemistry and Genetics, Panum Institute, University of Copenhagen, Denmark.
Nucleic Acids Res. 1993 Aug 11;21(16):3631-6. doi: 10.1093/nar/21.16.3631.
Six human 5S rRNA genes and gene variants and one pseudogene have been sequenced. The six genes/variants were transcribed in a HeLa cell extract with about equal efficiency. Three genes contain the Sp1 binding sequence GGGCGG in position -43 to -38 and three genes contain the Sp1 like sequence GGGCCG in this position. The six genes contain furthermore one Sp1 binding site in a position about -245 and one ATF recognition site in a position about -202. A 12 bp sequence (GGCTCTTGGGGC) found in position -32 to -21 strongly influenced the transcriptional efficiency in vitro. This 12-mer, designated the D box, has also been found upstream a 5S rRNA gene from hamster and mouse. Removal of the Sp1 binding sites had no effect on the transcription in vitro whereas the transcriptional efficiency decreased to 10% if the D box was removed from the human 5S rRNA gene.
已对6个人类5S rRNA基因、基因变体及1个假基因进行了测序。这6个基因/变体在HeLa细胞提取物中的转录效率大致相同。3个基因在-43至-38位含有Sp1结合序列GGGCGG,另外3个基因在该位置含有类似Sp1的序列GGGCCG。这6个基因在约-245位还含有1个Sp1结合位点,在约-202位含有1个ATF识别位点。在-32至-21位发现的一个12 bp序列(GGCTCTTGGGGC)在体外对转录效率有强烈影响。这个12聚体,命名为D框,在仓鼠和小鼠的一个5S rRNA基因上游也有发现。去除Sp1结合位点对体外转录没有影响,而如果从人类5S rRNA基因中去除D框,转录效率则降至10%。