Johansen Steinar D, Vader Anna, Sjøttem Eva, Nielsen Henrik
Department of Molecular Biotechnology, Institute of Medical Biology, University of Tromsø, Tromsø, Norway.
RNA Biol. 2006 Oct;3(4):157-62. doi: 10.4161/rna.3.4.3958. Epub 2006 Oct 5.
Two different isolates of the myxomycete Didymium iridis harbour homing endonuclease genes that are expressed from group I introns inserted into identical sites within the small subunit ribosomal DNA. The homing endonuclease proteins are related in sequence, and their gene structures share similar features such as the presence of small spliceosomal introns and functional polyadenylation sites. However, they are transcribed from opposite strands of the ribosomal DNA and presumable by different RNA polymerases. We have previously described the in vivo expression of the I-DirI homing endonuclease from within the ribosomal RNA precursor. In this paper, we demonstrate the in vivo expression of the I-DirII homing endonuclease from the opposite strand of the Didymium rRNA gene. A comparison of the expression strategies of the two genes demonstrates the feasibility of antisense expression and provides insight into nucleolar gene expression.
黏菌双盘菌的两种不同分离株含有归巢内切核酸酶基因,这些基因由插入小亚基核糖体DNA相同位点的I组内含子表达。归巢内切核酸酶蛋白在序列上相关,并且它们的基因结构具有相似特征,例如存在小剪接体内含子和功能性聚腺苷酸化位点。然而,它们从核糖体DNA的相反链转录,推测由不同的RNA聚合酶转录。我们之前描述了核糖体RNA前体内I-DirI归巢内切核酸酶的体内表达。在本文中,我们展示了双盘菌rRNA基因相反链上I-DirII归巢内切核酸酶的体内表达。对这两个基因表达策略的比较证明了反义表达的可行性,并为核仁基因表达提供了见解。