Tomecki Rafal, Dmochowska Aleksandra, Gewartowski Kamil, Dziembowski Andrzej, Stepien Piotr P
Department of Genetics, Warsaw University, Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland.
Nucleic Acids Res. 2004 Nov 16;32(20):6001-14. doi: 10.1093/nar/gkh923. Print 2004.
We report here on the identification of a novel human nuclear-encoded mitochondrial poly(A) polymerase. Immunocytochemical experiments confirm that the enzyme indeed localizes to mitochondrial compartment. Inhibition of expression of the enzyme by RNA interference results in significant shortening of the poly(A) tails of the mitochondrial ND3, COX III and ATP 6/8 transcripts, suggesting that the investigated protein represents a bona fide mitochondrial poly(A) polymerase. This is in agreement with our sequencing data which show that poly(A) tails of several mitochondrial messengers are composed almost exclusively of adenosine residues. Moreover, the data presented here indicate that all analyzed mitochondrial transcripts with profoundly shortened poly(A) tails are relatively stable, which in turn argues against the direct role of long poly(A) extensions in the stabilization of human mitochondrial messengers.
我们在此报告一种新型人类核编码线粒体聚腺苷酸聚合酶的鉴定。免疫细胞化学实验证实该酶确实定位于线粒体区室。通过RNA干扰抑制该酶的表达会导致线粒体ND3、COX III和ATP 6/8转录本的聚腺苷酸尾显著缩短,这表明所研究的蛋白质代表一种真正的线粒体聚腺苷酸聚合酶。这与我们的测序数据一致,该数据显示几种线粒体信使RNA的聚腺苷酸尾几乎完全由腺苷残基组成。此外,此处呈现的数据表明,所有分析的聚腺苷酸尾大幅缩短的线粒体转录本相对稳定,这反过来又反驳了长聚腺苷酸延伸在人类线粒体信使RNA稳定中的直接作用。