Luther Hans Peter
Medical Clinic I, Department of Cardiology, Humboldt University, Charité Hospital, Ziegelstrasse 5-9, 10117 Berlin, Germany.
J Mol Med (Berl). 2005 Jan;83(1):26-32. doi: 10.1007/s00109-004-0613-5. Epub 2004 Dec 9.
Endogenous antisense RNA has been detected for a range of eukaryotic genes and now appears to be a common phenomenon in mammalian cells. Its abundance compared to levels of its complementary sense mRNA indicates that antisense RNA may be involved in posttrancriptional regulation of a gene. In general a downregulating effect on gene expression has been demonstrated or suggested. Due to the heterogeneity in origin and character of different antisense transcripts alternative functions such as stabilizing the corresponding sense transcript and being part of gene recombination must be considered. Regulation by endogenous antisense RNA has been shown for a plethora of genes, including cardiac genes, such as myosin heavy chainMHC, atrial light chain, and troponin I. There is now growing evidence that antisense transcription is involved in human disease, and it is reasonable to consider antisense as a target for intervention procedures. Here we review the progress in our understanding of as well as the controversies arising from investigating the regulatory mechanisms of antisense RNA, with special focus on cardiac genes. Finally, links between antisense transcription and heart disease and the possible use of antisense as a target of cardiac intervention procedures are discussed.
已在一系列真核基因中检测到内源性反义RNA,目前它在哺乳动物细胞中似乎是一种常见现象。与互补的正义mRNA水平相比,其丰度表明反义RNA可能参与基因的转录后调控。一般来说,已证明或暗示其对基因表达具有下调作用。由于不同反义转录本的来源和性质存在异质性,必须考虑其替代功能,如稳定相应的正义转录本以及参与基因重组。已证明多种基因受内源性反义RNA调控,包括心脏基因,如肌球蛋白重链MHC、心房轻链和肌钙蛋白I。现在越来越多的证据表明反义转录与人类疾病有关,将反义作为干预措施的靶点是合理的。在此,我们综述了在理解反义RNA调控机制方面取得的进展以及由此引发的争议,特别关注心脏基因。最后,讨论了反义转录与心脏病之间的联系以及反义作为心脏干预措施靶点的可能用途。