期刊
MOLECULAR BIOTECHNOLOGY
卷 38, 期 3, 页码 257-268出版社
HUMANA PRESS INC
DOI: 10.1007/s12033-007-9013-8
关键词
small RNA; non-coding RNAs; siRNA; miRNA; intronic miRNA; transposons; biogenesis; mechanism; identification; targeting; fine-tuning; gene function; gene therapy; anti-viral vaccine; drug development; future directions
资金
- NCI NIH HHS [R01 CA085722, CA 85722] Funding Source: Medline
MicroRNAs (miRNAs), widely distributed, small regulatory RNA genes, target both messenger RNA (mRNA) degradation and suppression of protein translation based on sequence complementarity between the miRNA and its targeted mRNA. Different names have been used to describe various types of miRNA. During evolution, RNA retroviruses or transgenes invaded the eukaryotic genome and inserted in the non-coding regions of DNA, conceivably acting as transposon-like jumping genes, providing defense from viral invasion and fine-funing of gene expression as a secondary level of gene modulation in eukaryotes. When a transposon is inserted in the intron, it becomes an intronic miRNA, taking advantage of the protein synthesis machinery, i.e., mRNA transcription and splicing, as a means for processing and maturation. Recently, miRNAs have been found to play an important, but not life-threatening, role in embryonic development. They might play a pivotal role in diverse biological systems in various organisms, facilitating a quick response and accurate plotting of body physiology and structures. Based on these unique properties, man-made intronic miRNAs have been developed for in vitro evaluation of gene function, in vivo gene therapy and generation of transgenic animal models. The biogenesis and identification of miRNAs, potential applications, and future directions for research are presented, hopefully providing a guideline for further miRNA and gene function studies.
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