MicroRNAs that target RGS۵

  • سال انتشار: 1394
  • محل انتشار: مجله علوم پایه پزشکی ایران، دوره: 18، شماره: 2
  • کد COI اختصاصی: JR_IJBMS-18-2_001
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 296
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نویسندگان

Amir Banaei-Esfahani

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran

Hamidreza Moazzeni

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran

Pooya Naseri Nosar

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran

Sadaf Amin

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran

Ehsan Arefian

School of Biology, College of Science, University of Tehran, Tehran, Iran

Masoud Soleimani

Stem Cell Technology Research Center, Tehran, Iran

Shahin Yazdani

Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Elahe Elahi

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran. School of Biology, College of Science, University of Tehran, Tehran, Iran

چکیده

Objective(s):An earlier meta-analysis on gene expression data derived from four microarray, two cDNA library, and one SAGE experiment had identified RGS۵ as one of only ten non-housekeeping genes that were reported to be expressed in human trabecular meshwork (TM) cells by all studies. RGS۵ encodes regulator of G-protein signaling-۵. The TM tissue is the route of aqueous fluid outflow, and is relevant to the pathology of glaucoma. MicroRNAs constitute the most recently identified components of the cellular machinery for gene regulation in eukaryotic cells. Given our long standing interest in glaucoma, we aimed to identify miRNAs that may target RGS۵. Materials and Methods: Eight miRNAs were selected for study using bioinformatics tools and available data on miRNAs expressed in the eye. Their effects were assessed using the dual luciferase assay.  ۳'-UTR segments of RGS۵ mRNA were cloned downstream of a luciferase coding gene in psiCHECK۲ vectors, and these were co-transfected with each of the miRNAs into HEK۲۹۳ cells. Results: The outcomes evidenced that one or more of the segments are in fact targeted by miR-۷, miR-۹, miR-۹۶, miR-۲۳a, miR-۲۳b, miR-۲۰۴, and miR-۲۱۱. Down regulations by the miRNAs were statistically significant. The effect of miR-۲۰۴ is considered particularly important as this miRNA is well known to regulate eye development and to affect multiple ocular functions. Conclusion: Our results justify further studies on regulation of RGS۵ expression and RGS۵ downstream functions by these miRNAs.

کلیدواژه ها

miR-۷, miR-۹, miR-۲۳a, miR-۲۳b, miR-۹۶, miR-۲۰۴, miR-۲۱۱, RGS۵

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