miFAST: A novel and rapid microRNA target capture method

Ashley M. Poenitzsch Strong; Scott M. Berry; David J. Beebe; Jian Liang Li; Vladimir Spiegelman

doi:10.1002/mc.22780

miFAST: A novel and rapid microRNA target capture method

Ashley M. Poenitzsch Strong, Scott M. Berry, David J. Beebe, Jian Liang Li, Vladimir Spiegelman

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

MicroRNAs (miRNAs), small 22-25 nucleotide non-coding RNAs, play important roles in cellular and tumor biology. However, characterizing miRNA function remains challenging due to an abundance of predicted targets and an experimental bottleneck in identifying biologically relevant direct targets. Here, we developed a novel technique (miFAST) to identify direct miRNA target genes. Using miFAST, we confirmed several previously reported miR-340 target genes and identified five additional novel direct miR-340 targets in melanoma cells. This methodology can also be efficiently applied for the global characterization of miRNA targets. Utilizing miFAST to characterize direct miRNA targetomes will further our understanding of miRNA biology and function.

Original language	English (US)
Pages (from-to)	559-566
Number of pages	8
Journal	Molecular Carcinogenesis
Volume	57
Issue number	4
DOIs	https://doi.org/10.1002/mc.22780
State	Published - Apr 2018

All Science Journal Classification (ASJC) codes

Molecular Biology
Cancer Research

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10.1002/mc.22780

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title = "miFAST: A novel and rapid microRNA target capture method",

abstract = "MicroRNAs (miRNAs), small 22-25 nucleotide non-coding RNAs, play important roles in cellular and tumor biology. However, characterizing miRNA function remains challenging due to an abundance of predicted targets and an experimental bottleneck in identifying biologically relevant direct targets. Here, we developed a novel technique (miFAST) to identify direct miRNA target genes. Using miFAST, we confirmed several previously reported miR-340 target genes and identified five additional novel direct miR-340 targets in melanoma cells. This methodology can also be efficiently applied for the global characterization of miRNA targets. Utilizing miFAST to characterize direct miRNA targetomes will further our understanding of miRNA biology and function.",

author = "{Poenitzsch Strong}, {Ashley M.} and Berry, {Scott M.} and Beebe, {David J.} and Li, {Jian Liang} and Vladimir Spiegelman",

note = "Publisher Copyright: {\textcopyright} 2018 Wiley Periodicals, Inc.",

year = "2018",

month = apr,

doi = "10.1002/mc.22780",

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T2 - A novel and rapid microRNA target capture method

AU - Poenitzsch Strong, Ashley M.

AU - Berry, Scott M.

AU - Beebe, David J.

AU - Li, Jian Liang

AU - Spiegelman, Vladimir

PY - 2018/4

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AB - MicroRNAs (miRNAs), small 22-25 nucleotide non-coding RNAs, play important roles in cellular and tumor biology. However, characterizing miRNA function remains challenging due to an abundance of predicted targets and an experimental bottleneck in identifying biologically relevant direct targets. Here, we developed a novel technique (miFAST) to identify direct miRNA target genes. Using miFAST, we confirmed several previously reported miR-340 target genes and identified five additional novel direct miR-340 targets in melanoma cells. This methodology can also be efficiently applied for the global characterization of miRNA targets. Utilizing miFAST to characterize direct miRNA targetomes will further our understanding of miRNA biology and function.

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JO - Molecular Carcinogenesis

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miFAST: A novel and rapid microRNA target capture method

Abstract

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