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Journal ArticleDOI

The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a

Sonia Guil, +1 more
- 10 Jun 2007 - 
- Vol. 14, Iss: 7, pp 591-596
TLDR
It is shown that hnRNP A1 binds specifically to the primary RNA sequence pri-miR-18a before Drosha processing, which underscores a previously uncharacterized role for general RNA-binding proteins as auxiliary factors that facilitate the processing of specific miRNAs.
Abstract
hnRNP A1 is an RNA-binding protein involved in various aspects of RNA processing. Use of an in vivo cross-linking and immunoprecipitation protocol to find hnRNP A1 RNA targets resulted in the identification of a microRNA (miRNA) precursor, pre-miR-18a. This microRNA is expressed as part of a cluster of intronic RNAs, including miR-17, miR-18a, miR-19a, miR-20a, miR-19b-1 and miR-92, and potentially acts as an oncogene. Here we show that hnRNP A1 binds specifically to the primary RNA sequence pri-miR-18a before Drosha processing. HeLa cells depleted of hnRNP A1 have reduced in vitro processing activity with pri-miR-18a and also show reduced abundances of endogenous pre-miR-18a. Furthermore, we show that hnRNP A1 is required for miR-18a–mediated repression of a target reporter in vivo. These results underscore a previously uncharacterized role for general RNA-binding proteins as auxiliary factors that facilitate the processing of specific miRNAs.

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Citations
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Journal ArticleDOI

Regulation of microRNA biogenesis

TL;DR: Small non-coding RNAs that function as guide molecules in RNA silencing are involved in nearly all developmental and pathological processes in animals and their dysregulation is associated with many human diseases.
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Biogenesis of small RNAs in animals.

TL;DR: This Review summarizes the current knowledge of how these intriguing molecules are generated in animal cells.
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Transcriptome-wide Identification of RNA-Binding Protein and MicroRNA Target Sites by PAR-CLIP

TL;DR: This study developed a cell-based crosslinking approach to determine at high resolution and transcriptome-wide the binding sites of cellular RBPs and miRNPs and revealed that these factors bind thousands of sites containing defined sequence motifs and have distinct preferences for exonic versus intronic or coding versus untranslated transcript regions.
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Many roads to maturity: microRNA biogenesis pathways and their regulation

TL;DR: Recent advances in knowledge of the microRNA biosynthesis pathways are reviewed and their impact on post-transcriptional microRNA regulation during tumour development is discussed.
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MicroRNA biogenesis pathways in cancer

TL;DR: Global miRNA depletion caused by genetic and epigenetic alterations in components of the miRNA biogenesis machinery is oncogenic, highlighting the importance of miRNA dysregulation in cancer.
References
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Journal ArticleDOI

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TL;DR: Evidence is mounting that animal miRNAs are more numerous, and their regulatory impact more pervasive, than was previously suspected.
Journal ArticleDOI

Identification of novel genes coding for small expressed RNAs.

TL;DR: It is shown that many 21- and 22-nt expressed RNAs, termed microRNAs, exist in invertebrates and vertebrates and that some of these novel RNAs are highly conserved, which suggests that sequence-specific, posttranscriptional regulatory mechanisms mediated by smallRNAs are more general than previously appreciated.
Journal ArticleDOI

A microRNA polycistron as a potential human oncogene

TL;DR: It is found that the levels of the primary or mature microRNAs derived from the mir-17–92 locus are often substantially increased in human B-cell lymphomas, and the cluster is implicate as a potential human oncogene.
Journal ArticleDOI

Nuclear Export of MicroRNA Precursors

TL;DR: Exposure of Exportin-5 (Exp5) mediates efficient nuclear export of short miRNA precursors (pre-miRNAs) and its depletion by RNA interference results in reduced miRNA levels.
Journal ArticleDOI

MicroRNA maturation: stepwise processing and subcellular localization.

TL;DR: In vivo and in vitro evidence is presented that these clustered miRNAs are expressed polycistronically and are processed through at least two sequential steps, including the two processing steps and the nuclear export step, suggesting that the regulation of miRNA expression may occur at multiple levels.
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