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Antagonistic role of hnRNP A1 and KSRP in the regulation of let-7a biogenesis

Authors: Michlewski, Gracjan; Cáceres, Javier F.;

Antagonistic role of hnRNP A1 and KSRP in the regulation of let-7a biogenesis

Abstract

The pluripotency-promoting proteins Lin28a and Lin28b act as post-transcriptional repressors of let-7 miRNA biogenesis in undifferentiated embryonic stem cells. The levels of mature let-7a differ substantially in cells lacking Lin28 expression, indicating the existence of additional mechanism(s) of post-transcriptional regulation. Here, we present evidence supporting a role for heteronuclear ribonucleoprotein A1 (hnRNP A1) as a negative regulator of let-7a. HnRNP A1 binds the conserved terminal loop of pri-let-7a-1 and inhibits its processing by Drosha. Levels of mature let-7a negatively correlate with hnRNP A1 levels in somatic cell lines. Furthermore, hnRNP A1 depletion increased pri-let-7a-1 processing by cell extracts, whereas its ectopic expression decreased let-7a production in vivo. Finally, hnRNP A1 binding to let-7a interferes with the binding of KSRP, which is known to promote let-7a biogenesis. We propose that hnRNP A1 and KSRP have antagonistic roles in the post-transcriptional regulation of let-7a expression.

Keywords

Ribonuclease III, Base Sequence, Heterogeneous Nuclear Ribonucleoprotein A1, Recombinant Fusion Proteins, Green Fluorescent Proteins, Molecular Sequence Data, DNA Footprinting, RNA-Binding Proteins, Binding, Competitive, Models, Biological, Article, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Line, Tumor, Heterogeneous-Nuclear Ribonucleoprotein Group A-B, Trans-Activators, Humans, Nucleic Acid Conformation, RNA Processing, Post-Transcriptional, Protein Binding

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    popularity
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    Top 1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
249
Top 1%
Top 10%
Top 1%
Green
hybrid