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Updated: May 29, 2026

Analysis of RNA Processing Reactions Using Cell Free Systems: 3' End Cleavage of Pre-mRNA Substrates in vitro
Published on: May 3, 2014
mRNA 3' end processing and more--multiple functions of mammalian cleavage factor I-68
Marc-David Ruepp1, Daniel Schümperli, Silvia M L Barabino
1Institute of Cell Biology, University of Bern, Bern, Switzerland.
Abstract:
The formation of defined 3(') ends is an important step in the biogenesis of mRNAs. In eukaryotic cells, all mRNA 3(') ends are generated by endonucleolytic cleavage of primary transcripts in reactions that are essentially posttranscriptional. Nevertheless, 3(') end formation is tightly connected to transcription in vivo, and a link with mRNA export to the cytoplasm has been postulated. Here, we briefly review the current knowledge about the two types of mRNA 3(') end processing reactions, cleavage/polyadenylation and histone RNA processing. We then focus on factors shared between these two reactions. In particular, we discuss evidence for new functions of the mammalian cleavage factor I subunit CF I(m) 68 in histone RNA 3(') processing and in the export of mature mRNAs from the nucleus to the cytoplasm.
Insights
mRNA 3' end formation is crucial for gene expression. This study reveals new roles for CF I(m) 68 in processing histone RNA and exporting mature messenger RNAs (mRNAs) from the nucleus.
Area of Science:
- Molecular Biology
- Gene Expression
- RNA Processing
Background:
- mRNA 3' end formation is essential for eukaryotic gene expression, occurring post-transcriptionally via endonucleolytic cleavage.
- While post-transcriptional, 3' end processing is linked to transcription and mRNA export.
- Two main types of mRNA 3' end processing exist: cleavage/polyadenylation and histone RNA processing.
Purpose of the Study:
- To review current knowledge on mRNA 3' end processing mechanisms.
- To identify shared factors between cleavage/polyadenylation and histone RNA processing.
- To investigate novel functions of CF I(m) 68 in histone RNA processing and mRNA export.
Main Methods:
- Literature review of mRNA 3' end biogenesis.
- Focus on shared factors in RNA processing pathways.
- Analysis of the role of mammalian cleavage factor I subunit CF I(m) 68.
Main Results:
- Evidence suggests CF I(m) 68 has new functions in histone RNA 3' processing.
- CF I(m) 68 is implicated in the export of mature mRNAs from the nucleus to the cytoplasm.
- Shared factors contribute to the coordination of transcription, processing, and export.
Conclusions:
- CF I(m) 68 plays a dual role in RNA metabolism, impacting both histone RNA processing and mRNA export.
- Understanding shared factors like CF I(m) 68 provides insights into the intricate regulation of gene expression.
- This research highlights the interconnectedness of mRNA processing and nuclear export pathways.
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