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Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
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Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
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A Reporter Based Cellular Assay for Monitoring Splicing Efficiency
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RNA structure in splicing: An evolutionary perspective.

Chien-Ling Lin1, Allison J Taggart1, William G Fairbrother1,2,3

  • 1a Molecular Biology, Cell Biology and Biochemistry, Brown University , Providence , RI , USA.

RNA Biology
|July 26, 2016
PubMed
Summary
This summary is machine-generated.

Highly structured introns, found in fish and humans, can self-regulate pre-mRNA splicing. These RNA structures, formed by complementary repeats, may enhance gene expression robustness and evolve rapidly.

Keywords:
Dinucleotide repeatsU2AF2intron secondary structurepre-mRNA splicingsingle nucleotide polymorphism

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Area of Science:

  • Molecular Biology
  • Genetics
  • RNA Biology

Background:

  • Pre-messenger RNA (pre-mRNA) splicing is a critical post-transcriptional regulatory process.
  • Introns are removed, and exons are joined during splicing.
  • A novel class of structured introns has been identified in fish.

Purpose of the Study:

  • To discuss the prevalence and potential functions of highly structured introns.
  • To explore the role of structured introns in gene regulation.
  • To investigate the evolutionary dynamics of structured introns.

Main Methods:

  • Analysis of intron structures formed by complementary dimer repeats (AC and GT).
  • Examination of structured introns in fish and human genomes, including HLA receptor genes.
  • Investigation of the relationship between intron structure, splicing factor binding, and gene polymorphism.

Main Results:

  • Structured introns can form bridging structures that ensure correct splice site pairing.
  • Some fish introns exhibit structures strong enough to splice without regulatory proteins.
  • In humans, structured introns often result from C and G-rich repeats at intron boundaries.
  • Structured introns in HLA receptor genes enhance transcript processing robustness.
  • Highly polymorphic receptor genes frequently contain structured introns.

Conclusions:

  • Structured introns represent a significant mechanism for regulating pre-mRNA splicing.
  • These RNA structures contribute to gene expression robustness, particularly in highly polymorphic genes.
  • The composition of structured introns from simple repeats suggests they are rapidly evolving genetic elements.