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Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
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Eukaryotic RNA Polymerases00:58

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RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
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As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
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Multiple, non-allelic, intein-coding sequences in eukaryotic RNA polymerase genes.

Timothy J D Goodwin1, Margaret I Butler, Russell T M Poulter

  • 1Department of Biochemistry, University of Otago, Dunedin, New Zealand. timg@sanger.otago.ac.nz

BMC Biology
|October 31, 2006
PubMed
Summary

New intein coding sequences were discovered in diverse eukaryotes, expanding their known host range. These findings suggest inteins are ancient elements that occupied conserved sites in proteins across early eukaryotic evolution.

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Area of Science:

  • Molecular Biology
  • Evolutionary Biology
  • Genomics

Background:

  • Inteins are self-splicing protein segments found across life, encoded within host genes.
  • Their distribution is sporadic, with few identified in eukaryotic nuclear genes, primarily from fungi.
  • Inteins excise themselves and ligate flanking extein sequences via a peptide bond.

Purpose of the Study:

  • To identify novel intein coding sequences in eukaryotic nuclear genes.
  • To investigate the evolutionary origins and distribution of inteins in diverse eukaryotes.
  • To understand the preferred insertion sites of inteins within host proteins.

Main Methods:

  • Bioinformatic analysis of nuclear genes encoding RNA polymerase subunits.
  • Comparative sequence analysis of identified intein coding sequences.
  • Phylogenetic analysis to infer evolutionary relationships.

Main Results:

  • Seven intein coding sequences were identified in RNA polymerase subunits (RPA2, RPC2, RPB2) from diverse eukaryotes, including algae and fungi.
  • The first nuclear-encoded inteins outside of fungi were found in Chlamydomonas reinhardtii and Dictyostelium discoideum.
  • Inteins were located in homologous proteins, inserted at multiple conserved regions of RNA polymerase.

Conclusions:

  • The discovery expands the known eukaryotic host range for inteins.
  • Inteins are suggested to be ancient elements widely distributed in early microbial eukaryotes.
  • Inteins persist sporadically, preferentially occupying highly conserved protein regions.