Evidence map›Paper›PMID 26735411›Full record

ArticleTranscription2016

A model for genesis of transcription systems.

Zachary F Burton, Kristopher Opron, Guowei Wei, James H Geiger

Open access · hybridAbstract read
In one paragraph

Article in Transcription, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Non-continuum Nature of Eukaryotic Transcriptional Regulation.Advances in experimental medicine and biology · 2022
    Article
  5. Evolution of the genetic code.Transcription · 2021
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Recruitment of CRISPR-Cas systems by Tn7-like transposons.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Zachary F Burtona Department of Biochemistry and Molecular Biology , Michigan State University , E. Lansing , MI , USA.
Kristopher Opronb Department of Mathematics , Michigan State University , E. Lansing , MI , USA.
Guowei Weib Department of Mathematics , Michigan State University , E. Lansing , MI , USA.
James H Geigerc Department of Chemistry , Michigan State University , E. Lansing , MI , USA.
Michigan State University · US

Funding

Multiscale modeling of supramolecular protein-DNA assembliesR01GM092949 · NIGMS · MICHIGAN STATE UNIVERSITY · PI FEIG, MICHAEL · 2010 to 2013
$1.1M
NIGMS NIH HHS R01 GM092949
6 · The paper itself

Abstract

Repeating sequences generated from RNA gene fusions/ligations dominate ancient life, indicating central importance of building structural complexity in evolving biological systems. A simple and coherent story of life on earth is told from tracking repeating motifs that generate α/β proteins, 2-double-Ψ-β-barrel (DPBB) type RNA polymerases (RNAPs), general transcription factors (GTFs), and promoters. A general rule that emerges is that biological complexity that arises through generation of repeats is often bounded by solubility and closure (i.e., to form a pseudo-dimer or a barrel). Because the first DNA genomes were replicated by DNA template-dependent RNA synthesis followed by RNA template-dependent DNA synthesis via reverse transcriptase, the first DNA replication origins were initially 2-DPBB type RNAP promoters. A simplifying model for evolution of promoters/replication origins via repetition of core promoter elements is proposed. The model can explain why Pribnow boxes in bacterial transcription (i.e., (-12)TATAATG(-6)) so closely resemble TATA boxes (i.e., (-31)TATAAAAG(-24)) in archaeal/eukaryotic transcription. The evolution of anchor DNA sequences in bacterial (i.e., (-35)TTGACA(-30)) and archaeal (BRE(up); BRE for TFB recognition element) promoters is potentially explained. The evolution of BRE(down) elements of archaeal promoters is potentially explained.

Indexed as

Promoter Regions, GeneticTranscription, GeneticArchaeal ProteinsBacterial ProteinsBinding SitesDNA-Directed RNA PolymerasesEvolution, MolecularModels, MolecularProtein ConformationProtein Structure, TertiaryReplication OriginTranscription FactorsArchaeal ProteinsBacterial ProteinsDNA-Directed RNA PolymerasesTranscription Factorscradle-loop barrel metafolddouble-Ψ−β-barrelsgeneral transcription factorsLECA (the last eukaryotic common ancestor)LUCA (the last universal common cellular ancestor)replicationRIFT barrelsRNA polymeraseRossmann foldsTATA-binding protein (TBP)the carboxy terminal domain (CTD) of RNA polymerase IITIM barrelstranscriptiontranscription factor B (TFB)α/β protein foldsσ factors

Identifiers

PMID26735411
PMCPMC4802759
OpenAlexW2231501376

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.