Evidence map›Paper›PMID 26292216›Full record

ArticleThe Journal of biological chemistry2015

Functional equivalence of an evolutionarily conserved RNA binding module.

Melissa L Wells, Stephanie N Hicks, Lalith Perera, Perry J Blackshear

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Backbone and sidechainBiomolecular NMR assignments · 2022
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Exaptive origins of regulated mRNA decay in eukaryotes.BioEssays : news and reviews in molecular, cellular and developmental biology · 2016
    Review
  14. Emergence and evolution of Zfp36l3.Molecular phylogenetics and evolution · 2016
    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 2 institutions in 1 country.

Melissa L WellsFrom the Signal Transduction Laboratory and.
Stephanie N HicksFrom the Signal Transduction Laboratory and.
Lalith PereraGenome Integrity and Structural Biology Laboratory, NIEHS/National Institutes of Health, Research Triangle Park, North Carolina 27709 and.
Perry J BlackshearFrom the Signal Transduction Laboratory and Departments of Medicine and Biochemistry, Duke University, Medical Center, Durham, North Carolina 27710 black009@niehs.nih.gov.
National Institute of Environmental Health Sciences · USNational Institutes of Health · US

Funding

TTP and related proteins in the regulation of gene expressionZIAES090080 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI BLACKSHEAR, PERRY J · 2009 to 2025
$52.6M
Macromolecular ModelingZICES043010 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI COPELAND, WILLIAM · 2012 to 2025
$5.7M
Intramural NIH HHS
6 · The paper itself

Abstract

Members of the tristetraprolin (TTP) family of proteins participate in the regulation of mRNA turnover after initially binding to AU-rich elements in target mRNAs. Related proteins from most groups of eukaryotes contain a conserved tandem zinc finger (TZF) domain consisting of two closely spaced, similar CCCH zinc fingers that form the primary RNA binding domain. There is considerable sequence variation within the TZF domains from different family members within a single organism and from different organisms, raising questions about sequence-specific effects on RNA binding and decay promotion. We hypothesized that TZF domains from evolutionarily distant species are functionally interchangeable. The single family member expressed in the fission yeast Schizosaccharomyces pombe, Zfs1, promotes the turnover of several dozen transcripts, some of which are involved in cell-cell interactions. Using knockin techniques, we replaced the TZF domain of S. pombe Zfs1 with the equivalent domains from human TTP and the single family member proteins expressed in the silkworm Bombyx mori, the pathogenic yeast Candida guilliermondii, and the plant Chromolaena odorata. We found that the TZF domains from these widely disparate species could completely substitute for the native S. pombe TZF domain, as determined by measurement of target transcript levels and the flocculation phenotype characteristic of Zfs1 deletion. Recombinant TZF domain peptides from several of these species bound to an AU-rich RNA oligonucleotide with comparably high affinity. We conclude that the TZF domains from TTP family members in these evolutionarily widely divergent species are functionally interchangeable in mRNA binding and decay.

Indexed as

Amino Acid SequenceAnimalsAnisotropyEvolution, MolecularGene DeletionGene Knock-In TechniquesGenetic Complementation TestHumansMicroscopy, FluorescenceMolecular Sequence DataNuclear ProteinsPhenotypeProtein BindingProtein Structure, TertiaryRecombinant ProteinsRNANuclear ProteinsRecombinant ProteinsRNARNA, MessengerSchizosaccharomyces pombe ProteinsTristetraprolinZfs1 protein, S pombemRNA decayRNA binding proteinRNA turnoveryeast geneticszinc finger

Identifiers

PMID26292216
PMCPMC4591824
OpenAlexW2197951855

What OpenQuestion holds

Textmetadata
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.