Evidence map›Paper›PMID 34663436›Full record

ArticleGenome biology2021

Effects of sequence motifs in the yeast 3' untranslated region determined from massively parallel assays of random sequences.

Andrew Savinov, Benjamin M Brandsen, Brooke E Angell, Josh T Cuperus, Stanley Fields

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
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  9. Impact on splicing inRNA (New York, N.Y.) · 2023
    Article
  10. Article
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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

5 authors at 3 institutions in 1 country.

Andrew SavinovDepartment of Genome Sciences, University of Washington, Box 355065, Seattle, WA, 98195, USA.
Benjamin M BrandsenDepartment of Genome Sciences, University of Washington, Box 355065, Seattle, WA, 98195, USA.
Brooke E AngellDepartment of Genome Sciences, University of Washington, Box 355065, Seattle, WA, 98195, USA.
Josh T CuperusDepartment of Genome Sciences, University of Washington, Box 355065, Seattle, WA, 98195, USA. cuperusj@uw.edu.
Stanley FieldsDepartment of Genome Sciences, University of Washington, Box 355065, Seattle, WA, 98195, USA. fields@uw.edu.ORCID 0000-0001-5504-5925
University of Washington · USCreighton University · USNorthwestern University · US

Funding

Modeling gene expression in yeast using large degenerate librariesR01GM125809 · NIGMS · UNIVERSITY OF WASHINGTON · PI FIELDS, STANLEY · 2018 to 2021
$1.4M
NIGMS NIH HHS R01 GM125809
6 · The paper itself

Abstract

backgroundThe 3' untranslated region (UTR) plays critical roles in determining the level of gene expression through effects on activities such as mRNA stability and translation. Functional elements within this region have largely been identified through analyses of native genes, which contain multiple co-evolved sequence features.

resultsTo explore the effects of 3' UTR sequence elements outside of native sequence contexts, we analyze hundreds of thousands of random 50-mers inserted into the 3' UTR of a reporter gene in the yeast Saccharomyces cerevisiae. We determine relative protein expression levels from the fitness of transformants in a growth selection. We find that the consensus 3' UTR efficiency element significantly boosts expression, independent of sequence context; on the other hand, the consensus positioning element has only a small effect on expression. Some sequence motifs that are binding sites for Puf proteins substantially increase expression in the library, despite these proteins generally being associated with post-transcriptional downregulation of native mRNAs. Our measurements also allow a systematic examination of the effects of point mutations within efficiency element motifs across diverse sequence backgrounds. These mutational scans reveal the relative in vivo importance of individual bases in the efficiency element, which likely reflects their roles in binding the Hrp1 protein involved in cleavage and polyadenylation.

conclusionsThe regulatory effects of some 3' UTR sequence features, like the efficiency element, are consistent regardless of sequence context. In contrast, the consequences of other 3' UTR features appear to be strongly dependent on their evolved context within native genes.

Indexed as

3' Untranslated RegionsBinding SitesGene LibraryHigh-Throughput Nucleotide SequencingNucleotide MotifsPoly UProtein BiosynthesisRNA-Binding ProteinsRNA, MessengerRNA StabilitySaccharomyces cerevisiaeSaccharomyces cerevisiae Proteins3' Untranslated RegionsPoly URNA-Binding ProteinsRNA, MessengerSaccharomyces cerevisiae Proteins3′ untranslated regionEfficiency elementMassively parallel reporter assaymRNA processingPuf protein

Identifiers

PMID34663436
PMCPMC8522215
OpenAlexW3206911517

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.