Evidence map›Paper›PMID 28961820›Full record

ArticleMolecular biology and evolution2017

Diminishing Returns on Intragenic Repeat Number Expansion in the Production of Signaling Peptides.

David W Rogers, Ellen McConnell, Eric L Miller, Duncan Greig

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Pheromone Response and Mating Behavior in Fission Yeast.Microbiology and molecular biology reviews : MMBR · 2022
    Review
  2. Article
  3. 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 2 countries.

David W RogersExperimental Evolution Research Group, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Ellen McConnellExperimental Evolution Research Group, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Eric L MillerExperimental Evolution Research Group, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Duncan GreigExperimental Evolution Research Group, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Max Planck Institute for Evolutionary Biology · DEUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signaling peptides enable communication between cells, both within and between individuals, and are therefore key to the control of complex physiological and behavioral responses. Since their small sizes prevent direct transmission to secretory pathways, these peptides are often produced as part of a larger polyprotein comprising precursors for multiple related or identical peptides; the physiological and behavioral consequences of this unusual gene structure are not understood. Here, we show that the number of mature-pheromone-encoding repeats in the yeast α-mating-factor gene MFα1 varies considerably between closely related isolates of both Saccharomyces cerevisiae and its sister species Saccharomyces paradoxus. Variation in repeat number has important phenotypic consequences: Increasing repeat number caused higher pheromone production and greater competitive mating success. However, the magnitude of the improvement decreased with increasing repeat number such that repeat amplification beyond that observed in natural isolates failed to generate more pheromone, and could actually reduce sexual fitness. We investigate multiple explanations for this pattern of diminishing returns and find that our results are most consistent with a translational trade-off: Increasing the number of encoded repeats results in more mature pheromone per translation event, but also generates longer transcripts thereby reducing the rate of translation-a phenomenon known as length-dependent translation. Length-dependent translation may be a powerful constraint on the evolution of genes encoding repetitive or modular proteins, with important physiological and behavioral consequences across eukaryotes.

Indexed as

Amino Acid SequenceCodonDNA Copy Number VariationsEvolution, MolecularGenetic Association StudiesPeptidesPheromonesProtein PrecursorsProtein Sorting SignalsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionTandem Repeat SequencesCodonMF(ALPHA)1 protein, S cerevisiaePeptidesPheromonesProtein PrecursorsProtein Sorting SignalsSaccharomyces cerevisiae Proteinscodon usageconcerted evolutioncopy number variationgenotype-to-phenotypelength-dependent translationprotein tandem repeats

Identifiers

PMID28961820
PMCPMC5850478
OpenAlexW2754582945

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.