Evidence map›Paper›PMID 28723913›Full record

ArticlePloS one2017

Prebiotic selection for motifs in a model of template-free elongation of polymers within compartments.

Grant Kinsler, Sam Sinai, Nicholas Keone Lee, Martin A Nowak

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Synthetic Mutualism and the Intervention Dilemma.Life (Basel, Switzerland) · 2019
    Review
  3. Systems protobiology: origin of life in lipid catalytic networks.Journal of the Royal Society, Interface · 2018
    Review
  4. Primordial sex facilitates the emergence of evolution.Journal of the Royal Society, Interface · 2018
    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.

Grant KinslerDept. Applied Mathematics, School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, United States of America.ORCID http://orcid.org/0000-0001-8308-4665
Sam SinaiProgram for Evolutionary Dynamics, Harvard University, Cambridge, MA, United States of America.
Nicholas Keone LeeDept. Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, United States of America.ORCID http://orcid.org/0000-0002-2756-1102
Martin A NowakProgram for Evolutionary Dynamics, Harvard University, Cambridge, MA, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transition from prelife where self-replication does not occur, to life which exhibits self-replication and evolution, has been a subject of interest for many decades. Membranes, forming compartments, seem to be a critical component of this transition as they provide several concurrent benefits. They maintain localized interactions, generate electro-chemical gradients, and help in selecting cooperative functions as they arise. These functions pave the way for the emergence and maintenance of simple metabolic cycles and polymers. In the context of origin of life, evolution of information-carrying molecules and RNA based enzymes within compartments has been subject to intensive theoretical and experimental research. Hence, many experimental efforts aim to produce compartments that contain elongating polynucleotides (also referred to as protocells), which store information and perform catalysis. Despite impressive experimental progress, we are still relatively ignorant about the dynamics by which elongating polynucleotides can produce more sophisticated behaviors. Here we perform computer simulations to couple information production through template-free elongation of polymers with dividing compartments. We find that polymers with a simple ability-biasing the concentration of monomers within their own compartment-can acquire a selective advantage in prelife. We further investigate whether such a mechanism allows for cooperative dynamics to dominate over purely competitive ones. We show that under this system of biased monomer addition, even without template-directed self-replication, genetic motifs can emerge, compete, cooperate, and ultimately survive within the population.

Indexed as

Biological EvolutionOrigin of LifePolymersPrebioticsArtificial CellsComputer SimulationPolymersPrebiotics

Identifiers

PMID28723913
PMCPMC5516967

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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.