Evidence map›Paper›PMID 34599243›Full record

ArticleScientific reports2021

Crossing design shapes patterns of genetic variation in synthetic recombinant populations of Saccharomyces cerevisiae.

Mark A Phillips, Ian C Kutch, Kaitlin M McHugh, Savannah K Taggard, Molly K Burke

Abstract read
In one paragraph

Article in Scientific reports, 2021. 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
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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.

Mark A PhillipsDepartment of Integrative Biology, Oregon State University, Corvallis, OR, 97331, USA. philmark@oregonstate.edu.
Ian C KutchDepartment of Integrative Biology, Oregon State University, Corvallis, OR, 97331, USA.
Kaitlin M McHughDepartment of Integrative Biology, Oregon State University, Corvallis, OR, 97331, USA.
Savannah K TaggardDepartment of Integrative Biology, Oregon State University, Corvallis, OR, 97331, USA.
Molly K BurkeDepartment of Integrative Biology, Oregon State University, Corvallis, OR, 97331, USA. molly.burke@oregonstate.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

"Synthetic recombinant" populations have emerged as a useful tool for dissecting the genetics of complex traits. They can be used to derive inbred lines for fine QTL mapping, or the populations themselves can be sampled for experimental evolution. In the latter application, investigators generally value maximizing genetic variation in constructed populations. This is because in evolution experiments initiated from such populations, adaptation is primarily fueled by standing genetic variation. Despite this reality, little has been done to systematically evaluate how different methods of constructing synthetic populations shape initial patterns of variation. Here we seek to address this issue by comparing outcomes in synthetic recombinant Saccharomyces cerevisiae populations created using one of two strategies: pairwise crossing of isogenic strains or simple mixing of strains in equal proportion. We also explore the impact of the varying the number of parental strains. We find that more genetic variation is initially present and maintained when population construction includes a round of pairwise crossing. As perhaps expected, we also observe that increasing the number of parental strains typically increases genetic diversity. In summary, we suggest that when constructing populations for use in evolution experiments, simply mixing founder strains in equal proportion may limit the adaptive potential.

Indexed as

Crosses, GeneticGenetic EngineeringGenetic VariationAllelesGene FrequencyGenome, FungalGenomicsGenotypePolymorphism, Single NucleotideRecombinant ProteinsSaccharomyces cerevisiaeWhole Genome SequencingRecombinant Proteins

Identifiers

PMID34599243
PMCPMC8486856

What Socratic holds

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Registered trials

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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 Socratic graph.