Evidence map›Paper›PMID 31318034›Full record

ArticleIntegrative and comparative biology2019

Complex Transmission Patterns and Age-Related Dynamics of a Selfish mtDNA Deletion.

Jennifer A Sullins, Anna L Coleman-Hulbert, Alexandra Gallegos, Dana K Howe, Dee R Denver, Suzanne Estes

Open access · bronzeAbstract read
In one paragraph

Article in Integrative and comparative biology, 2019. 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 44% 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. Article
  2. Review
  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

6 authors at 3 institutions in 1 country.

Jennifer A SullinsDepartment of Biology, Portland State University, Portland, OR 97201, USA.
Anna L Coleman-HulbertInstitute for Ecology and Evolution, University of Oregon, Eugene, OR 97403, USA.
Alexandra GallegosDepartment of Biology, Portland State University, Portland, OR 97201, USA.
Dana K HoweDepartment of Integrative Biology, Oregon State University, Corvallis, OR 97331, USA.
Dee R DenverDepartment of Integrative Biology, Oregon State University, Corvallis, OR 97331, USA.
Suzanne EstesDepartment of Biology, Portland State University, Portland, OR 97201, USA.
Portland State University · USOregon State University · USUniversity of Oregon · US

Funding

Mutational and evolutionary impact of mitochondrial dysfunctionR01GM087628 · NIGMS · OREGON STATE UNIVERSITY · PI DENVER, DEE, ESTES, SUZANNE R · 2010 to 2014
$1.4M
NIGMS NIH HHS R01 GM087628
6 · The paper itself

Abstract

Despite wide-ranging implications of selfish mitochondrial DNA (mtDNA) elements for human disease and topics in evolutionary biology (e.g., speciation), the forces controlling their formation, age-related accumulation, and offspring transmission remain largely unknown. Selfish mtDNA poses a significant challenge to genome integrity, mitochondrial function, and organismal fitness. For instance, numerous human diseases are associated with mtDNA mutations; however, few genetic systems can simultaneously represent pathogenic mitochondrial genome evolution and inheritance. The nematode Caenorhabditis briggsae is one such system. Natural C. briggsae isolates harbor varying levels of a large-scale deletion affecting the mitochondrial nduo-5 gene, termed nad5Δ. A subset of these isolates contains putative compensatory mutations that may reduce the risk of deletion formation. We studied the dynamics of nad5Δ heteroplasmy levels during animal development and transmission from mothers to offspring in genetically diverse C. briggsae natural isolates. Results support previous work demonstrating that nad5Δ is a selfish element and that heteroplasmy levels of this deletion can be quite plastic, exhibiting high degrees of inter-family variability and divergence between generations. The latter is consistent with a mitochondrial bottleneck effect, and contrasts with previous findings from a laboratory-derived model uaDf5 mtDNA deletion in C. elegans. However, we also found evidence for among-isolate differences in the ability to limit nad5Δ accumulation, the pattern of which suggested that forces other than the compensatory mutations are important in protecting individuals and populations from rampant mtDNA deletion expansion over short time scales.

Indexed as

Gene DeletionAge FactorsAnimalsCaenorhabditisDNA, MitochondrialMaternal InheritanceRepetitive Sequences, Nucleic AcidDNA, Mitochondrial

Identifiers

PMID31318034
PMCPMC6797909
OpenAlexW2963374717

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.