Evidence map›Paper›PMID 41543903›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Towards CRISPR-based editing of the mitochondrial genome in yeast.

Sifei Yin, Daniel F Jarosz, Alice Y Ting

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

3 authors.

Sifei YinDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305.
Daniel F JaroszDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305.ORCID 0000-0003-3497-5888
Alice Y TingDepartment of Genetics, Stanford University, Stanford, CA 94305.ORCID 0000-0002-8277-5226

Funding

Mechanisms of Action of Natural Genetic VariationR01HG012366 · NHGRI · STANFORD UNIVERSITY · PI Daniel Jarosz · 2023 to 2026
$1.5M
Chan Zuckerberg Initiative (CZI) NANHGRI NIH HHS R01 HG012366Stanford University (SU) NA
6 · The paper itself

Abstract

Mitochondria, which evolved from symbiotic bacteria, possess their own genomes (mtDNA) and support independent transcription and translation within the organelle. Given the essential role of mtDNA in energy production, metabolism, as well as cellular homeostasis, and the high density of confirmed pathogenic mutations that map to mtDNA, there is a pressing need for versatile methods to study and manipulate this genome. Although CRISPR technology has revolutionized the editing of nuclear genomes, it has not been successfully extended to mtDNA, primarily due to the challenge of delivering single guide RNAs (sgRNAs) across both outer and inner mitochondrial membranes. Here we develop a survival-based reporter in

Indexed as

CRISPR-Cas SystemsGene EditingGenome, MitochondrialSaccharomyces cerevisiaeAptamers, NucleotideDNA, MitochondrialMitochondriaRNA, Guide, CRISPR-Cas SystemsSaccharomyces cerevisiae ProteinsAptamers, NucleotideDNA, MitochondrialRNA, Guide, CRISPR-Cas SystemsSaccharomyces cerevisiae Proteinsbase editingCRISPR editingmitochondrial gene editingmitochondrial RNA importRNA technology

Identifiers

PMID41543903
PMCPMC12818399

What OpenQuestion holds

Textmetadata
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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.