Evidence map›Paper›PMID 36191226›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Mesoscale structure-function relationships in mitochondrial transcriptional condensates.

Marina Feric, Azadeh Sarfallah, Furqan Dar, Dmitry Temiakov, Rohit V Pappu, Tom Misteli

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Learning nature's assembly language with polymers.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Phase separation in mitochondrial fate and mitochondrial diseases.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Review
  11. Condenzymes: Biomolecular condensates with inherent catalytic activities.bioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Emergent microenvironments of nucleoli.Nucleus (Austin, Tex.) · 2024
    Review
  17. Article
  18. Article
  19. Review
  20. 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.

Marina FericNational Cancer Institute, NIH, Bethesda, MD 20892.ORCID 0000-0001-7531-9305
Azadeh SarfallahDepartment of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, PA 19107.
Furqan DarDepartment of Physics, Washington University in St. Louis, St. Louis, MO 63130.
Dmitry TemiakovDepartment of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, PA 19107.ORCID 0000-0001-5497-3068
Rohit V PappuDepartment of Biomedical Engineering, Center for Biomolecular Condensates, Washington University in St. Louis, St. Louis, MO 63130.ORCID 0000-0003-2568-1378
Tom MisteliNational Cancer Institute, NIH, Bethesda, MD 20892.
Johns Hopkins University · USThomas Jefferson University · USWashington University in St. Louis · US

Funding

ROLE OF CHAIN LENGTH AND SEQUENCE CONTEXTS ON POLYGLUTAMINE OLIGOMERIZATIONR01NS056114 · NINDS · WASHINGTON UNIVERSITY · PI PAPPU, ROHIT V · 2007 to 2020
$4.4M
Molecular Mechanisms of Mitochondrial Transcription and ReplicationR35GM131832 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI Dmitry Temiakov · 2019 to 2026
$4.3M
Understanding the Sequence and Structural Determinants of Phase Behavior of ALS-Causing ProteinsR01NS121114 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Tanja Mittag, ROHIT V PAPPU · 2021 to 2026
$3.8M
Functional roles of the phase separation of mitochondrial DNA in agingFI2GM128585 · NIGMS · NATIONAL CANCER INSTITUTE · PI FERIC, MARINA · 2018 to 2018
–
NIGMS NIH HHS FI2 GM128585NIGMS NIH HHS R35 GM131832NINDS NIH HHS R01 NS056114NINDS NIH HHS R01 NS121114
6 · The paper itself

Abstract

In live cells, phase separation is thought to organize macromolecules into membraneless structures known as biomolecular condensates. Here, we reconstituted transcription in condensates from purified mitochondrial components using optimized in vitro reaction conditions to probe the structure-function relationships of biomolecular condensates. We find that the core components of the mt-transcription machinery form multiphasic, viscoelastic condensates in vitro. Strikingly, the rates of condensate-mediated transcription are substantially lower than in solution. The condensate-mediated decrease in transcriptional rates is associated with the formation of vesicle-like structures that are driven by the production and accumulation of RNA during transcription. The generation of RNA alters the global phase behavior and organization of transcription components within condensates. Coarse-grained simulations of mesoscale structures at equilibrium show that the components stably assemble into multiphasic condensates and that the vesicles formed in vitro are the result of dynamical arrest. Overall, our findings illustrate the complex phase behavior of transcribing, multicomponent condensates, and they highlight the intimate, bidirectional interplay of structure and function in transcriptional condensates.

Indexed as

Nuclear BodiesOrganellesMitochondriaRNAStructure-Activity RelationshipRNAbiomolecular condensatesmitochondrial genomephase separationtranscriptionvesicles

Identifiers

PMID36191226
PMCPMC9565167
OpenAlexW4300594403

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.