Evidence map›Paper›PMID 42115746›Full record

ArticleThe EMBO journal2026

Short autoinhibitory sequences control phase separation of an essential bacterial transcription termination factor.

Emilia Krypotou, Kiersten M Ruff, Leah K McKinney, Guy E Townsend, Jue D Wang, Rohit V Pappu, Eduardo A Groisman

Abstract read
In one paragraph

Article in The EMBO journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Emilia KrypotouDepartment of Microbial Pathogenesis, Yale School of Medicine, 295 Congress Avenue, New Haven, CT, 06536, USA.
Kiersten M RuffDepartment of Biomedical Engineering and Center for Biomolecular Condensates, James F. McKelvey School of Engineering, Washington University, St. Louis, MO, 63130, USA.
Leah K McKinneyDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID http://orcid.org/0009-0004-5101-8822
Guy E TownsendDepartment of Microbial Pathogenesis, Yale School of Medicine, 295 Congress Avenue, New Haven, CT, 06536, USA.ORCID http://orcid.org/0000-0002-8231-3769
Jue D WangDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID http://orcid.org/0000-0003-1503-170X
Rohit V PappuDepartment of Biomedical Engineering and Center for Biomolecular Condensates, James F. McKelvey School of Engineering, Washington University, St. Louis, MO, 63130, USA. pappu@wustl.edu.ORCID http://orcid.org/0000-0003-2568-1378
Eduardo A GroismanDepartment of Microbial Pathogenesis, Yale School of Medicine, 295 Congress Avenue, New Haven, CT, 06536, USA. eduardo.groisman@yale.edu.ORCID http://orcid.org/0000-0001-6860-7691

Funding

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
Control of gut colonization by the prominent gut bacterium Bacteroides thetaiotaomicronR01GM123798 · NIGMS · YALE UNIVERSITY · PI GROISMAN, EDUARDO · 2018 to 2025
$2.7M
HHS | National Institutes of Health (NIH) R01NS121114HHS | NIH | National Institute of General Medical Sciences (NIGMS) GM123798HHS | NIH | National Institute of General Medical Sciences (NIGMS) GM127088HHS | NIH | National Institute of General Medical Sciences (NIGMS) GM147178NIGMS NIH HHS R01 GM123798US Air Force Office of Scientific Research FA9550-20-1-0241
6 · The paper itself

Abstract

Within cells, across diverse organisms, macromolecular condensation enables spatial and temporal organization of biochemical reactions by organizing proteins and nucleic acids into compositionally distinct membraneless biomolecular condensates. In the gut bacterium Bacteroides thetaiotaomicron, condensate formation by the transcription termination factor Rho (BtRho) increases its termination activity and promotes B. thetaiotaomicron fitness in the mammalian gut. Here, we elucidate the molecular mechanism governing carbon starvation-induced BtRho phase separation. We establish that short, specific amino acid sequences within BtRho's intrinsically disordered region (IDR) control BtRho condensation via complex coacervation. The identified sequences participate in RNA and intra-IDR regulatory interactions that drive condensate formation in vitro and in vivo. We also report that the signaling molecule ppGpp is essential for BtRho phase separation in vivo, binds to purified BtRho in an IDR-dependent manner, and promotes RNA-dependent BtRho condensation in vitro. Our findings demonstrate how specific short sequences within an IDR dictate phase separation in response to nutritional cues.

Indexed as

Bacterial ProteinsRho FactorAmino Acid SequenceGene Expression Regulation, BacterialGuanosine TetraphosphatePhase SeparationBacterial ProteinsGuanosine TetraphosphateRho Factor

Identifiers

PMID42115746
PMCPMC13269538

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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.