Evidence map›Paper›PMID 36388977›Full record

ArticleiScience2022

The RNA repair proteins RtcAB regulate transcription activator RtcR via its CRISPR-associated Rossmann fold domain.

Ioly Kotta-Loizou, Maria Grazia Giuliano, Milija Jovanovic, Jorrit Schaefer, Fuzhou Ye, Nan Zhang, Danai Athina Irakleidi, Xiaojiao Liu, Xiaodong Zhang, Martin Buck and 1 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Insights into the structure and function of the RNA ligase RtcB.Cellular and molecular life sciences : CMLS · 2023
    Review
  6. 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

11 authors at 3 institutions in 3 countries.

Ioly Kotta-LoizouDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Maria Grazia GiulianoSchool of Biological and Behavioural Sciences, Queen Mary University of London, London E1 4NS, UK.
Milija JovanovicDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Jorrit SchaeferDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Fuzhou YeSection of Structural Biology, Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
Nan ZhangDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Danai Athina IrakleidiDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Xiaojiao LiuSection of Structural Biology, Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
Xiaodong ZhangSection of Structural Biology, Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
Martin BuckDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Christoph EnglDepartment of Life Sciences, Faculty of Natural Sciences, Imperial College London, London SW7 2AZ, UK.
Imperial College London · GBQueen Mary University of London · GBHouston Methodist · US

Funding

Medical Research Council MR/M017672/1Wellcome Trust
6 · The paper itself

Abstract

CRISPR-associated Rossmann fold (CARF) domain signaling underpins modulation of CRISPR-Cas nucleases; however, the RtcR CARF domain controls expression of two conserved RNA repair enzymes, cyclase RtcA and ligase RtcB. Here, we demonstrate that RtcAB are required for RtcR-dependent transcription activation and directly bind to RtcR CARF. RtcAB catalytic activity is not required for complex formation with CARF, but is essential yet not sufficient for RtcRAB-dependent transcription activation, implying the need for an additional RNA repair-dependent activating signal. This signal differs from oligoadenylates, a known ligand of CARF domains, and instead appears to originate from the translation apparatus: RtcB repairs a tmRNA that rescues stalled ribosomes and increases translation elongation speed. Taken together, our data provide evidence for an expanded range for CARF domain signaling, including the first evidence of its control via

Indexed as

Cell biologyMolecular biologyMolecular mechanism of gene regulation

Identifiers

PMID36388977
PMCPMC9650030
OpenAlexW4306862562

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.