Evidence map›Paper›PMID 37283088›Full record

ArticleNucleic acids research2023

Widespread CRISPR-derived RNA regulatory elements in CRISPR-Cas systems.

Sergey A Shmakov, Zachary K Barth, Kira S Makarova, Yuri I Wolf, Vyacheslav Brover, Joseph E Peters, Eugene V Koonin

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

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  9. CRISPR-epigenetic crosstalk: From bidirectional regulation to therapeutic potential.Computational and structural biotechnology journal · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Sergey A ShmakovNational Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.
Zachary K BarthDepartment of Microbiology, Cornell University, Ithaca, NY 14853, USA.
Kira S MakarovaNational Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.ORCID 0000-0002-8174-2844
Yuri I WolfNational Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.ORCID 0000-0002-0247-8708
Vyacheslav BroverNational Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.
Joseph E PetersDepartment of Microbiology, Cornell University, Ithaca, NY 14853, USA.
Eugene V KooninNational Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.ORCID 0000-0003-3943-8299
National Center for Biotechnology Information · USCornell University · US

Funding

National Biomedical Information ServicesZIHLM200888 · NLM · NATIONAL LIBRARY OF MEDICINE · PI PALTOO, DINA · 2009 to 2025
$5200.7M
CRISPR/Cas-directed transposition in Tn7-like elementsR01GM129118 · NIGMS · CORNELL UNIVERSITY · PI PETERS, JOSEPH E · 2019 to 2022
$1.2M
NIGMS NIH HHS R01 GM129118
6 · The paper itself

Abstract

CRISPR-cas loci typically contain CRISPR arrays with unique spacers separating direct repeats. Spacers along with portions of adjacent repeats are transcribed and processed into CRISPR(cr) RNAs that target complementary sequences (protospacers) in mobile genetic elements, resulting in cleavage of the target DNA or RNA. Additional, standalone repeats in some CRISPR-cas loci produce distinct cr-like RNAs implicated in regulatory or other functions. We developed a computational pipeline to systematically predict crRNA-like elements by scanning for standalone repeat sequences that are conserved in closely related CRISPR-cas loci. Numerous crRNA-like elements were detected in diverse CRISPR-Cas systems, mostly, of type I, but also subtype V-A. Standalone repeats often form mini-arrays containing two repeat-like sequence separated by a spacer that is partially complementary to promoter regions of cas genes, in particular cas8, or cargo genes located within CRISPR-Cas loci, such as toxins-antitoxins. We show experimentally that a mini-array from a type I-F1 CRISPR-Cas system functions as a regulatory guide. We also identified mini-arrays in bacteriophages that could abrogate CRISPR immunity by inhibiting effector expression. Thus, recruitment of CRISPR effectors for regulatory functions via spacers with partial complementarity to the target is a common feature of diverse CRISPR-Cas systems.

Indexed as

CRISPR-Cas SystemsRNARepetitive Sequences, Nucleic AcidRNA

Identifiers

PMID37283088
PMCPMC10450183
OpenAlexW4379600106

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.