Evidence map›Paper›PMID 41331523›Full record

ArticleEMBO reports2026

Cran1, member of a new class of OLD family ATPases, functions in cell cycle progression in an archaeon.

Yunfeng Yang, Shikuan Liang, Junfeng Liu, Xiaofei Fu, Pengju Wu, Haodun Li, Jinfeng Ni, Qunxin She, Mart Krupovic, Yulong Shen

Abstract read
In one paragraph

Article in EMBO reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. The uncharacterizedmicroPublication biology · 2026
    Article
  3. Regulation of eukaryotic-like cell cycle progression in archaea is coming into focus.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

10 authors.

Yunfeng YangCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.ORCID http://orcid.org/0009-0009-6265-2761
Shikuan LiangCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.
Junfeng LiuCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.
Xiaofei FuCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.
Pengju WuCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.
Haodun LiCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.
Jinfeng NiCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.
Qunxin SheCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China.ORCID http://orcid.org/0000-0002-4448-6669
Mart KrupovicInstitut Pasteur, Université Paris Cité, CNRS UMR6047, Cell Biology and Virology of Archaea Unit, Paris, France.ORCID http://orcid.org/0000-0001-5486-0098
Yulong ShenCRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, 266237, Qingdao, China. yulgshen@sdu.edu.cn.ORCID http://orcid.org/0000-0003-3566-0466

Funding

Agence Nationale de la Recherche (ANR) ANR-23-CE13-022EPA EP-C-13-022MOST | National Natural Science Foundation of China (NSFC) 32393973 and 32370033Postdoc Innovation Project of Shandong Province SDCX-ZG-202400122Postdoctoral fellowship Program of CPSF GZC20231471State Key Laboratory of Microbial Technology Open Projects Fund Project NO. M2023-20
6 · The paper itself

Abstract

Overcoming lysogenization defect (OLD) proteins are diverse ATPase-nucleases functioning in antiphage defense in bacteria. However, the role of these proteins in archaea is currently unknown. We describe a new class of archaeal OLD family ATPases and show that they are apparently not involved in antiviral defense but play an essential role in cell cycle progression. The gene for an OLD family enzyme in Saccharolobus islandicus REY15A, named here Cran1 (Cell cycle-related ATPase and nickase 1), cannot be deleted and exhibits cyclic expression patterns at transcriptional and translational levels, with peak expression during the transition from M-G1 to S phase. Cran1 overexpression causes significant growth retardation, cell size enlargement, and increased cellular DNA content. Cran1 displays potent nickase and ATPase activities in vitro, with the nickase activity dependent on the presence of the ATPase domain. Notably, Cran1 copurifies with chromatin-associated proteins, such as Cren7 and a histone deacetylase homolog, suggesting its involvement in chromatin-related activities. Collectively, our results suggest that Cran1 plays an important role in cell cycle progression, revealing a novel function of OLD family proteins.

Indexed as

Adenosine TriphosphatasesArchaeal ProteinsCell CycleGene Expression Regulation, ArchaealAdenosine TriphosphatasesArchaeal ProteinsArchaeaCell Cycle ProgressionChromatinOLD Family ProteinSulfolobales

Identifiers

PMID41331523
PMCPMC12796447

What OpenQuestion holds

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Registered trials

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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.