Evidence map›Paper›PMID 38368736›Full record

ArticleEuropean journal of protistology2024

Single-cell transcriptomic analysis reveals genome evolution in predatory litostomatean ciliates.

Zhaorui Zhou, Chao Li, Qingxiang Yuan, Yong Chi, Yuqing Li, Ying Yan, Saleh A Al-Farraj, Naomi A Stover, Zigui Chen, Xiao Chen

Open access · greenAbstract read
In one paragraph

Article in European journal of protistology, 2024. 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
2.3field-weighted citation impact, top 12% 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. Magnetotaxis in an anaerobic ciliate via tripartite syntrophy.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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 at 5 institutions in 3 countries.

Zhaorui ZhouInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China.
Chao LiInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China.
Qingxiang YuanInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China.
Yong ChiInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China.
Yuqing LiInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China.
Ying YanInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China.
Saleh A Al-FarrajZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Naomi A StoverDepartment of Biology, Bradley University, Peoria 61625, USA. Electronic address: nstover@bradley.edu.
Zigui ChenDepartment of Microbiology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China. Electronic address: zigui.chen@cuhk.edu.hk.
Xiao ChenLaboratory of Marine Protozoan Biodiversity and Evolution, Marine College, Shandong University, Weihai 264209, China; Suzhou Research Institute, Shandong University, Suzhou 215123, China. Electronic address: xc@sdu.edu.cn.
Ocean University of China · CNBradley University · USChinese University of Hong Kong · CNKing Saud University · SAShandong University · CN

Funding

A Resource Center for Tetrahymena ThermophilaP40OD010964 · OD · WASHINGTON UNIVERSITY · PI DOUGLAS LEE CHALKER · 2012 to 2026
$6.5M
NIH HHS P40 OD010964
6 · The paper itself

Abstract

Many ciliated protists prey on other large microbial organisms, including other protists and microscopic metazoans. The ciliate class Litostomatea unites both predatory and endosymbiotic species. The evolution of predation ability in ciliates remains poorly understood, in part, due to a lack of genomic data. To fill this gap, we acquired the transcriptome profiles of six predatory litostomateans using single-cell sequencing technology and investigated their transcriptomic features. Our results show that: (1) in contrast to non-predatory ciliates, the predatory litostomateans have expanded gene families associated with transmembrane activity and reactive oxidative stress response pathways, potentially as a result of cellular behaviors such as fast contraction and extension; (2) the expansion of the calcium-activated BK potassium channel gene family, which hypothetically regulates cell contractility, is an ancient evolutionary event for the class Litostomatea, suggesting a rewired metabolism associated with the hunting behavior of predatory ciliates; and (3) three whole genome duplication (WGD) events have been detected in litostomateans, with genes associated with biosynthetic processes, transmembrane activity, and calcium-activated potassium channel activity being retained during the WGD events. In addition, we explored the evolutionary relationships among 17 ciliate species, including eight litostomateans, and provided a rich foundational dataset for future in-depth phylogenomic studies of Litostomatea. Our comprehensive analyses suggest that the rewired cellular metabolism via expanded gene families and WGD events might be the potential genetic basis for the predation ability of raptorial ciliates.

Indexed as

CiliophoraPredatory BehaviorAnimalsEvolution, MolecularGene Expression ProfilingPhylogenyTranscriptomeGene family expansionLitostomateaPredatory ciliatesSingle-cell transcriptome sequencingWhole genome duplication

Identifiers

PMID38368736
PMCPMC12036533
OpenAlexW4391543328

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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.