Evidence map›Paper›PMID 34903227›Full record

ArticleBMC biology2021

The hidden genomic diversity of ciliated protists revealed by single-cell genome sequencing.

Wenbing Chen, Changling Zuo, Chundi Wang, Tengteng Zhang, Liping Lyu, Yu Qiao, Fangqing Zhao, Miao Miao

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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  10. Nontriplet feature of genetic code inProceedings of the National Academy of Sciences of the United States of America · 2023
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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

8 authors at 4 institutions in 1 country.

Wenbing Chen *Savaid Medical School, University of Chinese Academy of Sciences, Beijing, 100049, China.
Changling Zuo *Savaid Medical School, University of Chinese Academy of Sciences, Beijing, 100049, China.
Chundi WangInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, 266003, China.
Tengteng ZhangInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, 266003, China.
Liping LyuInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, 266003, China.
Yu QiaoInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, 266003, China.
Fangqing ZhaoSavaid Medical School, University of Chinese Academy of Sciences, Beijing, 100049, China. zhfq@biols.ac.cn.ORCID 0000-0002-6216-1235
Miao MiaoSavaid Medical School, University of Chinese Academy of Sciences, Beijing, 100049, China. miaomiao@ucas.ac.cn.
Ministry of Education of the People's Republic of China · CNChinese Academy of Sciences · CNChina Academy of Chinese Medical Sciences · CNUniversity of Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCiliated protists are a widely distributed, morphologically diverse, and genetically heterogeneous group of unicellular organisms, usually known for containing two types of nuclei: a transcribed polyploid macronucleus involved in gene expression and a silent diploid micronucleus responsible for transmission of genetic material during sexual reproduction and generation of the macronucleus. Although studies in a few species of culturable ciliated protists have revealed the highly dynamic nature of replicative and recombination events relating the micronucleus to the macronucleus, the broader understanding of the genomic diversity of ciliated protists, as well as their phylogenetic relationships and metabolic potential, has been hampered by the inability to culture numerous other species under laboratory conditions, as well as the presence of symbiotic bacteria and microalgae which provide a challenge for current sequencing technologies. Here, we optimized single-cell sequencing methods and associated data analyses, to effectively remove contamination by commensal bacteria, and generated high-quality genomes for a number of Euplotia species.

resultsWe obtained eight high-quality Euplotia genomes by using single-cell genome sequencing techniques. The genomes have high genomic completeness, with sizes between 68 and 125 M and gene numbers between 14K and 25K. Through comparative genomic analysis, we found that there are a large number of gene expansion events in Euplotia genomes, and these expansions are closely related to the phenotypic evolution and specific environmental adaptations of individual species. We further found four distinct subgroups in the genus Euplotes, which exhibited considerable genetic distance and relative lack of conserved genomic syntenies. Comparative genomic analyses of Uronychia and its relatives revealed significant gene expansion associated with the ciliary movement machinery, which may be related to the unique and strong swimming ability.

conclusionsWe employed single-cell genomics to obtain eight ciliate genomes, characterized the underestimated genomic diversity of Euplotia, and determined the divergence time of representative species in this subclass for the first time. We also further investigated the extensive duplication events associated with speciation and environmental adaptation. This study provides a unique and valuable resource for understanding the evolutionary history and genetic diversity of ciliates.

Indexed as

CiliophoraGenomicsChromosome MappingEvolution, MolecularMacronucleusPhylogenyCiliateEuplotiaGenetic diversitySingle-cell genomics

Identifiers

PMID34903227
PMCPMC8670190
OpenAlexW4200547857

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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.