Evidence map›Paper›PMID 36748990›Full record

ArticleG3 (Bethesda, Md.)2023

A high-quality reference genome for the fission yeast Schizosaccharomyces osmophilus.

Guo-Song Jia, Wen-Cai Zhang, Yue Liang, Xi-Han Liu, Nicholas Rhind, Alison Pidoux, Michael Brysch-Herzberg, Li-Lin Du

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Molecular and cellular biology · 2026
    Article
  3. Evolutionary persistence and divergence of thebioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. The micromammals.G3 (Bethesda, Md.) · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. 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

8 authors.

Guo-Song JiaNational Institute of Biological Sciences, Beijing 102206, China.
Wen-Cai ZhangNational Institute of Biological Sciences, Beijing 102206, China.
Yue LiangNational Institute of Biological Sciences, Beijing 102206, China.
Xi-Han LiuNational Institute of Biological Sciences, Beijing 102206, China.
Nicholas RhindDepartment of Biochemistry and Molecular Biotechnology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Alison PidouxWellcome Centre for Cell Biology, Institute of Cell Biology, School of Biological Sciences, The University of Edinburgh, Edinburgh EH9 3BF, Scotland, UK.
Michael Brysch-HerzbergLaboratory for Wine Microbiology, Department International Business, Heilbronn University, Heilbronn 74081, Germany.
Li-Lin DuNational Institute of Biological Sciences, Beijing 102206, China.ORCID 0000-0002-1028-7397

Funding

The Mechanism of Cell Size Regulation - Administrative SupplementR01GM134300 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RHIND, NICHOLAS R · 2020 to 2023
$1.4M
NIGMS NIH HHS R01 GM134300Wellcome Trust 200885Wellcome Trust 200885/Z/16/ZWellcome Trust 203149Wellcome Trust 224358
6 · The paper itself

Abstract

Fission yeasts are an ancient group of fungal species that diverged from each other from tens to hundreds of million years ago. Among them is the preeminent model organism Schizosaccharomyces pombe, which has significantly contributed to our understandings of molecular mechanisms underlying fundamental cellular processes. The availability of the genomes of S. pombe and 3 other fission yeast species S. japonicus, S. octosporus, and S. cryophilus has enabled cross-species comparisons that provide insights into the evolution of genes, pathways, and genomes. Here, we performed genome sequencing on the type strain of the recently identified fission yeast species S. osmophilus and obtained a complete mitochondrial genome and a nuclear genome assembly with gaps only at rRNA gene arrays. A total of 5,098 protein-coding nuclear genes were annotated and orthologs for more than 95% of them were identified. Genome-based phylogenetic analysis showed that S. osmophilus is most closely related to S. octosporus and these 2 species diverged around 16 million years ago. To demonstrate the utility of this S. osmophilus reference genome, we conducted cross-species comparative analyses of centromeres, telomeres, transposons, the mating-type region, Cbp1 family proteins, and mitochondrial genomes. These analyses revealed conservation of repeat arrangements and sequence motifs in centromere cores, identified telomeric sequences composed of 2 types of repeats, delineated relationships among Tf1/sushi group retrotransposons, characterized the evolutionary origins and trajectories of Cbp1 family domesticated transposases, and discovered signs of interspecific transfer of 2 types of mitochondrial selfish elements.

Indexed as

SchizosaccharomycesSchizosaccharomyces pombe ProteinsCentromerePhylogenySchizosaccharomyces pombe Proteinscentromeredouble-hairpin elementfission yeastretrotransposonSchizosaccharomyces osmophilustelomere

Identifiers

PMID36748990
PMCPMC10085805

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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.