Evidence map›Paper›PMID 28655887›Full record

ArticleScientific reports2017

Comparative proteome analysis between C . briggsae embryos and larvae reveals a role of chromatin modification proteins in embryonic cell division.

Xiaomeng An, Jiaofang Shao, Huoming Zhang, Xiaoliang Ren, Vincy Wing Sze Ho, Runsheng Li, Ming-Kin Wong, Zhongying Zhao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 94% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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    Article
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  5. Delineating the mechanisms and design principles ofComputational and structural biotechnology journal · 2022
    Review
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 2 institutions in 3 countries.

Xiaomeng AnDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Jiaofang ShaoDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Huoming ZhangBiosciences Core Laboratory, King Abdullah University of Science and Technology, 23955-6900, Thuwal, Saudi Arabia.ORCID 0000-0001-5416-0358
Xiaoliang RenDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Vincy Wing Sze HoDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Runsheng LiDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Ming-Kin WongDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Zhongying ZhaoDepartment of Biology, Hong Kong Baptist University, Hong Kong, China. zyzhao@hkbu.edu.hk.ORCID 0000-0003-2743-9008
Hong Kong Baptist University · HKKing Abdullah University of Science and Technology · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Caenorhabditis briggsae has emerged as a model for comparative biology against model organism C. elegans. Most of its cell fate specifications are completed during embryogenesis whereas its cell growth is achieved mainly in larval stages. The molecular mechanism underlying the drastic developmental changes is poorly understood. To gain insights into the molecular changes between the two stages, we compared the proteomes between the two stages using iTRAQ. We identified a total of 2,791 proteins in the C. briggsae embryos and larvae, 247 of which undergo up- or down-regulation between the two stages. The proteins that are upregulated in the larval stages are enriched in the Gene Ontology categories of energy production, protein translation, and cytoskeleton; whereas those upregulated in the embryonic stage are enriched in the categories of chromatin dynamics and posttranslational modification, suggesting a more active chromatin modification in the embryos than in the larva. Perturbation of a subset of chromatin modifiers followed by cell lineage analysis suggests their roles in controlling cell division pace. Taken together, we demonstrate a general molecular switch from chromatin modification to metabolism during the transition from C. briggsae embryonic to its larval stages using iTRAQ approach. The switch might be conserved across metazoans.

Indexed as

Cell DivisionProteomeProteomicsAnimalsCaenorhabditisChromatinComputational BiologyData CurationEmbryonic DevelopmentGene OntologyLarvaMass SpectrometryPeptidesPhenotypeRNA InterferenceChromatinPeptidesProteome

Identifiers

PMID28655887
PMCPMC5487359
OpenAlexW2669965642

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.