Evidence map›Paper›PMID 32548116›Full record

ArticleFrontiers in cell and developmental biology2020

Tissue-Specific Requirement for the GINS Complex During Zebrafish Development.

Máté Varga, Kitti Csályi, István Bertyák, Dóra K Menyhárd, Richard J Poole, Kara L Cerveny, Dorottya Kövesdi, Balázs Barátki, Hannah Rouse, Zsuzsa Vad and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. 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
0.3field-weighted citation impact, top 47% 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, 8 citations in OpenAlex.

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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

16 authors at 5 institutions in 4 countries.

Máté VargaDepartment of Genetics, ELTE Eötvös Loránd University, Budapest, Hungary.
Kitti CsályiDepartment of Genetics, ELTE Eötvös Loránd University, Budapest, Hungary.
István BertyákDepartment of Genetics, ELTE Eötvös Loránd University, Budapest, Hungary.
Dóra K MenyhárdHAS-ELTE Protein Modeling Research Group and Laboratory of Structural Chemistry and Biology, ELTE Eötvös Loránd University, Budapest, Hungary.
Richard J PooleDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
Kara L CervenyBiology Department, Reed College, Portland, OR, United States.
Dorottya KövesdiOffice of Supported Research Groups of the Hungarian Academy of Sciences, Budapest, Hungary.
Balázs BarátkiDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Hannah RouseDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
Zsuzsa VadDepartment of Genetics, ELTE Eötvös Loránd University, Budapest, Hungary.
Thomas A HawkinsDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
Heather L StickneyDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
Florencia CavodeassiDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
Quenten SchwarzCentre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, Australia.
Rodrigo M YoungDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
Stephen W WilsonDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, United Kingdom.
University College London · GBEötvös Loránd University · HUHungarian Academy of Sciences · HUReed College · USSouth Australia Pathology · AU

Funding

Medical Research Council G0900994Medical Research Council MR/L003775/1Medical Research Council MR/T020164/1Wellcome Trust 207483/Z/17/Z
6 · The paper itself

Abstract

Efficient and accurate DNA replication is particularly critical in stem and progenitor cells for successful proliferation and survival. The replisome, an amalgam of protein complexes, is responsible for binding potential origins of replication, unwinding the double helix, and then synthesizing complimentary strands of DNA. According to current models, the initial steps of DNA unwinding and opening are facilitated by the CMG complex, which is composed of a GINS heterotetramer that connects Cdc45 with the mini-chromosome maintenance (Mcm) helicase. In this work, we provide evidence that in the absence of GINS function DNA replication is cell autonomously impaired, and we also show that

Indexed as

CMG complexGINS2GINS complexproliferationreplicationzebrafish

Identifiers

PMID32548116
PMCPMC7270345
OpenAlexW3032213934

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.