Evidence map›Paper›PMID 34009621›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2021

Generation and Molecular Characterization of Transient tet1/2/3 Zebrafish Knockouts.

Samuel E Ross, Ozren Bogdanovic

Erratum issuedOpen access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Samuel E RossGenomics and Epigenetics Division, Garvan Institute of Medical Research, Sydney, NSW, Australia.
Ozren BogdanovicGenomics and Epigenetics Division, Garvan Institute of Medical Research, Sydney, NSW, Australia. o.bogdanovic@garvan.org.au.
Garvan Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

5-methylcytosine (5mC) is a gene-regulatory mark associated with transcriptional repression. 5mC can be erased through the catalytic action of Ten-eleven translocation (TET) methylcytosine dioxygenases (TET1, TET2, TET3), which oxidize 5mC resulting in its removal from the genome. In vertebrates, TET enzymes facilitate DNA demethylation of regulatory regions linked to genes involved in developmental processes. Consequently, TET ablation leads to severe morphological defects and developmental arrest. Here we describe a system that can facilitate the study of relationships between TET enzymes, 5mC, and embryo development. We provide detailed descriptions for the generation of F0 zebrafish tet1/2/3 knockouts using CRISPR/Cas9 technology and elaborate on the strategies to assess the impact of TET loss by reduced representation bisulfite sequencing (RRBS).

Indexed as

DNA MethylationGene Expression Regulation, DevelopmentalAnimalsAnimals, Genetically ModifiedDioxygenasesZebrafishZebrafish ProteinsDioxygenasesTet1 protein, zebrafishTET2 protein, zebrafishTET3 protein, zebrafishZebrafish ProteinsCRISPR/Cas9DNA demethylationDNA methylationEmbryogenesisReduced representation bisulfite sequencing (RRBS)TET proteinsZebrafish

Identifiers

PMID34009621
OpenAlexW3163537981

What OpenQuestion holds

Textmetadata
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.