Evidence map›Paper›PMID 22562198›Full record

ArticleThe International journal of developmental biology2012

The zebrafish sf3b1b460 mutant reveals differential requirements for the sf3b1 pre-mRNA processing gene during neural crest development.

Min An, Paul D Henion

Open access · bronzeAbstract read
In one paragraph

Article in The International journal of developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  16. Identification of recurrent mutational events in anorectal melanoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2017
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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

2 authors at 1 institution in 1 country.

Min AnDepartment of Neuroscience, Ohio State University, Columbus, OH 43210, USA.
Paul D Henion
The Ohio State University · US

Funding

Development of Distinct Neural Crest and Hematopoietic SubpopulationsR01GM076505 · NIGMS · OHIO STATE UNIVERSITY · PI HENION, PAUL D · 2006 to 2009
$1.1M
Gene Function Profiling of Neural Crest Cell DiversificationR21DE023294 · NIDCR · OHIO STATE UNIVERSITY · PI BEATTIE, CHRISTINE E · 2012 to 2013
$412k
mRNA peptide display as a tool for drug discoveryF32GM074505 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI SEEBECK, FLORIAN · 2005 to 2007
$112k
NIDCR NIH HHS R21 DE023294NIGMS NIH HHS F32 GM074505NIGMS NIH HHS GM074505NIGMS NIH HHS R01 GM076505
6 · The paper itself

Abstract

The functions of gene regulatory networks that control embryonic cell diversification occur on a background of constitutively active molecular machinery necessary for the elaboration of genetic interactions. The essential roles of subsets of such "housekeeping" genes in the regulation of specific aspects of development have become increasingly clear. Pre-mRNA processing is essential for production of functional transcripts by, for example, excision of introns. We have cloned the zebrafish toast(b460) locus and found that it encodes splicing factor 3b, subunit 1 (sf3b1). The sf3b1(b460) mutation causes aberrant splicing of sf3b1 resulting in functional and predicted non-functional transcripts and a 90% reduction in full-length Sf3b1 protein. The sf3b1(b460) mutation was isolated in a mutagenesis screen based on the absence of neural crest-derived melanophores. Further analysis revealed specific earlier defects in neural crest development, whereas the early development of other ectodermal populations appears unaffected. The expression of essential transcriptional regulators of neural crest development are severely disrupted in sf3b1(b460) mutants, due in part to defects in pre-mRNA processing of a subset of these factors, leading to defects in neural crest sublineage specification, survival and migration. Misexpression of a subset of these factors rescues aspects of neural crest development in mutant embryos. Our results indicate that although sf3b1 is a ubiquitously essential gene, the degree to which it is required exhibits tissue-type specificity during early embryogenesis. Further, the developmental defects caused by the sf3b1(b460) mutation provide insights into genetic interactions among members of the gene regulatory network controlling neural crest development.

Indexed as

MutationAmino Acid SequenceAnimalsApoptosisBase SequenceBlotting, WesternEmbryo, NonmammalianGene Expression Regulation, DevelopmentalImmunohistochemistryIn Situ HybridizationMelanophoresMolecular Sequence DataNeural CrestReverse Transcriptase Polymerase Chain ReactionRNA-Binding ProteinsRNA PrecursorsRNA-Binding ProteinsRNA PrecursorsRNA Splice SitesRNA Splicing FactorsSf3b1 protein, zebrafishZebrafish Proteins

Identifiers

PMID22562198
PMCPMC3750977
OpenAlexW2016009114

What OpenQuestion holds

Textmetadata
LicenceTDM
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.