Literature DB >> 31451030

Genetic compensation by epob in pronephros development in epoa mutant zebrafish.

Jianqing She1,2, Yue Wu1, Bowen Lou1,2, Elisabeth Lodd2, Alina Klems3, Felix Schmoehl2, Zuyi Yuan1, Ferdinand Le Noble3, Jens Kroll2.   

Abstract

Zebrafish erythropoietin a (epoa) is a well characterized regulator of red blood cell formation. Recent morpholino mediated knockdown data have also identified epoa being essential for physiological pronephros development in zebrafish, which is driven by blocking apoptosis in developing kidneys. Yet, zebrafish mutants for epoa have not been described so far. In order to compare a transient knockdown vs. permanent knockout for epoa in zebrafish on pronephros development, we used CRISPR/Cas9 technology to generate epoa knockout zebrafish mutants and we performed structural and functional studies on pronephros development. In contrast to epoa morphants, epoa-/- zebrafish mutants showed normal pronephros structure; however, a previously uncharacterized gene in zebrafish, named epob, was identified and upregulated in epoa-/- mutants. epob knockdown altered pronephros development, which was further aggravated in epoa-/- mutants. Likewise, epoa and epob morphants regulated similar and differential gene signatures related to kidney development in zebrafish. In conclusion, stable loss of epoa during embryonic development can be compensated by epob leading to phenotypical discrepancies in epoa knockdown and knockout zebrafish embryos.

Entities:  

Keywords:  Erythropoietin; compensation; gene knockout; kidney development; zebrafish

Year:  2019        PMID: 31451030      PMCID: PMC6773226          DOI: 10.1080/15384101.2019.1656019

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  33 in total

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Journal:  Development       Date:  2014-08       Impact factor: 6.868

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Journal:  Nature       Date:  2014-12-10       Impact factor: 49.962

5.  Structural characterization of human erythropoietin.

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Journal:  Development       Date:  1999-08       Impact factor: 6.868

Review 7.  Zebrafish as a Model for the Study of Microvascular Complications of Diabetes and Their Mechanisms.

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8.  A systematic genome-wide analysis of zebrafish protein-coding gene function.

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Journal:  Nature       Date:  2013-04-17       Impact factor: 49.962

9.  Structural mechanism of transcription regulation of the Staphylococcus aureus multidrug efflux operon mepRA by the MarR family repressor MepR.

Authors:  Ivan Birukou; Susan M Seo; Bryan D Schindler; Glenn W Kaatz; Richard G Brennan
Journal:  Nucleic Acids Res       Date:  2013-11-28       Impact factor: 16.971

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  1 in total

Review 1.  Genotype to Phenotype: CRISPR Gene Editing Reveals Genetic Compensation as a Mechanism for Phenotypic Disjunction of Morphants and Mutants.

Authors:  Cristy M Salanga; Matthew C Salanga
Journal:  Int J Mol Sci       Date:  2021-03-27       Impact factor: 5.923

  1 in total

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