| Literature DB >> 31451030 |
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