UMMS Affiliation
Department of Biochemistry and Molecular Pharmacology
Publication Date
3-15-2018
Document Type
Article
Disciplines
Biochemical Phenomena, Metabolism, and Nutrition | Biochemistry | Bioinformatics | Cell Biology | Developmental Biology | Enzymes and Coenzymes | Genetic Phenomena | Genetics and Genomics | Molecular Biology
Abstract
BACKGROUND: Signaling cascades, such as the extracellular signal-regulated kinase (ERK) pathway, play vital roles in early vertebrate development. Signals through these pathways are initiated by a growth factor or hormone, are transduced through a kinase cascade, and result in the expression of specific downstream genes that promote cellular proliferation, growth, or differentiation. Tight regulation of these signals is provided by positive or negative modulators at varying levels in the pathway, and is required for proper development and function. Two members of the dual-specificity phosphatase (Dusp) family, dusp6 and dusp2, are believed to be negative regulators of the ERK pathway and are expressed in both embryonic and adult zebrafish, but their specific roles in embryogenesis remain to be fully understood.
RESULTS: Using CRISPR/Cas9 genome editing technology, we generated zebrafish lines harboring germ line deletions in dusp6 and dusp2. We do not detect any overt defects in dusp2 mutants, but we find that approximately 50% of offspring from homozygous dusp6 mutants do not proceed through embryonic development. These embryos are fertilized, but are unable to proceed past the first zygotic mitosis and stall at the 1-cell stage for several hours before dying by 10 h post fertilization. We demonstrate that dusp6 is expressed in gonads of both male and female zebrafish, suggesting that loss of dusp6 causes defects in germ cell production. Notably, the 50% of homozygous dusp6 mutants that complete the first cell division appear to progress through embryogenesis normally and give rise to fertile adults.
CONCLUSIONS: The fact that offspring of homozygous dusp6 mutants stall prior to activation of the zygotic genome, suggests that loss of dusp6 affects gametogenesis and/or parentally-directed early development. Further, since only approximately 50% of homozygous dusp6 mutants are affected, we postulate that ERK signaling is tightly regulated and that dusp6 is required to keep ERK signaling within a range that is permissive for proper embryogenesis. Lastly, since dusp6 is expressed throughout zebrafish embryogenesis, but dusp6 mutants do not exhibit defects after the first cell division, it is possible that other regulators of the ERK pathway compensate for loss of dusp6 at later stages.
Keywords
CRISPR, Dual-specific phosphatase, ERK signaling, Germ cell development, MAP kinase phosphatase, Zebrafish embryonic patterning
Rights and Permissions
© The Author(s). 2018. Open Access: This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
DOI of Published Version
10.1186/s12861-018-0164-6
Source
BMC Dev Biol. 2018 Mar 15;18(1):6. doi: 10.1186/s12861-018-0164-6. Link to article on publisher's site
Journal/Book/Conference Title
BMC developmental biology
Related Resources
PubMed ID
29544468
Repository Citation
Maurer, Jennifer M. and Sagerstrom, Charles G., "A parental requirement for dual-specificity phosphatase 6 in zebrafish" (2018). Open Access Articles. 3406.
https://escholarship.umassmed.edu/oapubs/3406
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
Included in
Biochemical Phenomena, Metabolism, and Nutrition Commons, Biochemistry Commons, Bioinformatics Commons, Cell Biology Commons, Developmental Biology Commons, Enzymes and Coenzymes Commons, Genetic Phenomena Commons, Genetics and Genomics Commons, Molecular Biology Commons