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      The amphipod crustacean Parhyale hawaiensis: An emerging comparative model of arthropod development, evolution, and regeneration

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          Abstract

          Recent advances in genetic manipulation and genome sequencing have paved the way for a new generation of research organisms. The amphipod crustacean Parhyale hawaiensis is one such system. Parhyale are easy to rear and offer large broods of embryos amenable to injection, dissection, and live imaging. Foundational work has described Parhyale embryonic development, while advancements in genetic manipulation using CRISPR‐Cas9 and other techniques, combined with genome and transcriptome sequencing, have enabled its use in studies of arthropod development, evolution, and regeneration. This study introduces Parhyale development and life history, a catalog of techniques and resources for Parhyale research, and two case studies illustrating its power as a comparative research system.

          This article is categorized under:

          • Comparative Development and Evolution > Evolutionary Novelties

          • Adult Stem Cells, Tissue Renewal, and Regeneration > Regeneration

          • Comparative Development and Evolution > Model Systems

          • Comparative Development and Evolution > Body Plan Evolution

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          Most cited references77

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          A gene complex controlling segmentation in Drosophila.

          E B Lewis (1978)
          The bithorax gene complex in Drosophila contains a minimum of eight genes that seem to code for substances controlling levels of thoracic and abdominal development. The state of repression of at least four of these genes is controlled by cis-regulatory elements and a separate locus (Polycomb) seems to code for a repressor of the complex. The wild-type and mutant segmentation patterns are consistent with an antero-posterior gradient in repressor concentration along the embryo and a proximo-distal gradient along the chromosome in the affinities for repressor of each gene's cis-regulatory element.
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            Construction of transgenic Drosophila by using the site-specific integrase from phage phiC31.

            Amy C. Groth, Matthew Fish, Roel Nusse … (2004)
            The phiC31 integrase functions efficiently in vitro and in Escherichia coli, yeast, and mammalian cells, mediating unidirectional site-specific recombination between its attB and attP recognition sites. Here we show that this site-specific integration system also functions efficiently in Drosophila melanogaster in cultured cells and in embryos. Intramolecular recombination in S2 cells on transfected plasmid DNA carrying the attB and attP recognition sites occurred at a frequency of 47%. In addition, several endogenous pseudo attP sites were identified in the fly genome that were recognized by the integrase and used as substrates for integration in S2 cells. Two lines of Drosophila were created by integrating an attP site into the genome with a P element. phiC31 integrase injected into embryos as mRNA functioned to promote integration of an attB-containing plasmid into the attP site, resulting in up to 55% of fertile adults producing transgenic offspring. A total of 100% of these progeny carried a precise integration event at the genomic attP site. These experiments demonstrate the potential for precise genetic engineering of the Drosophila genome with the phiC31 integrase system and will likely benefit research in Drosophila and other insects.
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              Homeobox genes and axial patterning.

              William McGinnis, Robb Krumlauf (1992)
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                Author and article information

                Contributors
                Nipam H. Patel: npatel@mbl.edu
                Journal
                Journal ID (nlm-ta): Wiley Interdiscip Rev Dev Biol
                Journal ID (iso-abbrev): Wiley Interdiscip Rev Dev Biol
                Journal ID (doi): 10.1111/(ISSN)1759-7692
                Journal ID (publisher-id): WDEV
                Title: Wiley Interdisciplinary Reviews. Developmental Biology
                Publisher: John Wiley & Sons, Inc. (Hoboken, USA )
                ISSN (Print): 1759-7684
                ISSN (Electronic): 1759-7692
                Publication date (Electronic): 11 June 2019
                Publication date (Print): Sep-Oct 2019
                Volume: 8
                Issue: 5 ( doiID: 10.1002/wdev.v8.5 )
                Electronic Location Identifier: e355
                Affiliations
                [ 1 ] Department of Molecular and Cell Biology University of California Berkeley California
                [ 2 ] Marine Biological Laboratory University of Chicago Chicago Illinois
                Author notes
                [*] [* ] Correspondence

                Nipam H. Patel, Marine Biological Laboratory, Woods Hole, MA.

                Email: npatel@ 123456mbl.edu

                Article
                Publisher ID: WDEV355
                DOI: 10.1002/wdev.355
                PMC ID: 6772994
                PubMed ID: 31183976
                SO-VID: e5094229-267d-4f92-864c-d50b6f083d17
                Copyright © © 2019 The Authors. WIREs Developmental Biology published by Wiley Periodicals, Inc.
                License:

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                Date received : 30 October 2018
                Date accepted : 11 May 2019
                Page count
                Figures: 7, Tables: 0, Pages: 20, Words: 13246
                Funding
                Funded by: Division of Graduate Education
                Award ID: 2016230010
                Funded by: Division of Integrative Organismal Systems
                Award ID: 1257379
                Categories
                Subject: Evolutionary Novelties
                Subject: Regeneration
                Subject: Model Systems
                Subject: Body Plan Evolution
                Subject: Advanced Review
                Subject: Advanced Reviews
                Custom metadata
                source-schema-version-number 2.0
                component-id wdev355
                cover-date September/October 2019
                details-of-publishers-convertor Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.9 mode:remove_FC converted:01.10.2019

                Keywords: arthropod,crustacean,development,evodevo,evolution
                Data availability:
                Keywords: arthropod, crustacean, development, evodevo, evolution

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