Literature DB >> 33482173

CRISPR-Cas9 editing of non-coding genomic loci as a means of controlling gene expression in the sea urchin.

Alice Pieplow1, Meseret Dastaw2, Tetsushi Sakuma3, Naoaki Sakamoto3, Takashi Yamamoto3, Mamiko Yajima1, Nathalie Oulhen1, Gary M Wessel4.   

Abstract

We seek to manipulate gene function here through CRISPR-Cas9 editing of cis-regulatory sequences, rather than the more typical mutation of coding regions. This approach would minimize secondary effects of cellular responses to nonsense mediated decay pathways or to mutant protein products by premature stops. This strategy also allows for reducing gene activity in cases where a complete gene knockout would result in lethality, and it can be applied to the rapid identification of key regulatory sites essential for gene expression. We tested this strategy here with genes of known function as a proof of concept, and then applied it to examine the upstream genomic region of the germline gene Nanos2 in the sea urchin, Strongylocentrotus purpuratus. We first used CRISPR-Cas9 to target established genomic cis-regulatory regions of the skeletogenic cell transcription factor, Alx1, and the TGF-β signaling ligand, Nodal, which produce obvious developmental defects when altered in sea urchin embryos. Importantly, mutation of cis-activator sites (Alx1) and cis-repressor sites (Nodal) result in the predicted decreased and increased transcriptional output, respectively. Upon identification of efficient gRNAs by genomic mutations, we then used the same validated gRNAs to target a deadCas9-VP64 transcriptional activator to increase Nodal transcription directly. Finally, we paired these new methodologies with a more traditional, GFP reporter construct approach to further our understanding of the transcriptional regulation of Nanos2, a key gene required for germ cell identity in S. purpuratus. With a series of reporter assays, upstream Cas9-promoter targeted mutagenesis, coupled with qPCR and in situ RNA hybridization, we concluded that the promoter of Nanos2 drives strong mRNA expression in the sea urchin embryo, indicating that its primordial germ cell (PGC)-specific restriction may rely instead on post-transcriptional regulation. Overall, we present a proof-of-principle tool-kit of Cas9-mediated manipulations of promoter regions that should be applicable in most cells and embryos for which CRISPR-Cas9 is employed.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alx1; CRISPR/Cas9; Cis-regulatory elements; Germ line; Nanos; Nodal; Primordial germ cells; Sea urchin; Transcriptional regulation

Mesh:

Substances:

Year:  2021        PMID: 33482173      PMCID: PMC7956150          DOI: 10.1016/j.ydbio.2021.01.003

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  72 in total

1.  R11: a cis-regulatory node of the sea urchin embryo gene network that controls early expression of SpDelta in micromeres.

Authors:  Roger Revilla-i-Domingo; Takuya Minokawa; Eric H Davidson
Journal:  Dev Biol       Date:  2004-10-15       Impact factor: 3.582

2.  Drosophila Pumilio protein contains multiple autonomous repression domains that regulate mRNAs independently of Nanos and brain tumor.

Authors:  Chase A Weidmann; Aaron C Goldstrohm
Journal:  Mol Cell Biol       Date:  2011-11-07       Impact factor: 4.272

3.  A hyaline layer protein that becomes localized to the oral ectoderm and foregut of sea urchin embryos.

Authors:  J A Coffman; D R McClay
Journal:  Dev Biol       Date:  1990-07       Impact factor: 3.582

Review 4.  Microinjection methods for sea urchin eggs and blastomeres.

Authors:  Junko Yaguchi
Journal:  Methods Cell Biol       Date:  2019-01-28       Impact factor: 1.441

5.  Albinism as a visual, in vivo guide for CRISPR/Cas9 functionality in the sea urchin embryo.

Authors:  Nathalie Oulhen; Gary M Wessel
Journal:  Mol Reprod Dev       Date:  2016-11-30       Impact factor: 2.609

6.  Distinct transcriptional regulation of Nanos2 in the germ line and soma by the Wnt and delta/notch pathways.

Authors:  Nathalie Oulhen; S Zachary Swartz; Lingyu Wang; Athula Wikramanayake; Gary M Wessel
Journal:  Dev Biol       Date:  2019-05-07       Impact factor: 3.582

7.  The 3'UTR of nanos2 directs enrichment in the germ cell lineage of the sea urchin.

Authors:  Nathalie Oulhen; Takaya Yoshida; Mamiko Yajima; Jia L Song; Tetsushi Sakuma; Naoaki Sakamoto; Takashi Yamamoto; Gary M Wessel
Journal:  Dev Biol       Date:  2013-01-25       Impact factor: 3.582

8.  Nanos functions to maintain the fate of the small micromere lineage in the sea urchin embryo.

Authors:  Celina E Juliano; Mamiko Yajima; Gary M Wessel
Journal:  Dev Biol       Date:  2009-10-28       Impact factor: 3.582

9.  Genome and epigenome engineering CRISPR toolkit for in vivo modulation of cis-regulatory interactions and gene expression in the chicken embryo.

Authors:  Ruth M Williams; Upeka Senanayake; Mara Artibani; Gunes Taylor; Daniel Wells; Ahmed Ashour Ahmed; Tatjana Sauka-Spengler
Journal:  Development       Date:  2018-02-23       Impact factor: 6.868

10.  Search-and-replace genome editing without double-strand breaks or donor DNA.

Authors:  Andrew V Anzalone; Peyton B Randolph; Jessie R Davis; Alexander A Sousa; Luke W Koblan; Jonathan M Levy; Peter J Chen; Christopher Wilson; Gregory A Newby; Aditya Raguram; David R Liu
Journal:  Nature       Date:  2019-10-21       Impact factor: 69.504

View more
  1 in total

1.  Distinct regulatory states control the elongation of individual skeletal rods in the sea urchin embryo.

Authors:  Kristina Tarsis; Tsvia Gildor; Miri Morgulis; Smadar Ben-Tabou de-Leon
Journal:  Dev Dyn       Date:  2022-04-22       Impact factor: 2.842

  1 in total

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