CRISPR/Cas in Echinoderms: Difference between revisions

From EchinoWiki
Jump to navigation Jump to search
imported>Ctelmer
No edit summary
imported>Ctelmer
No edit summary
Line 22: Line 22:
'''Editing other echinoderm species'''
'''Editing other echinoderm species'''


Editing technology has also been used in ''Hemicentrotus pulcherrimus'' ([https://www.echinobase.org/literature/article.do?method=display&articleId=47348 Liu et al. 2019]; [https://www.echinobase.org/literature/article.do?method=display&articleId=48597 Wessel et al. 2020]) and ''Temnopleurus reevesii'' (Yaguchi et al. 2020).
Editing technology has also been used in ''Hemicentrotus pulcherrimus'' ([https://www.echinobase.org/literature/article.do?method=display&articleId=47348 Liu et al. 2019]; [https://www.echinobase.org/literature/article.do?method=display&articleId=48597 Wessel et al. 2020]) and ''Temnopleurus reevesii'' ([https://www.echinobase.org/literature/article.do?method=display&articleId=48853 Yaguchi et al. 2020]).

Revision as of 10:01, 1 December 2020

Welcome to the Echinobase CRISPR/Cas resource. A brief literature and method review is followed by tables of gRNA spacer sequences.

Updated December 2020


S. purpuratus genome editing to create insertions and deletions

To date CRISPR/Cas9 has been used to introduce insertion and deletion mutations (indels) into S. purpuratus nodall (Lin and Su 2016), polyketide synthase 1, gcml (Oulhen and Wessel 2016), nanos2l (Oulhen et al. 2017) and dll1 (delta) (Mellott et al. 2017) genes. Attempts to mutate foxy (Oulhen et al. 2019) were unsuccessful. A number of different methods were used for gRNA synthesis (several using pT7-gRNA) and NLS-SpCas9-NLS (pCS2-nCas9n (zebrafish codon-optimized), or pCS2-3xFLAG-NLS-SpCas9-NLS (codon optimized for human with a 3XFLAG-tag) were used in these studies (see below for details). The gRNAs and mRNAs were microinjected into fertilized eggs.


Single nucleotide edits

Additional studies fused a deaminase to two mutants of SpCas9 for achieving targeted, single nucleotide edits to alx1, segment polarity protein dishevelled homolog DVL-3 (Dsh) and polyketide synthase 1 (Pks1) to produce STOP codons (Shevidi et al. 2017).


Reviews

Reviews of the methods are available (Cui et al. 2017; Lin et al. 2019).


Editing other echinoderm species

Editing technology has also been used in Hemicentrotus pulcherrimus (Liu et al. 2019; Wessel et al. 2020) and Temnopleurus reevesii (Yaguchi et al. 2020).