Literature DB >> 32550459

An isoform-specific allele of the sax-7 locus.

Dylan Rahe1, Ines Carrera2,3, Filip Cosmanescu2, Oliver Hobert1,2.   

Abstract

Entities:  

Year:  2019        PMID: 32550459      PMCID: PMC7252388          DOI: 10.17912/micropub.biology.000092

Source DB:  PubMed          Journal:  MicroPubl Biol        ISSN: 2578-9430


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is a novel isoform-specific allele of the A. sax-7 locus encodes two isoforms of an L1CAM homolog. Existing null alleles affect either the long isoform (nj53) or both isoforms (nj48, ky146, and dz156). ot820 is a short deletion mutant that affects only the short isoform. B. sgRNA targets the beginning of the first exon of sax-7S, and ot820 is a 8bp deletion 15bp from the start codon.

Description

The immunoglobulin superfamily member sax-7 produces a long and short isoform that appear to have distinct functions (Chen et al. 2001; Wang et al. 2005; Sasakura et al. 2005; Pocock et al. 2008). An isoform-specific allele for the long isoform, sax-7L, was previously reported (Sasakura et al. 2005), but an isoform-specific allele for the short isoform, sax-7S, has been lacking (Fig. 1A). We used CRISPR/Cas9 to generate such an allele, using the unc-22 co-CRISPR method (Kim et al. 2014). The ot820 allele was isolated using sgRNA targeted to the first exon of sax-7S (sgRNA sequece: 5’ – TGGGGTTACGAGAGACGAT – 3’). Twitching progeny were screened by PCR and Sanger sequencing, and an 8bp deletion 15bp from the start codon was isolated (screening primers: 5’ – GGTGCTTCTCTGGTGGTAGC – 3’ and 5’ – TGTTGGCAAACAAAATACACG – 3’, Fig. 1B). While the sax-7L isoform is predicted to be entirely unaffected by this allele, the resultant frameshift is predicted to generate a 49 amino acid protein in which all but the first five amino acids of sax-7S are aberrant and has no predicted signal sequence, before terminating in a premature stop in the second exon (Fig. 1B). This allele therefore likely represents a null for the sax-7S isoform. After we generated this allele, a recent paper reported an additional sax-7S-specific allele, with somewhat similar, but not identical sequence properties (Chen et al., 2019). Consistent with previous evidence of distinct functions of sax-7 isoforms, these authors showed differing axon fasciculation defects between these two alleles, which is further distinct from a total null allele. These new sax-7S alleles should help to reveal new insights into the role of L1CAM/SAX-7 isoforms in the nervous system.

Reagents

OH13830 sax-7(ot820) IV; oyIs14 V. Will be available at CGC.
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