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. 2021 Jan 20;217(3):iyab006. doi: 10.1093/genetics/iyab006

Table 1.

Plasmids to support generation of new TIR1 alleles and other transgenes at standardized genetic loci through CRISPR/Cas-based genome editing

Plasmid name Description Purpose
pJW1838 SapTrap sgRNA (F + E) vector, K09B11.2 U6 promoter and 3'UTR Creating new sgRNA (F + E) plasmids)
pJW1839 SapTrap sgRNA (F + E) vector, R07E5.16 U6 promoter Creating new sgRNA (F + E) plasmids)
pJW1836 promoterless SV40 NLS::mScarlet-I (dpi)::PEST::tbb-2 3'UTR vector Promoter reporter, test new tissue-specific promoters
pJW1841 promoterless SV40 NLS::mScarlet-I (dpi)::tbb-2 3'UTR vector Promoter reporter, test new tissue-specific promoters
pJW1849 ttTi4348 site targeting sgRNA (F + E) with K09B11.2 U6 promoter and 3'UTR CRISPR/Cas9 editing of ttTi4348 insertion site
pJW1850 ttTi5605 site targeting sgRNA (F + E) with K09B11.2 U6 promoter and 3'UTR CRISPR/Cas9 editing of ttTi5605 insertion site
pJW1851 cxTi10882 site targeting sgRNA (F + E) with K09B11.2 U6 promoter and 3'UTR CRISPR/Cas9 editing of cxTi10882 insertion site
pJW1882 ttTi4348 site targeting sgRNA (F + E) with R07E5.16 U6 promoter and 3'UTR CRISPR/Cas9 editing of ttTi4348 insertion site
pJW1883 ttTi5605 site targeting sgRNA (F + E) with R07E5.16 U6 promoter and 3'UTR CRISPR/Cas9 editing of ttTi5605 insertion site
pJW1884 cxTi10882 site targeting sgRNA (F + E) with R07E5.16 U6 promoter and 3'UTR CRISPR/Cas9 editing of cxTi10882 insertion site
pJW1947 pes-10Δ minimal promoter::SV40 NLS::mScarlet-I (dpi)::tbb-2 3'UTR vector Promoter reporter, test new tissue-specific enhancers
pJW1948 pes-10Δ minimal promoter::SV40 NLS::mScarlet-I (dpi)::PEST::tbb-2 3'UTR vector Promoter reporter, test new tissue-specific enhancers
pTD77 eft-3p::Cas9, R07E5.16 U6::sgRNA targeting LGI site where ttTi4348 Mos is inserted CRISPR/Cas9 editing of ttTi4348 insertion site
pTD78 eft-3p::Cas9, R07E5.16 U6::sgRNA targeting LGII site where ttTi5605 Mos is inserted CRISPR/Cas9 editing of ttTi5605 insertion site