Products/Services Used | Details | Operation |
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Gene Synthesis> | To test the expression competence of the cloned bu7SK and buU6 promoters, the pMCS-shEGFP and pMCS-sh1864 base vectors were constructed from pMD18T by ligating a 65 bp synthetic copy of an EGFP-specific shRNA or a control scrambled shRNA (Addgene plasmid #1864; Raleigh, NC, USA) sequence produced by chemical synthesis (GenScript, Nanjing, China) between the BamHI and HindIII sites (Takara, Dalian, China), respectively. Then anti-EGFP shRNA expression cassettes bu7SK-shEGFP and buU6-shEGFP were constructed by ligating bu7SK and buU6 into pMCS-shEGFP, respectively. | Get A Quote |
RNA polymerase III (pol III) type 3 promoters, such as 7SK and U6, are routinely used to induce short hairpin RNAs (shRNAs) to knockdown gene expression by RNA interference (RNAi). To extend the application of RNAi to studies of buffalo, an shRNAs expressing system using the buffalo pol III promoters was developed. Buffalo 7SK promoter (bu7SK) and U6 promoter (buU6) sequences upstream of the full-length 7SK and U6 small nuclear RNA sequence in the buffalo genome were identified and characterized, respectively. To determine the functionality of these promoters in constructs driving shRNA expression, anti-EGFP shRNAs (shEGFP) cassettes under the direction of bu7SK and buU6 were constructed. We further c... More