Gluten is an important protein source for human beings and a wide diversity of foods has been developed to take advantageof this protein in wheat flour. However, some individuals, suffering from Celiac Disease (CD), cannot tolerate proline andglutamine-rich gluten peptides including γ-gliadins. A life-long gluten free diet is the only known effective treatment forsuch patients. However, the sensitivity intension in CD patients can be controlled by RNA interference (RNAi) technology.The main aim of the present study is to develop an efficient and specific siRNA-inducing cassette, as a first and criticalstep for an effective targeting of mRNAs of wheat γ-gliadins. To achieve this aim, we have followed the strategy based on200 bp in sense and antisense orientation with the ~160bp sequence of none potent siRNA-containing region from γ-gliadin gene as a spacer in between. The endosperm-specific γ-gliadin promoter was sub-cloned into upstream the cassette.The nucleotide alignment results validated the sequence data of γ-gliadin promoter and the direct inserts with highhomology identities of 99% and 99.97%, respectively. Here, six potential and consecutively arranged-siRNA sites werepredicted using computational approaches. All of these sites covered the inverted repeats region with high efficacy andperformance values for triggering RNAi.