PIWI-interacting RNAs (piRNAs) are one of three main classes of recently discovered small non-coding RNAs, alongside microRNAs and long non-coding RNAs. PiRNAs are transcribed from transposable elements and piRNA clusters. They play an important role in silencing these elements in germline and stem cells to maintain genomic stability, regulate gene expression, and support male germ cell development. Dysregulation of piRNAs has been linked to diseases such as cancer and male infertility. Despite their importance, piRNA biosynthesis remains poorly understood, especially the regulatory factors crafting their biogenesis. To study piRNA biosynthesis, we will use the C.Elegans model, since piRNAs are best characterized in C.Elegans and Drosophila, and many of their functions and genetic makeup is similar to that of humans. To learn about piRNA biosynthesis, it is essential to learn about CMTR-1 and CMTR-2, cap-methyltransferases involved in RNA capping process which will contribute in discovering a more detailed pathway of piRNNA biosynthesis. Our technique revolves around inserting Degron system tags into C.Elegans using CRISPR-Cas9, which will create a partially knockout CMTR-1 or CMTR-2 mutant strains These mutants will only be fully depleted of CMTR-1 or CMTR-2 when C. elegans is grown under KNAA conditions. After screening for homologous mutant-tagged CMTR-1 or CMTR-2, we will extract the piRNA population and use next-generation sequencing to compare piRNA levels in CMTR-1 and CMTR-2 mutants with those in wild-type CMTR-1 and CMTR-2. By comparing piRNA abundants between CMTR-1 and CMTR-2 mutants and wild-type worms, we aim to unravel how RNA capping enzymes contribute to the control of biosynthesis of C.Elegans.