Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl
Preferences help
enabled [disable] Abstract
Number of results

Results found: 1

Number of results on page
first rewind previous Page / 1 next fast forward last

Search results

help Sort By:

help Limit search:
first rewind previous Page / 1 next fast forward last
EN
Advances in CRISPR-based editing and chimeric antigen receptor (CAR) T-cell engineering have pushed modern biomedical research into practical, high-impact space. This study reports a workshop-based investigation that applied CRISPR guideRNA design and promoter analysis methods routinely used in CAR T-cell design to the doublesex (dsx) gene of Anopheles gambiae. Using Ensembl and NCBI resources, multiple sequence alignment across Anopheles species and motif searches in the upstream region of dsx were performed to identify conserved target windows and a putative upstream regulatory region. The intron – exon boundary targeted by contemporary gene-drive strategies (intron4–exon5) proved highly conserved across sampled species, supporting its suitability for CRISPR targeting. A candidate promoter motif architecture, including a predicted TATA box and initiator element within a conserved upstream window, is presented as a putative regulatory locus for further experimental validation. The paper situates these findings in two applied contexts: precision promoter selection for CAR expression in therapeutic cell engineering, and CRISPR-driven mosquito population control with potential to reduce malaria burden in Nigeria. Limitations and ethical considerations are discussed with emphasis on the need for local, experimental follow-up.
first rewind previous Page / 1 next fast forward last
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.