Precise in vivo functional analysis of DNA variants with base editing using ACEofBASEs target prediction

• Verfasst von: Cornean, Alex [VerfasserIn]
• Verfasst von: Gierten, Jakob [VerfasserIn]
• Verfasst von: Welz, Bettina [VerfasserIn]
• Verfasst von: Mateo, Juan L. [VerfasserIn]
• Verfasst von: Thumberger, Thomas [VerfasserIn]
• Verfasst von: Wittbrodt, Joachim [VerfasserIn]
• Titel: Precise in vivo functional analysis of DNA variants with base editing using ACEofBASEs target prediction
• Verf.angabe: authors: Alex Cornean, Jakob Gierten, Bettina Welz, Juan L. Mateo, Thomas Thumberger, Joachim Wittbrodt
• E-Jahr: 2021
• Jahr: July 26, 2021
• Umfang: 63 S.
• Illustrationen: Illustrationen
• Fussnoten: Gesehen am 27.02.2024
• Titel Quelle: Enthalten in: bioRxiv beta
• Ort Quelle: Cold Spring Harbor : Cold Spring Harbor Laboratory, NY, 2013
• Band/Heft Quelle: (2021) vom: Juli, Artikel-ID 2021.07.26.453883, Seite 1-63
• DOI: doi:10.1101/2021.07.26.453883
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1881666743

Abstract

Single nucleotide variants (SNVs) are prevalent genetic factors shaping individual trait profiles and disease susceptibility. The recent development and optimizations of base editors, rubber and pencil genome editing tools now promise to enable direct functional assessment of SNVs in model organisms. However, the lack of bioinformatic tools aiding target prediction limits the application of base editing in vivo. Here, we provide a framework for adenine and cytosine base editing in medaka (Oryzias latipes) and zebrafish (Danio rerio), ideal for scalable validation studies. We developed an online base editing tool ACEofBASEs (a careful evaluation of base-edits), to facilitate decision-making by streamlining sgRNA design and performing off-target evaluation. We used state-of-the-art adenine (ABE) and cytosine base editors (CBE) in medaka and zebrafish to edit eye pigmentation genes and transgenic GFP function with high efficiencies. Base editing in the genes encoding troponin T and the potassium channel ERG faithfully recreated known cardiac phenotypes. We finally validated missense mutations in novel candidate genes of congenital heart disease (CHD) dapk3, ube2b, usp44, and ptpn11 and present the resulting heart specific phenotypes. This base editing framework applies to a wide range of SNV-susceptible traits accessible in fish, facilitating straight-forward candidate validation and prioritization for detailed mechanistic downstream studies.