CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
CRISPR-Cas9 genome editing is presumed to knock out gene function by generating a frameshift during NHEJ repair. Here, the authors investigate mRNA and protein expression in edited lines and find genome editing can generate internal ribosome entry sites or alternatively spliced variants.
Enregistré dans:
Auteurs principaux: | Rubina Tuladhar, Yunku Yeu, John Tyler Piazza, Zhen Tan, Jean Rene Clemenceau, Xiaofeng Wu, Quinn Barrett, Jeremiah Herbert, David H. Mathews, James Kim, Tae Hyun Hwang, Lawrence Lum |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2019
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/370492b1e1f04ee38f9a459c9cce9e77 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Conceptual modeling of mRNA decay provokes new hypotheses.
par: Judith Somekh, et autres
Publié: (2014) -
A splice mutation and mRNA decay of EXT2 provoke hereditary multiple exostoses.
par: Chen Tian, et autres
Publié: (2014) -
Small genomic insertions form enhancers that misregulate oncogenes
par: Brian J. Abraham, et autres
Publié: (2017) -
Correction: Corrigendum: Small genomic insertions form enhancers that misregulate oncogenes
par: Brian J. Abraham, et autres
Publié: (2017) -
Misregulation of Wnt Signaling Pathways at the Plasma Membrane in Brain and Metabolic Diseases
par: Mustafa Karabicici, et autres
Publié: (2021)