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.

Guardado en:
Detalles Bibliográficos
Autores principales: 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
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2019
Materias:
Q
Acceso en línea:https://doaj.org/article/370492b1e1f04ee38f9a459c9cce9e77
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:370492b1e1f04ee38f9a459c9cce9e77
record_format dspace
spelling oai:doaj.org-article:370492b1e1f04ee38f9a459c9cce9e772021-12-02T17:01:50ZCRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation10.1038/s41467-019-12028-52041-1723https://doaj.org/article/370492b1e1f04ee38f9a459c9cce9e772019-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-12028-5https://doaj.org/toc/2041-1723CRISPR-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.Rubina TuladharYunku YeuJohn Tyler PiazzaZhen TanJean Rene ClemenceauXiaofeng WuQuinn BarrettJeremiah HerbertDavid H. MathewsJames KimTae Hyun HwangLawrence LumNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
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
CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
description 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.
format article
author 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
author_facet 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
author_sort Rubina Tuladhar
title CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
title_short CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
title_full CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
title_fullStr CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
title_full_unstemmed CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
title_sort crispr-cas9-based mutagenesis frequently provokes on-target mrna misregulation
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/370492b1e1f04ee38f9a459c9cce9e77
work_keys_str_mv AT rubinatuladhar crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT yunkuyeu crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT johntylerpiazza crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT zhentan crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT jeanreneclemenceau crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT xiaofengwu crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT quinnbarrett crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT jeremiahherbert crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT davidhmathews crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT jameskim crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT taehyunhwang crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
AT lawrencelum crisprcas9basedmutagenesisfrequentlyprovokesontargetmrnamisregulation
_version_ 1718382019947266048