A2 Refereed review article in a scientific journal

CRISPR/Cas9 guided genome and epigenome engineering and its therapeutic applications in immune mediated diseases




AuthorsSingh D., Hawkins R., Lahesmaa R., Tripathi S.

PublisherElsevier Ltd

Publication year2019

JournalSeminars in Cell and Developmental Biology

Journal name in sourceSeminars in Cell and Developmental Biology

Volume96

First page 32

Last page43

DOIhttps://doi.org/10.1016/j.semcdb.2019.05.007

Web address https://doi.org/10.1016/j.semcdb.2019.05.007

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/41674143


Abstract

Recent developments in the nucleic acid editing technologies have provided a powerful tool to precisely engineer the genome and epigenome for studying many aspects of immune cell differentiation and development as well as several immune mediated diseases (IMDs) including autoimmunity and cancer. Here, we discuss the recent technological achievements of the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)-based RNA-guided genome and epigenome editing toolkit and provide an insight into how CRISPR/Cas9 (CRISPR Associated Protein 9) toolbox could be used to examine genetic and epigenetic mechanisms underlying IMDs. In addition, we will review the progress in CRISPR/Cas9-based genome-wide genome and epigenome screens in various cell types including immune cells. Finally, we will discuss the potential of CRISPR/Cas9 in defining the molecular function of disease associated SNPs overlapping gene regulatory elements.


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