Unknown

Dataset Information

0

Genome-wide Cas9-mediated screening of essential non-coding regulatory elements via libraries of paired single-guide RNAs.


ABSTRACT: The functions of non-coding regulatory elements (NCREs), which constitute a major fraction of the human genome, have not been systematically studied. Here we report a method involving libraries of paired single-guide RNAs targeting both ends of an NCRE as a screening system for the Cas9-mediated deletion of thousands of NCREs genome-wide to study their functions in distinct biological contexts. By using K562 and 293T cell lines and human embryonic stem cells, we show that NCREs can have redundant functions, and that many ultra-conserved elements have silencer activity and play essential roles in cell growth and in cellular responses to drugs (notably, the ultra-conserved element PAX6_Tarzan may be critical for heart development, as removing it from human embryonic stem cells led to defects in cardiomyocyte differentiation). The high-throughput screen, which is compatible with single-cell sequencing, may allow for the identification of druggable NCREs.

SUBMITTER: Li Y 

PROVIDER: S-EPMC11310080 | biostudies-literature | 2024 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Genome-wide Cas9-mediated screening of essential non-coding regulatory elements via libraries of paired single-guide RNAs.

Li Yufeng Y   Tan Minkang M   Akkari-Henić Almira A   Zhang Limin L   Kip Maarten M   Sun Shengnan S   Sepers Jorian J JJ   Xu Ningning N   Ariyurek Yavuz Y   Kloet Susan L SL   Davis Richard P RP   Mikkers Harald H   Gruber Joshua J JJ   Snyder Michael P MP   Li Xiao X   Pang Baoxu B  

Nature biomedical engineering 20240522 7


The functions of non-coding regulatory elements (NCREs), which constitute a major fraction of the human genome, have not been systematically studied. Here we report a method involving libraries of paired single-guide RNAs targeting both ends of an NCRE as a screening system for the Cas9-mediated deletion of thousands of NCREs genome-wide to study their functions in distinct biological contexts. By using K562 and 293T cell lines and human embryonic stem cells, we show that NCREs can have redundan  ...[more]

Similar Datasets

| S-EPMC5592164 | biostudies-literature
| S-EPMC9137126 | biostudies-literature
| S-EPMC8026597 | biostudies-literature
2024-01-28 | GSE254241 | GEO
| S-EPMC6731277 | biostudies-literature
| S-EPMC5333799 | biostudies-literature
| S-EPMC4544769 | biostudies-literature
| S-EPMC4446435 | biostudies-literature
| S-EPMC7065968 | biostudies-literature
| S-EPMC6023836 | biostudies-literature