Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.1.26.4 (
RNase H
)
2,751
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
MRP
RNA is an abundant, essential noncoding RNA whose functions have been proposed in yeast but are incompletely understood in humans. Mutations in the genomic locus for
MRP
RNA cause pleiotropic human diseases, including cartilage hair hypoplasia (CHH). Here we applied CRISPR-Cas9 genome editing to disrupt the endogenous human
MRP
RNA locus, thereby attaining what has eluded RNAi and
RNase H
experiments: elimination of
MRP
RNA in the majority of cells. The resulting accumulation of ribosomal RNA (rRNA) precursor-analyzed by RNA fluorescent in situ hybridization (FISH), Northern blots, and RNA sequencing-implicates
MRP
RNA in pre-rRNA processing. Amelioration of pre-rRNA imbalance is achieved through rescue of
MRP
RNA levels by ectopic expression. Furthermore, affinity-purified
MRP
ribonucleoprotein (RNP) from HeLa cells cleaves the human pre-rRNA in vitro at at least one site used in cells, while RNP isolated from cells with CRISPR-edited
MRP
loci loses this activity, and ectopic
MRP
RNA expression restores cleavage activity. Thus, a role for RNase
MRP
in human pre-rRNA processing is established. As demonstrated here, targeted CRISPR disruption is a valuable tool for functional studies of essential noncoding RNAs that are resistant to RNAi and
RNase H
-based degradation.
...
PMID:Targeted CRISPR disruption reveals a role for RNase MRP RNA in human preribosomal RNA processing. 2811 65