Modeling a human CLP1 mutation in mouse identifies an accumulation of tyrosine pre-tRNA fragments causing pontocerebellar hypoplasia type 10-Reference-Cited by-同舟云学术

Modeling a human CLP1 mutation in mouse identifies an accumulation of tyrosine pre-tRNA fragments causing pontocerebellar hypoplasia type 10

Published:2021-09 Issue: Volume:570 Page:60-66
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Morisaki Ikuko,Shiraishi Hiroshi,Fujinami Hiroyuki,Shimizu Nobuyuki,Hikida Takatoshi,Arai Yuji,Kobayashi Takashi,Hanada Reiko^ORCID,Penninger Josef M.,Fujiki Minoru,Hanada Toshikatsu^ORCID

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference23 articles.

1. The human RNA kinase hClp1 is active on 3′ transfer RNA exons and short interfering RNAs;Weitzer;Nature,2007

2. hClp1: a novel kinase revitalizes RNA metabolism;Weitzer;Cell Cycle,2007

3. Human RNA 5′-kinase (hClp1) can function as a tRNA splicing enzyme in vivo;Ramirez;RNA,2008

4. Characterization of a thermostable archaeal polynucleotide kinase homologous to human Clp1;Jain;RNA,2009

5. CLP1 acts as the main RNA kinase in mice;Fujinami;Biochem. Biophys. Res. Commun.,2020

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