PUBLICATION

Expansion of CRISPR/Cas9 genome targeting sites in zebrafish by Csy4-based RNA processing

Authors
Qin, W., Liang, F., Feng, Y., Bai, H., Yan, R., Li, S., Lin, S.
ID
ZDB-PUB-150805-9
Date
2015
Source
Cell Research   25(9): 1074-7 (Journal)
Registered Authors
Qing, Wei
Keywords
none
MeSH Terms
  • Animals
  • Base Sequence
  • Binding Sites
  • CRISPR-Cas Systems/genetics*
  • Genome*
  • Monophenol Monooxygenase/genetics
  • Monophenol Monooxygenase/metabolism
  • RNA, Guide, Kinetoplastida/metabolism*
  • Zebrafish/genetics*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed
26238401 Full text @ Cell Res.
Abstract
With its advantages of simple design and cost-efficiency, the CRISPR/Cas9 technology has been widely adapted for genome editing in different species including zebrafish1. In zebrafish studies, guide RNA (gRNA) is usually produced via in vitro transcription followed by microinjection with Cas9 mRNA into embryos.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping