Identification of a zebrafish sat1 .a mutant
10.3969/j.issn.1005-4847.2016.06.001
- VernacularTitle:斑马鱼sat1．a突变体的鉴定
- Author:
Chuanlu WAN
;
Yifang YAN
;
Peng WANG
;
Yu LIN
;
Yu CAO
;
Qiang WANG
- Keywords:
Zebrafish;
Tol2 transposon;
sat1.a;
Nervous system;
in situ hybridization
- From:
Acta Laboratorium Animalis Scientia Sinica
2016;24(6):551-557
- CountryChina
- Language:Chinese
-
Abstract:
Objective In our previous study, we had generated various zebrafish mutant lines with tissue?specific GFP expression by Tol2 transposon?mediated insertional mutagenesis. Among these mutants,the Tol2:20141221t line ex?presses GFP in nervous system, while the position within zebrafish genome where transposon inserted has not yet been iden?tified. The aim of this study was to identify and analyze this genetically modified mutant. Methods The transgenic inser?tion loci in the genome of Tol2:20141221t line was identified byTAIL?PCR and the spatial and temporal expression profile of the affected gene was examined by in situ hybridization. Homozygous mutant of Tol2:20141221t was generated for explo?ring related developmental defects. Results Tol2 transposon was inserted into the 8th intron region of sat1.a gene, and in?duced premature transcription termination. The maternal and zygotic mutants of Tol2:20141221t was generated, while with?out apparent developmental defects. Conclusions We have generated and identified the zebrafishsat1.a mutant mediated by Tol2 transposon. This gene insertion mutant exhibits no obvious developmental abnormalities, but may serve as a power?ful tool to study the development of nervous system.
