Generation and characterization of an estrogen receptor alpha-iCre knock-in mouse

被引：9
|
作者：
Park, Chan Jin [1 ]
Chen, Guanglin [1 ]
Koo, Yongbum [2 ]
Lin, Po-Ching P. [1 ]
Cacioppo, Joseph A. [1 ]
Prohaska, Hailey [1 ]
Ko, CheMyong J. [1 ]
机构：
[1] Univ Illinois, Coll Vet Med, Comparat Biosci, 3806 VMBSB,MC-002,2001 South Lincoln Ave, Urbana, IL 61801 USA
[2] Inje Univ, Sch Biol Sci, Gimhae, South Korea
来源：
GENESIS | 2017年 / 55卷 / 12期
关键词：
BAC clone; estrogen receptor alpha; iCre recombinase; transgenic; ESTRADIOL-MEDIATED PROTECTION; EARLY POSTNATAL-DEVELOPMENT; GENE-EXPRESSION; BRAIN-INJURY; HYPOTHALAMIC NEURONS; REPRODUCTIVE-TRACT; TRANSGENIC MICE; ER-ALPHA; BETA; CORTEX;
D O I：
10.1002/dvg.23084
中图分类号：
Q [生物科学];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
Two estrogen receptors, ESR1 and ESR2, are responsible for the classical actions of estrogens in mammalian species. They display different spatiotemporal expression patterns and nonoverlapping functions in various tissues and physiological conditions. In this study, a novel knock-in mouse line that expresses codon-improved Cre recombinase (iCre) under regulation of the natural Esr1 promoter (Esr1-iCre) was developed. Functional characterization of iCre expression by crossing them with reporter lines (ROSA26-lacZ or Ai9-RFP) showed that iCre is faithfully expressed in Esr1-lineage cells. This novel transgenic mouse line will be a useful animal model for lineage-tracing Esr1-expressing cells, selective gene ablation in the Esr1-lineage cells and for generating global Esr1 knockout mice.
引用
收藏
页数：11
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