A suite of new Dre recombinase drivers markedly expands the ability to perform intersectional genetic targeting

生物 重组酶 PDGFRA公司 Cre重组酶 命运图 Cre-Lox重组 祖细胞 转基因 计算生物学 细胞生物学 遗传学 转基因小鼠 干细胞 基因 癌症研究 重组 间质细胞 主旨
作者
Ximeng Han,Zhenqian Zhang,Lingjuan He,Huan Zhu,Yan Li,Wenjuan Pu,Maoying Han,Huan Zhao,Kuo Liu,Yi Li,Xiuzhen Huang,Mingjun Zhang,Hengwei Jin,Zan Lv,Juan Tang,Jinjin Wang,Ruilin Sun,Jian Fei,Xueying Tian,Sheng‐Zhong Duan
出处
期刊:Cell Stem Cell [Elsevier]
卷期号:28 (6): 1160-1176.e7 被引量:104
标识
DOI:10.1016/j.stem.2021.01.007
摘要

The use of the dual recombinase-mediated intersectional genetic approach involving Cre-loxP and Dre-rox has significantly enhanced the precision of in vivo lineage tracing, as well as gene manipulation. However, this approach is limited by the small number of Dre recombinase driver constructs available. Here, we developed more than 70 new intersectional drivers to better target diverse cell lineages. To highlight their applicability, we used these new tools to study the in vivo adipogenic fate of perivascular progenitors, which revealed that PDGFRa+ but not PDGFRa–PDGFRb+ perivascular cells are the endogenous progenitors of adult adipocytes. In addition to lineage tracing, we used members of this new suite of drivers to more specifically knock out genes in complex tissues, such as white adipocytes and lymphatic vessels, that heretofore cannot be selectively targeted by conventional Cre drivers alone. In summary, these new transgenic tools expand the intersectional genetic approach while enhancing its precision.

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