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条件性Ppap2b/Lpp3无效等位基因的产生。

Generation of a conditional Ppap2b/Lpp3 null allele.

作者信息

Escalante-Alcalde Diana, Sánchez-Sánchez Roberto, Stewart Colin L

机构信息

Cancer and Developmental Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.

出版信息

Genesis. 2007 Jul;45(7):465-9. doi: 10.1002/dvg.20314.

Abstract

Lpp3, formerly known as Pap2b, is a lipid phosphohydrolase enzyme. Some of its substrates and products are lipids with potent biological and signaling activities such as phosphatidic acid, lysophosphatidic acid, sphingosine-1-phosphate, diacylglycerol, sphingosine, and ceramide. Lpp3 is dynamically expressed during development and is widely distributed in adult tissues. Targeted inactivation of Lpp3 gene (Ppap2b) in the mouse results in embryonic lethality because of defects in extraembryonic vascular development and gastrulation. To study the participation of Lpp3 later in development and in specific cell lineages we generated a conditional allele of Ppap2b. This was accomplished by flanking critical exons, responsible for its catalytic activity with loxP sites. A generalized Cre-mediated recombination of this allele yielded a phenotype fundamentally identical to our previously reported Ppap2b null allele.

摘要

Lpp3,以前称为Pap2b,是一种脂质磷酸水解酶。它的一些底物和产物是具有强大生物学和信号传导活性的脂质,如磷脂酸、溶血磷脂酸、鞘氨醇-1-磷酸、二酰基甘油、鞘氨醇和神经酰胺。Lpp3在发育过程中动态表达,广泛分布于成年组织中。在小鼠中靶向灭活Lpp3基因(Ppap2b)会导致胚胎致死,原因是胚外血管发育和原肠胚形成存在缺陷。为了研究Lpp3在发育后期和特定细胞谱系中的参与情况,我们构建了Ppap2b的条件等位基因。这是通过在负责其催化活性的关键外显子两侧侧翼插入loxP位点来实现的。该等位基因的普遍Cre介导重组产生的表型与我们之前报道的Ppap2b无效等位基因基本相同。

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