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表达捕获:通过胚胎干细胞中的基因捕获鉴定在造血和内皮谱系中表达的新基因。

Expression trapping: identification of novel genes expressed in hematopoietic and endothelial lineages by gene trapping in ES cells.

作者信息

Stanford W L, Caruana G, Vallis K A, Inamdar M, Hidaka M, Bautch V L, Bernstein A

机构信息

Program in Molecular Biology and Cancer, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.

出版信息

Blood. 1998 Dec 15;92(12):4622-31.

PMID:9845528
Abstract

We have developed a large-scale, expression-based gene trap strategy to perform genome-wide functional analysis of the murine hematopoietic and vascular systems. Using two different gene trap vectors, we have isolated embryonic stem (ES) cell clones containing lacZ reporter gene insertions in genes expressed in blood island and vascular cells, muscle, stromal cells, and unknown cell types. Of 79 clones demonstrating specific expression patterns, 49% and 16% were preferentially expressed in blood islands and/or the vasculature, respectively. The majority of ES clones that expressed lacZ in blood islands also expressed lacZ upon differentiation into hematopoietic cells on OP9 stromal layers. Importantly, the in vivo expression of the lacZ fusion products accurately recapitulated the observed in vitro expression patterns. Expression and sequence analysis of representative clones suggest that this approach will be useful for identifying and mutating novel genes expressed in the developing hematopoietic and vascular systems.

摘要

我们开发了一种基于表达的大规模基因捕获策略,用于对小鼠造血和血管系统进行全基因组功能分析。使用两种不同的基因捕获载体,我们分离出了胚胎干细胞(ES)克隆,这些克隆在血岛、血管细胞、肌肉、基质细胞和未知细胞类型中表达的基因中插入了lacZ报告基因。在79个显示特定表达模式的克隆中,分别有49%和16%在血岛和/或脉管系统中优先表达。大多数在血岛中表达lacZ的ES克隆在分化为OP9基质层上的造血细胞时也表达lacZ。重要的是,lacZ融合产物的体内表达准确地重现了观察到的体外表达模式。对代表性克隆的表达和序列分析表明,这种方法将有助于鉴定和突变在发育中的造血和血管系统中表达的新基因。

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