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人类白细胞整合素CD11a启动子指导转基因小鼠白细胞中的表达。

The human leukocyte integrin CD11a promoter directs expression in leukocytes of transgenic mice.

作者信息

Ritchie K A, Aprikian A, Gollahon K A, Hickstein D D

机构信息

Medical Research Service, Seattle Veterans Affairs Medical Center, WA 98108, USA.

出版信息

Blood. 1995 Jul 1;86(1):147-55.

PMID:7795220
Abstract

The human CD11a molecule is expressed specifically on lymphocytes, monocyte/macrophages, and neutrophils, in which it mediates important adhesion-related functions. We used 1.7 kb of regulatory sequences upstream from the human CD11a gene transcription start site to drive expression of a modified human CD4 reporter gene in transgenic mice. The transgene was expressed in a tissue-specific fashion on all leukocytes and paralleled endogenous mouse CD11a expression. All five founder mice expressed the transgene, providing evidence for integration site-independent expression. However, expression was not proportional to transgene copy number. These studies indicate that (1) the mutated human CD4 serves as an excellent reporter for analysis of leukocyte-specific promoters; (2) the CD11a regulatory unit used here represents a novel reagent for targeting gene expression to leukocytes; and (3) additional regulatory regions will be required for copy-number-dependent activity of CD11a regulatory sequences.

摘要

人类CD11a分子特异性表达于淋巴细胞、单核细胞/巨噬细胞和中性粒细胞上,在这些细胞中它介导重要的黏附相关功能。我们使用人类CD11a基因转录起始位点上游1.7 kb的调控序列,驱动修饰后的人类CD4报告基因在转基因小鼠中表达。转基因以组织特异性方式在所有白细胞上表达,并与内源性小鼠CD11a表达平行。所有五只奠基小鼠均表达转基因,为整合位点非依赖性表达提供了证据。然而,表达与转基因拷贝数不成比例。这些研究表明:(1)突变的人类CD4可作为分析白细胞特异性启动子的优良报告基因;(2)此处使用的CD11a调控单元是一种将基因表达靶向白细胞的新型试剂;(3)CD11a调控序列的拷贝数依赖性活性还需要其他调控区域。

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