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鸡δ1-晶体蛋白增强子在小鼠中的晶状体特异性活性。

Lens-specific activity of the chicken delta 1-crystallin enhancer in the mouse.

作者信息

Takahashi Y, Hanaoka K, Goto K, Kondoh H

机构信息

Department of Biosciences, School of Science, Kitasato University, Kanagawa, Japan.

出版信息

Int J Dev Biol. 1994 Jun;38(2):365-8.

PMID:7981046
Abstract

A lens-specific enhancer was identified in the third intron of the chicken delta 1-crystallin gene by analysis based on transient transfection of primary-cultured cells. To assess the significance of this enhancer's activity in embryonic lens cells during development, tkCAT gene carrying the enhancer was introduced into mouse embryos utilizing ES (embryonic stem) cell-mediated gene transfer. In the undifferentiated culture condition, ES lines with enhancer-carrying tkCAT did not express any significant level of CAT (chloramphenicol acetyltransferase). However, when the ES cells were injected into a blastocyst and allowed to differentiate into various somatic cells of an embryo, CAT expression was observed exclusively in lens, and the expression was dependent upon the delta 1-crystallin enhancer. We concluded that the delta 1-crystallin enhancer alone is sufficient for eliciting lens-specific gene expression in developing mouse embryos and that the mechanism of lens-specific regulation effected by the delta 1-crystallin enhancer is conserved between the chicken and the mouse.

摘要

通过对原代培养细胞进行瞬时转染分析,在鸡δ1-晶状体蛋白基因的第三个内含子中鉴定出了一个晶状体特异性增强子。为了评估该增强子在胚胎发育过程中对胚胎晶状体细胞活性的重要性,利用胚胎干细胞(ES)介导的基因转移技术,将携带该增强子的tkCAT基因导入小鼠胚胎。在未分化的培养条件下,携带增强子的tkCAT的ES细胞系未表达任何显著水平的氯霉素乙酰转移酶(CAT)。然而,当将ES细胞注射到囊胚中并使其分化为胚胎的各种体细胞时,仅在晶状体中观察到了CAT表达,且该表达依赖于δ1-晶状体蛋白增强子。我们得出结论,单独的δ1-晶状体蛋白增强子足以在发育中的小鼠胚胎中引发晶状体特异性基因表达,并且由δ1-晶状体蛋白增强子实现的晶状体特异性调控机制在鸡和小鼠之间是保守的。

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