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肠道富集型克勒普样因子基因在发育及肠道肿瘤发生过程中的表达

Expression of the gut-enriched Krüppel-like factor gene during development and intestinal tumorigenesis.

作者信息

Ton-That H, Kaestner K H, Shields J M, Mahatanankoon C S, Yang V W

机构信息

Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

FEBS Lett. 1997 Dec 15;419(2-3):239-43. doi: 10.1016/s0014-5793(97)01465-8.

Abstract

We examined the expression of GKLF (gut-enriched Krüppel-like factor), a recently identified zinc finger-containing transcription factor, in mice during development using the ribonuclease protection assay. In the adult, the level of GKLF transcript is abundant throughout the gastrointestinal tract. Between embryonic days 10 and 19 (E10 and E19) of development, the initial level of whole embryo GKLF transcript is low but begins to rise on E13 and peaks on E17. In the newborn, GKLF transcript level is higher in the colon than in the small intestine although the levels in both organs rise with increasing age. Expression of GKLF was also examined in the intestinal tract of the Min mouse, a model of intestinal tumorigenesis. The level of GKLF transcript is significantly decreased in the intestine of Min mice during a period of tumor formation when compared to age-matched control littermates. Our findings indicate that GKLF expression correlates with certain periods of gut development and is down-regulated during intestinal tumorigenesis, suggesting that GKLF may play a role in gut development and/or tumor formation.

摘要

我们使用核糖核酸酶保护试验检测了一种最近鉴定出的含锌指转录因子——肠富集型Krüppel样因子(GKLF)在小鼠发育过程中的表达情况。在成年小鼠中,GKLF转录本水平在整个胃肠道中都很丰富。在胚胎发育的第10天到第19天(E10和E19)之间,全胚胎GKLF转录本的初始水平较低,但在E13时开始上升,并在E17时达到峰值。在新生小鼠中,结肠中的GKLF转录本水平高于小肠,尽管两个器官中的水平都随着年龄的增长而升高。我们还在肠道肿瘤发生模型Min小鼠的肠道中检测了GKLF的表达。与年龄匹配的对照同窝小鼠相比,在肿瘤形成期间,Min小鼠肠道中GKLF转录本水平显著降低。我们的研究结果表明,GKLF表达与肠道发育的某些时期相关,并且在肠道肿瘤发生过程中被下调,这表明GKLF可能在肠道发育和/或肿瘤形成中发挥作用。

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