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

被引:94
作者
Ton-That, H
Kaestner, KH
Shields, JM
Mahatanankoon, CS
Yang, VW
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[3] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
关键词
gut-enriched Kruppel-like factor; gastrointestinal tract; development; tumorigenesis; Min mouse; ribonuclease protection assay;
D O I
10.1016/S0014-5793(97)01465-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We examined the expression of GKLF (gut-enriched Kruppel-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,vith 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. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:239 / 243
页数:5
相关论文
共 26 条
  • [1] ANDERSON KP, 1995, MOL CELL BIOL, V15, P5957
  • [2] BURT RW, 1992, GENETIC BASIS COMMON, P650
  • [3] Bussey HJR., 1975, Familial polyposis coli: family studies, histopathology, differential diagnosis and results of treatment
  • [4] MIGRATION OF FETAL INTESTINAL INTERVILLOUS CELLS IN NEONATAL MICE
    CALVERT, R
    POTHIER, P
    [J]. ANATOMICAL RECORD, 1990, 227 (02): : 199 - 206
  • [5] Homeosis and intestinal tumours in Cdx2 mutant mice
    Chawengsaksophak, K
    James, R
    Hammond, VE
    Kontgen, F
    Beck, F
    [J]. NATURE, 1997, 386 (6620) : 84 - 87
  • [6] GENETIC IDENTIFICATION OF MOM-1, A MAJOR MODIFIER LOCUS AFFECTING MIN-INDUCED INTESTINAL NEOPLASIA IN THE MOUSE
    DIETRICH, WF
    LANDER, ES
    SMITH, JS
    MOSER, AR
    GOULD, KA
    LUONGO, C
    BORENSTEIN, N
    DOVE, W
    [J]. CELL, 1993, 75 (04) : 631 - 639
  • [7] EE HC, 1995, AM J PATHOL, V147, P586
  • [8] A gene for a novel zinc-finger protein expressed in differentiated epithelial cells and transiently in certain mesenchymal cells
    GarrettSinha, LA
    Eberspaecher, H
    Seldin, MF
    deCrombrugghe, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (49) : 31384 - 31390
  • [9] DIFFERENTIATION AND SELF-RENEWAL IN THE MOUSE GASTROINTESTINAL EPITHELIUM
    GORDON, JI
    HERMISTON, ML
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (06) : 795 - 803
  • [10] HENNING SJ, 1985, ANNU REV PHYSIOL, V47, P231