Regulation of Gene Expression in the Intestinal Epithelium

被引:28
|
作者
Richmond, Camilla A. [1 ]
Breault, David T. [2 ]
机构
[1] Harvard Univ, Sch Med, Childrens Hosp Boston, Div Gastroenterol, Boston, MA 02163 USA
[2] Harvard Univ, Sch Med, Childrens Hosp Boston, Div Endocrinol, Boston, MA USA
关键词
SERINE-THREONINE KINASE; SECRETORY-CELL LINEAGE; NUCLEAR FACTOR 1-ALPHA; MOUSE SMALL-INTESTINE; CDX2 MUTANT MICE; STEM-CELLS; TRANSCRIPTION FACTORS; COLORECTAL-CANCER; BETA-CATENIN; JUVENILE POLYPOSIS;
D O I
10.1016/S1877-1173(10)96009-2
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
Regulation of gene expression within the intestinal epithelium is complex and controlled by various signaling pathways that regulate the balance between proliferation and differentiation. Proliferation is required both to grow and to replace cells lost through apoptosis and attrition, yet in all but a few cells, differentiation must take place to prevent uncontrolled growth (cancer) and to provide essential functions. In this chapter, we review the major signaling pathways underlying regulation of gene expression within the intestinal epithelium, based primarily on data from mouse models, as well as specific morphogens and transcription factor families that have a major role in regulating intestinal gene expression, including the Hedgehog family, Forkhead Box (FOX) factors, Homeobox (HOX) genes, ParaHox genes, GATA transcription factors, canonical Wnt/beta-catenin signaling, EPH/Ephrins, Sox9, BMP signaling, PTEN/PI3K, LKB1, K-RAS, Notch pathway, HNF, and MATH1. We also briefly highlight important emerging areas of gene regulation, including microRNA (miRNA) and epigenetic regulation.
引用
收藏
页码:207 / 229
页数:23
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