Epigenetic regulation of intestinal stem cell differentiation

被引:10
|
作者
Verzi, Michael P. [1 ,2 ,3 ]
Shivdasani, Ramesh A. [4 ,5 ,6 ,7 ,8 ]
机构
[1] Rutgers State Univ, Dept Genet, Piscataway, NJ 08854 USA
[2] Canc Inst New Jersey, Piscataway, NJ 08901 USA
[3] Human Genet Inst New Jersey, Piscataway, NJ 08854 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Ctr Funct Canc Epigenet, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
[7] Harvard Med Sch, Boston, MA 02115 USA
[8] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
关键词
differentiation; epigenetic control; stem cells; transcription factors; transcriptional regulation; SECRETORY PRECURSORS; DNA METHYLATION; TRANSCRIPTION; CHROMATIN; ENHANCERS; PROTEINS; DISTINCT; DEDIFFERENTIATION; SPECIFICATION; HOMEOSTASIS;
D O I
10.1152/ajpgi.00084.2020
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To fulfill the lifelong need to supply diverse epithelial cells, intestinal stem cells (ISCs) rely on executing accurate transcriptional programs. This review addresses the mechanisms that control those programs. Genes that define cell behaviors and identities are regulated principally through thousands of dispersed enhancers, each individually <1 kb long and positioned from a few to hundreds of kilobases away from transcription start sites, upstream or downstream from coding genes or within introns. Wnt, Notch. and other epithelial control signals feed into these cis-regulatory DNA elements, which are also common loci of polymorphisms and mutations that confer disease risk. Cell-specific gene activity requires promoters to interact with the correct combination of signal-responsive enhancers. We review the current state of knowledge in ISCs regarding active enhancers, the nucleosome modifications that may enable appropriate and hinder inappropriate enhancer-promoter contacts, and the roles of lineage-restricted transcription factors.
引用
收藏
页码:G189 / G196
页数:8
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