Signal transduction pathways, intrinsic regulators, and the control of cell fate choice

被引:31
作者
Fossett, Nancy [1 ,2 ]
机构
[1] Univ Maryland, Sch Med, Ctr Vasc & Inflammatory Dis, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Pathol, Baltimore, MD 21201 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2013年 / 1830卷 / 02期
基金
美国国家卫生研究院;
关键词
GATA; Friend of GATA; JAK/STAT; Bone morphogenic protein; Hedgehog; Hematopoiesis; HEMATOPOIETIC STEM-CELLS; ZINC-FINGER PROTEIN; DROSOPHILA-LYMPH GLAND; TRANSCRIPTION FACTOR GATA-2; U-SHAPED FUNCTIONS; LARVAL HEMATOPOIESIS; SELF-RENEWAL; MALIGNANT HEMATOPOIESIS; LINEAGE COMMITMENT; HEMOCYTE LINEAGES;
D O I
10.1016/j.bbagen.2012.06.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Background: Information regarding changes in organismal status is transmitted to the stem cell regulatory machinery by a limited number of signal transduction pathways. Consequently, these pathways derive their functional specificity through interactions with stem cell intrinsic master regulators, notably transcription factors. Identifying the molecular underpinnings of these interactions is critical to understanding stem cell function. Scope of review: This review focuses on studies in Drosophila that identify the gene regulatory basis for interactions between three different signal transduction pathways and an intrinsic master transcriptional regulator in the context of hematopoietic stem-like cell fate choice. Specifically, the interface between the GATA: FOG regulatory complex and the JAK/STAT, BMP, and Hedgehog pathways is examined. Major conclusions: The GATA:FOG complex coordinates information transmitted by at least three different signal transduction pathways as a means to control stem-like cell fate choice. This illustrates emerging principles concerning regulation of stem cell function and describes a gene regulatory link between changes in organismal status and stem cell response. General significance: The Drosophila model system offers a powerful approach to identify the molecular basis of how stem cells receive, interpret, and then respond to changes in organismal status. This article is part of a Special Issue entitled: Biochemistry of Stem Cells. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:2375 / 2384
页数:10
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