Yamamoto M, Takahashi S, Onodera K, Muraosa Y, Engel J D
Centre for Tsukuba Advanced Research Alliance, Institute of Basic Medical Sciences, University of Tsukuba, Japan.
Genes Cells. 1997 Feb;2(2):107-15. doi: 10.1046/j.1365-2443.1997.1080305.x.
All mature blood lineages in the peripheral circulation are derived from pluripotent haematopoietic stem cell. Progressive lineage-restriction of this stem cell is executed, in part, by the interplay and cross-talk between a host of lineage-restricted as well as ubiquitous transcription factors. To elucidate the regulatory mechanisms underlying the erythroid gene regulation, it is essential to understand how individual transcription factors contribute to the regulation of specific target genes, and how these erythroid transcription factor genes are regulated in turn. These key issues of mammalian development have been addressed by examining the activities controlling the prototype transcription factor, GATA-1. The transcriptional regulation of GATA-1 has been intensively investigated, thereby leading to the identification of its developmental stage-specific regulatory sequences. Loss-of-function mutant animals, combined with specific marking of the primitive and definitive erythroid lineages have also shed new insight into how GATA-1 activity is required in vivo at specific developmental stages. Procedures have also been developed for ascertaining whether or not the GATA-1 protein actually binds in vivo to regulatory GATA motifs in candidate target genes. Application of a similar multifaceted approach should enable investigators to examine the physiological roles that any transcription factor might play in vivo during the differentiation of any well defined cell lineage.
外周循环中的所有成熟血细胞谱系均源自多能造血干细胞。该干细胞逐步的谱系限制部分是由众多谱系限制以及普遍存在的转录因子之间的相互作用和相互影响来执行的。为了阐明红细胞生成基因调控的潜在机制,了解单个转录因子如何对特定靶基因的调控发挥作用,以及这些红细胞转录因子基因又是如何反过来被调控的至关重要。通过研究控制原型转录因子GATA-1的活性,已经解决了哺乳动物发育中的这些关键问题。对GATA-1的转录调控进行了深入研究,从而确定了其发育阶段特异性调控序列。功能丧失突变动物,结合原始和定型红细胞谱系的特异性标记,也为GATA-1活性在特定发育阶段体内所需情况提供了新的见解。还开发了用于确定GATA-1蛋白在体内是否实际结合候选靶基因中的调控GATA基序的方法。应用类似的多方面方法应能使研究人员研究任何转录因子在任何明确界定的细胞谱系分化过程中在体内可能发挥的生理作用。