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RUNX1及其直系同源物在决定造血细胞命运中的潜在作用。

Potential roles for RUNX1 and its orthologs in determining hematopoietic cell fate.

作者信息

Tracey W D, Speck N A

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125, USA.

出版信息

Semin Cell Dev Biol. 2000 Oct;11(5):337-42. doi: 10.1006/scdb.2000.0186.

Abstract

Runx1 (also known as AML1, Cbfa2 and Pebpa2b) and Cbfb encode a DNA-binding alpha subunit and the non-DNA-binding beta subunit of a mammalian core-binding factor (CBF). The discovery of RUNX1 and CBFB as genes rearranged in human leukemias prompted predictions that both genes would play important roles in normal hematopoiesis. These predictions were borne out, as indeed Runx1 and its Xenopus and Drosophila homologs, Xaml and lozenge (lz), appear to determine hematopoietic cell fate during development. We will review what is known about Runx1 function in hematopoiesis in three model organisms, mouse, frog and fly, focusing on the earliest events of hematopoietic cell emergence in the embryo.

摘要

Runx1(也称为AML1、Cbfa2和Pebpa2b)和Cbfb分别编码哺乳动物核心结合因子(CBF)的DNA结合α亚基和非DNA结合β亚基。RUNX1和CBFB作为在人类白血病中发生重排的基因被发现,这促使人们预测这两个基因在正常造血过程中都将发挥重要作用。这些预测得到了证实,因为Runx1及其非洲爪蟾和果蝇的同源物Xaml和菱形基因(lz)似乎在发育过程中决定造血细胞的命运。我们将综述在三种模式生物(小鼠、青蛙和果蝇)中已知的Runx1在造血过程中的功能,重点关注胚胎中造血细胞出现的最早事件。

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