z-logo
Premium
Critical role of the p400/mDomino chromatin‐remodeling ATPase in embryonic hematopoiesis
Author(s) -
Ueda Takeshi,
WatanabeFukunaga Rie,
Ogawa Hironori,
Fukuyama Hidehiro,
Higashi Yujiro,
Nagata Shigekazu,
Fukunaga Rikiro
Publication year - 2007
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1111/j.1365-2443.2007.01080.x
Subject(s) - biology , hox gene , chromatin , yolk sac , microbiology and biotechnology , erythropoiesis , chromatin remodeling , mutant , embryonic stem cell , gene , gene expression , embryo , genetics , medicine , anemia
The SWI2/SNF2 family ATPase, p400/mDomino, is a core subunit of a large chromatin‐remodeling complex, and is currently suggested to play a unique function in histone variant exchange, a process by which chromatin structure is altered. Here, we investigated the role of p400/mDomino in mammalian development by generating mutant mice with a targeted deletion of the N‐terminal domain of p400/mDomino (referred to as mDom ΔN/ΔN ). The mDom ΔN/ΔN mice died on embryonic day 11.5 (E11.5), and displayed an anemic appearance and slight deformity of the neural tube. DNA microarray and quantitative RT‐PCR analyses revealed that all of the embryonic globin genes and a globin chaperone gene were poorly expressed in the mDom ΔN/ΔN embryo and yolk sac on E8.5, indicating that primitive erythropoiesis was impaired. A hematopoietic colony assay indicated that the hematopoietic activity of the yolk sac was significantly blocked in the mutant mice. We also found that the expression of a limited set of Hox genes, including Hoxa7, Hoxa9 and Hoxb9, was drastically enhanced in the mDom ΔN/ΔN yolk sacs. These results suggest that p400/mDomino plays a critical role in embryonic hematopoiesis by regulating the expression of developmentally essential genes such as those in the Hox gene cluster.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here