| Literature DB >> 16867900 |
Hideo Harigae1, Yoko Okitsu, Hisayuki Yokoyama, Tohru Fujiwara, Mitsue Inomata, Shinichiro Takahashi, Naoko Minegishi, Mitsuo Kaku, Takeshi Sasaki.
Abstract
GATA transcription factors have been shown to play important roles in hematopoiesis. GATA-2 is expressed in stem and progenitor cells, and has been speculated to control the proliferation and maintain the immaturity of these cells. To examine whether the function of GATA-2 is changeable according to the differentiation stage, we established GATA-2 overexpressing subclones of K562, which is a leukemic cell line committed to the erythroid lineage. Via an increase in the GATA-2 expression level, the expression levels of erythroid-specific genes including alpha-, beta-, and gamma-globin were increased compared to control cells, while the expression level of GATA-1 was unchanged. Expression of the transferrin receptor was also increased in GATA-2 overexpressing K562 cells when examined by flow cytometry. In addition, the heme content of GATA-2 overexpressing K562 cells was more than 2 times higher than control cells. Chromatin immunoprecipitation analysis showed that GATA-2 protein binding to the GATA element in alpha-globin LCR was increased in GATA-2 overexpressing K562 cells. These findings suggest that GATA-2 could induce erythroid-specific genes without competition with GATA-1 when expressed in erythroid-committed cells, and thus further suggest that temporal and spatial regulation may be important for displaying specific functions of GATA-2.Entities:
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Year: 2006 PMID: 16867900 DOI: 10.1532/IJH97.06020
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490