The Zebrafish moonshine gene encodes transcriptional intermediary factor 1γ, an essential regulator of hematopoiesis

被引:108
作者
Ransom, DG
Bahary, N
Niss, K
Traver, D
Burns, C
Trede, NS
Paffett-Lugassy, N
Saganic, WJ
Lim, CA
Hersey, C
Zhou, Y
Barut, BA
Lin, S
Kingsley, PD
Palis, J
Orkin, SH
Zon, LI [1 ]
机构
[1] Howard Hughes Med Inst, Chevy Chase, MD USA
[2] Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA USA
[5] Univ Rochester, Med Ctr, Dept Pediat, Rochester, NY 14642 USA
[6] Univ Rochester, Med Ctr, Ctr Human Genet & Mol Pediat Dis, Rochester, NY 14642 USA
关键词
D O I
10.1371/journal.pbio.0020237
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hematopoiesis is precisely orchestrated by lineage-specific DNA-binding proteins that regulate transcription in concert with coactivators and corepressors. Mutations in the zebrafish moonshine (mon) gene specifically disrupt both embryonic and adult hematopoiesis, resulting in severe red blood cell aplasia. We report that mon encodes the zebrafish ortholog of mammalian transcriptional intermediary factor 1gamma (TIF1gamma) (or TRIM33), a member of the TIF1 family of coactivators and corepressors. During development, hematopoietic progenitor cells in mon mutants fail to express normal levels of hematopoietic transcription factors, including gata1, and undergo apoptosis. Three different mon mutant alleles each encode premature stop codons, and enforced expression of wild-type tif1gamma mRNA rescues embryonic hematopoiesis in homozygous man mutants. Surprisingly, a high level of zygotic tif1gamma mRNA expression delineates ventral mesoderm during hematopoietic stem cell and progenitor formation prior to gata1 expression. Transplantation studies reveal that tif1gamma functions in a cell-autonomous manner during the differentiation of erythroid precursors. Studies in murine erythroid cell lines demonstrate that Tif1gamma protein is localized within novel nuclear foci, and expression decreases during erythroid cell maturation. Our results establish a major role for this transcriptional intermediary factor in the differentiation of hematopoietic cells in vertebrates.
引用
收藏
页码:1188 / 1196
页数:9
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