The C elegans CBFβ homologue BRO-1 interacts with the Runx factor, RNT-1, to promote stem cell proliferation and self-renewal

被引:44
作者
Kagoshima, Hiroshi [1 ]
Nimmo, Rachael
Saad, Nicole
Tanaka, Junko
Miwa, Yoshihiro
Mitani, Shohei
Kohara, Yuji
Woollard, Alison
机构
[1] Natl Inst Genet, Gen Biol Lab, Mishima, Shizuoka 411, Japan
[2] Univ Oxford, Dept Biochem, Genet Unit, Oxford OX1 3QU, England
[3] Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 305, Japan
[4] Precursory Res & Embroyonic Sci & Technol, Okazaki, Aichi 444, Japan
[5] Tokyo Womens Med Univ, Sch Med, Dept Physiol, Tokyo 162, Japan
来源
DEVELOPMENT | 2007年 / 134卷 / 21期
基金
英国医学研究理事会;
关键词
C; elegans; CBF beta; stem cell; proliferation; self-renewal; Runx;
D O I
10.1242/dev.008276
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this report, we investigate the C. elegans CBF beta homologue, BRO- 1. bro- 1 mutants have a similar male- specific sensory ray loss phenotype to rnt- 1 ( the C. elegans homologue of the mammalian CBF beta- interacting Runx factors), caused by failed cell divisions in the seam lineages. Our studies indicate that BRO- 1 and RNT- 1 form a cell proliferation- promoting complex, and that BRO- 1 increases both the affinity and specificity of RNT- 1- DNA interactions. Overexpression of bro- 1, like rnt- 1, leads to an expansion of seam cell number and co- overexpression of bro- 1 and rnt- 1 results in massive seam cell hyperplasia. Finally, we find that BRO- 1 appears to act independently of RNT- 1 in certain situations. These studies provide new insights into the function and regulation of this important cancer- associated DNA- binding complex in stem cells and support the view that Runx/ CBF beta factors have oncogenic potential.
引用
收藏
页码:3905 / 3915
页数:11
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