The Mi-2-like Smed-CHD4 gene is required for stem cell differentiation in the planarian Schmidtea mediterranea

被引:78
作者
Scimone, M. Lucila [1 ]
Meisel, Joshua [1 ]
Reddien, Peter W. [1 ,2 ]
机构
[1] MIT, Howard Hughes Med Inst, Whitehead Inst, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
来源
DEVELOPMENT | 2010年 / 137卷 / 08期
关键词
CHD4; Differentiation; Planaria; Regeneration; Stem cells; CHROMATIN REMODELER MI-2-BETA; HISTONE DEACETYLASE; DEVELOPMENTAL REGULATORS; EPIGENETIC REGULATION; SELF-RENEWAL; C-ELEGANS; REGENERATION; COMPLEX; COMPONENT; PROTEIN;
D O I
10.1242/dev.042051
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Freshwater planarians are able to regenerate any missing part of their body and have extensive tissue turnover because of the action of dividing cells called neoblasts. Neoblasts provide an excellent system for in vivo study of adult stem cell biology. We identified the Smed-CHD4 gene, which is predicted to encode a chromatin-remodeling protein similar to CHD4/Mi-2 proteins, as required for planarian regeneration and tissue homeostasis. Following inhibition of Smed-CHD4 with RNA interference (RNAi), neoblast numbers were initially normal, despite an inability of the animals to regenerate. However, the proliferative response of neoblasts to amputation or growth stimulation in Smed-CHD4 (RNAi) animals was diminished. Smed-CHD4(RNAi) animals displayed a dramatic reduction in the numbers of certain neoblast progeny cells. Smed-CHD4 was required for the formation of these neoblast progeny cells. Together, these results indicate that Smed-CHD4 is required for neoblasts to produce progeny cells committed to differentiation in order to control tissue turnover and regeneration and suggest a crucial role for CHD4 proteins in stem cell differentiation.
引用
收藏
页码:1231 / 1241
页数:11
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