Regeneration, repair and remembering identity: the three Rs of Hox gene expression

被引:103
作者
Wang, Kevin C. [1 ,2 ]
Helms, Jill A. [3 ]
Chang, Howard Y. [1 ]
机构
[1] Stanford Univ, Sch Med, Program Epithelial Biol, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94115 USA
[3] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
NONCODING RNAS; HOMEOBOX GENES; NEURAL CREST; PLANARIAN REGENERATION; VERTEBRATE DEVELOPMENT; RESPONSE ELEMENTS; MUSCLE-CELLS; STEM-CELLS; CHROMATIN; PROTEINS;
D O I
10.1016/j.tcb.2009.03.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hox genes encode transcription factors that specify embryonic positional identity in cells and guide tissue differentiation. Recent advances have greatly increased our understanding of the epigenetic mechanisms that ensure the faithful expression of Hox genes in adult cells and which involve the interplay of histone methylation, demethylation and intergenic transcription of long non-coding RNAs. The transcriptional memory of Hox genes poses both an opportunity and a challenge for regenerative medicine. Matching the positional identity of transplanted stem cells with that of the host environment, as reflected by their respective Hox profiles, is likely to be required to achieve regenerative healing. Strategies to manipulate the plasticity of Hox gene expression will probably become a major focus in regenerative medicine.
引用
收藏
页码:268 / 275
页数:8
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