Chromosome therapy Correction of large chromosomal aberrations by inducing ring chromosomes in induced pluripotent stem cells (iPSCs)

被引:13
|
作者
Kim, Taehyun [1 ]
Bershteyn, Marina [2 ]
Wynshaw-Boris, Anthony [1 ,3 ,4 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Genet & Genome Sci, Cleveland, OH 44106 USA
[2] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
关键词
ring chromosomes; induced pluripotent stem cells (iPSCs); Miller Dieker Syndrome (MDS); compensatory uniparental disomy (UPD); chromosome therapy; MILLER-DIEKER-SYNDROME; UNIPARENTAL DISOMY; 17P13.3;
D O I
10.4161/nucl.36300
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fusion of the short (p) and long (q) arms of a chromosome is referred to as a "ring chromosome." Ring chromosome disorders occur in approximately 1 in 50 000-100 000 patients. Ring chromosomes can result in birth defects, mental disabilities, and growth retardation if additional genes are deleted during the formation of the ring. Due to the severity of these large-scale aberrations affecting multiple contiguous genes, no possible therapeutic strategies for ring chromosome disorders have so far been proposed. Our recent study (Bershteyn et al.) using patient-derived fibroblast lines containing ring chromosomes, found that cellular reprogramming of these fibroblasts into induced pluripotent stem cells (iPSCs) resulted in the cell-autonomous correction of the ring chromosomal aberration via compensatory uniparental disomy (UPD). These observations have important implications for studying the mechanism of chromosomal number control and may lead to the development of effective therapies for other, more common, chromosomal aberrations.
引用
收藏
页码:391 / 395
页数:5
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