Program in Cell and Developmental Dynamics, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605.
Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21048-53. doi: 10.1073/pnas.1319097110. Epub 2013 Dec 9.
We describe a transcription activator-like effector (TALE)-based strategy, termed "TALEColor," for labeling specific repetitive DNA sequences in human chromosomes. We designed TALEs for the human telomeric repeat and fused them with any of numerous fluorescent proteins (FPs). Expression of these TALE-telomere-FP fusion proteins in human osteosarcoma's (U2OS) cells resulted in bright signals coincident with telomeres. We also designed TALEs for centromeric sequences unique to certain chromosomes, enabling us to localize specific human chromosomes in live cells. Meanwhile we generated TALE-FPs in vitro and used them as probes to detect telomeres in fixed cells. Using human cells with different average telomere lengths, we found that the TALEColor signals correlated positively with telomere length. In addition, suspension cells were followed by imaging flow cytometry to resolve cell populations with differing telomere lengths. These methods may have significant potential both for basic chromosome and genome research as well as in clinical applications.
我们描述了一种基于转录激活因子样效应物(TALE)的策略,称为“TALEColor”,用于标记人类染色体上特定的重复 DNA 序列。我们设计了针对人类端粒重复序列的 TALEs,并将其与众多荧光蛋白(FPs)中的任何一种融合。这些 TALE-端粒-FP 融合蛋白在人骨肉瘤(U2OS)细胞中的表达导致与端粒一致的明亮信号。我们还设计了针对某些染色体特有的着丝粒序列的 TALEs,使我们能够在活细胞中定位特定的人类染色体。同时,我们在体外生成了 TALE-FPs,并将其用作探针来检测固定细胞中的端粒。使用具有不同平均端粒长度的人类细胞,我们发现 TALEColor 信号与端粒长度呈正相关。此外,通过成像流式细胞术对悬浮细胞进行跟踪,以解析具有不同端粒长度的细胞群体。这些方法在基础染色体和基因组研究以及临床应用中都具有重要的潜在应用价值。