Distinct from the common impression, the genomes of individual cells in our body are not exactly homogenous or static. Heterogeneity and dynamic changes occur in many cases, such as aging, cancer and HIV infection. Detecting these single cell events in a live animal remains a major challenge. In the proposed project, we plan to validate and further develop our recently invented CRISPR imaging technique in a multicellular organism. This technique utilizes the CRISPR/Cas9 system to fluorescently label specific, endogenous genomic loci for microscopy detection. Here, we will use the nematode C. elegans as the model organism to validate and benchmark CRISPR imaging as a technology to measure the size of repetitive genomic elements such as telomeres as well as the copy number of genes. We will also improve the sensitivity of CRISPR imaging for the detection of non-repetitive genomic elements. Finally, we will apply CRISPR imaging to the study of telomere length change at the single cell level during C. elegans development and aging.
We propose to validate and further develop our recently invented CRISPR imaging technology as a tool to analyze the size, copy number, and other aspects of genomics elements such as telomeres in a live animal. This tool will be instrumental in monitoring genomic events as in aging, cancer and HIV infection, etc.
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| Mcgorty, Ryan; Xie, Dan; Huang, Bo (2017) High-NA open-top selective-plane illumination microscopy for biological imaging. Opt Express 25:17798-17810 |
| Guan, Juan; Liu, Harrison; Shi, Xiaoyu et al. (2017) Tracking Multiple Genomic Elements Using Correlative CRISPR Imaging and Sequential DNA FISH. Biophys J 112:1077-1084 |
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| Chen, Baohui; Guan, Juan; Huang, Bo (2016) Imaging Specific Genomic DNA in Living Cells. Annu Rev Biophys 45:1-23 |
| Kamiyama, Daichi; Sekine, Sayaka; Barsi-Rhyne, Benjamin et al. (2016) Versatile protein tagging in cells with split fluorescent protein. Nat Commun 7:11046 |
