Tracking expression and subcellular localization of RNA and protein species using high-throughput single cell imaging flow cytometry

被引:21
作者
Borah, Sumit [1 ]
Nichols, Lisa A. [2 ,3 ]
Hassman, Lynn M. [2 ,3 ]
Kedes, Dean H. [2 ,3 ,4 ]
Steitz, Joan A. [1 ]
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, Howard Hughes Med Inst, New Haven, CT 06536 USA
[2] Univ Virginia, Myles H Thaler Ctr AIDS & Human Retrovirus Res, Charlottesville, VA 22908 USA
[3] Univ Virginia, Dept Microbiol Immunol & Canc Biol, Charlottesville, VA 22908 USA
[4] Univ Virginia, Dept Med, Charlottesville, VA 22908 USA
关键词
FACS; high-throughput; MIFC; RNA; noncoding; SARCOMA-ASSOCIATED HERPESVIRUS; PRIMARY EFFUSION LYMPHOMA; LATENTLY INFECTED-CELLS; IN-SITU HYBRIDIZATION; KAPOSIS-SARCOMA; GENE-EXPRESSION; MESSENGER-RNA; NUCLEAR IMPORT; KSHV INFECTION; IDENTIFICATION;
D O I
10.1261/rna.033126.112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report a high-throughput application of multispectral imaging flow cytometry (MIFC) for analyzing the expression and localization of both RNA and protein molecules in a heterogeneous population of cells. The approach was developed using polyadenylated nuclear (PAN) RNA, an abundant, noncoding RNA expressed by Kaposi's sarcoma-associated herpesvirus (KSHV) during the lytic phase of infection. High levels of PAN RNA are, in part, dependent on its interaction with poly(A)binding protein C1 (PABPC1), which relocalizes from the cytoplasm to the nucleus of lytically infected cells. We quantitatively tracked the cytoplasmic to nuclear translocation of PABPC1 and examined how this translocation relates to the expression and localization of viral RNA and protein molecules in KSHV-infected cells. This high-throughput approach will be useful for other systems in which changes in subcellular localization of RNA and protein molecules need to be monitored simultaneously.
引用
收藏
页码:1573 / 1579
页数:7
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