학술논문

Preliminary development of an assay for detection of TERT expression, telomere length, and telomere elongation in single cells
Document Type
article
Source
PLOS ONE. 13(12)
Subject
Biochemistry and Cell Biology
Biological Sciences
Genetics
Cancer
Aging
1.1 Normal biological development and functioning
Underpinning research
Gene Expression Regulation
Enzymologic
HeLa Cells
Humans
Telomerase
Telomere
Telomere Homeostasis
Hela Cells
General Science & Technology
Language
Abstract
The telomerase enzyme enables unlimited proliferation of most human cancer cells by elongating telomeres and preventing replicative senescence. Despite the critical importance of telomerase in cancer biology, challenges detecting telomerase activity and expression in individual cells have hindered the ability to study patterns of telomerase expression and function across heterogeneous cell populations. While sensitive assays to ascertain telomerase expression and function exist, these approaches have proven difficult to implement at the single cell level. Here, we validate in situ RNAscope detection of the telomerase TERT mRNA and couple this assay with our recently described TSQ1 method for in situ detection of telomere elongation. This approach enables detection of TERT expression, telomere length, and telomere elongation within individual cells of the population. Using this assay, we show that the heterogeneous telomere elongation observed across a HeLa cell population is in part driven by variable expression of the TERT gene. Furthermore, we show that the absence of detectable telomere elongation in some TERT-positive cells is the result of inhibition by the telomeric shelterin complex. This combined assay provides a new approach for understanding the integrated expression, function, and regulation of telomerase at the single cell level.