A timer for analyzing temporally dynamic changes in transcription during differentiation in vivo

Author:

Bending David1ORCID,Martín Paz Prieto1ORCID,Paduraru Alina1,Ducker Catherine1,Marzaganov Erik1,Laviron Marie1,Kitano Satsuki2,Miyachi Hitoshi2ORCID,Crompton Tessa3ORCID,Ono Masahiro1ORCID

Affiliation:

1. Department of Life Sciences, Faculty of Natural Sciences, Imperial College London, London, England, UK

2. Institute for Viral Research, Kyoto University, Kyoto, Japan

3. University College London Great Ormond Street Institute of Child Health, London, England, UK

Abstract

Understanding the mechanisms of cellular differentiation is challenging because differentiation is initiated by signaling pathways that drive temporally dynamic processes, which are difficult to analyze in vivo. We establish a new tool, Timer of cell kinetics and activity (Tocky; or toki [time in Japanese]). Tocky uses the fluorescent Timer protein, which spontaneously shifts its emission spectrum from blue to red, in combination with computer algorithms to reveal the dynamics of differentiation in vivo. Using a transcriptional target of T cell receptor (TCR) signaling, we establish Nr4a3-Tocky to follow downstream effects of TCR signaling. Nr4a3-Tocky reveals the temporal sequence of events during regulatory T cell (Treg) differentiation and shows that persistent TCR signals occur during Treg generation. Remarkably, antigen-specific T cells at the site of autoimmune inflammation also show persistent TCR signaling. In addition, by generating Foxp3-Tocky, we reveal the in vivo dynamics of demethylation of the Foxp3 gene. Thus, Tocky is a tool for cell biologists to address previously inaccessible questions by directly revealing dynamic processes in vivo.

Funder

Biotechnology and Biological Sciences Research Council

Medical Research Council

Great Ormond Street Hospital Children’s Charity

Publisher

Rockefeller University Press

Subject

Cell Biology

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