Heterochromatin Dynamics during the Differentiation Process Revealed by the DNA Methylation Reporter Mouse, MethylRO

Jun Ueda(The University of Osaka), Kazumitsu Maehara(Kyushu University), Daisuke Mashiko(The University of Osaka), Takako Ichinose(Kyushu University), Tatsuma Yao(Fuso Pharmaceutical Industries (Japan)), Mayuko Hori(The University of Osaka), Yuko Sato(The University of Osaka), Hiroshi Kimurâ(The University of Osaka), Yasuyuki Ohkawa(Kyushu University), Kazuo Yamagata(The University of Osaka)
Stem Cell Reports
June 1, 2014
Cited by 55Open Access
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Abstract

In mammals, DNA is methylated at CpG sites, which play pivotal roles in gene silencing and chromatin organization. Furthermore, DNA methylation undergoes dynamic changes during development, differentiation, and in pathological processes. The conventional methods represent snapshots; therefore, the dynamics of this marker within living organisms remains unclear. To track this dynamics, we made a knockin mouse that expresses a red fluorescent protein (RFP)-fused methyl-CpG-binding domain (MBD) protein from the ROSA26 locus ubiquitously; we named it MethylRO (methylation probe in ROSA26 locus). Using this mouse, we performed RFP-mediated methylated DNA immunoprecipitation sequencing (MeDIP-seq), whole-body section analysis, and live-cell imaging. We discovered that mobility and pattern of heterochromatin as well as DNA methylation signal intensity inside the nuclei can be markers for cellular differentiation status. Thus, the MethylRO mouse represents a powerful bioresource and technique for DNA methylation dynamics studies in developmental biology, stem cell biology, as well as in disease states.


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