A system to analyze the initiation of random X-chromosome inactivation using time-lapse imaging of single cells

In female eutherian mammal development, X-chromosome inactivation (XCI) of one of the two X chromosomes is initiated early. Understanding the relationship between the initiation of XCI and cell fate is critical for understanding early female development and requires a system that can monitor XCI in single living cells. Traditional embryonic stem cells (ESCs) used for XCI studies often lose X chromosomes spontaneously during culture and differentiation, making accurate monitoring difficult. Additionally, most XCI assessment methods necessitate cell disruption, hindering cell fate tracking. We developed the Momiji (version 2) ESC line to address these difficulties, enabling real-time monitoring of X-chromosome activity via fluorescence. We inserted green and red fluorescent reporter genes and neomycin and puromycin resistance genes into the two X chromosomes of PGK12.1 ESCs, creating a female ESC line that retains two X chromosomes more faithfully during differentiation. Momiji (version 2) ESCs exhibit a more stable XX karyotype than other ESC lines, including the parental PGK12.1 line. This new tool offers valuable insights into the relationship between XCI and cell fate, improving our understanding of early female development.

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Publication Details

Journal
Scientific Reports
Published
2024-09-02
DOI
https://doi.org/10.1038/s41598-024-71105-y
Citations
2
Primary Topic
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Type
article
Field-Weighted Citation Impact
1.10

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article

A system to analyze the initiation of random X-chromosome inactivation using time-lapse imaging of single cells

Shin Kobayashi, Yu Hatano, Hikaru Suenaga, Manami Koshiguchi et al.
2 citations
Scientific Reports
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
1.10
article

A system to analyze the initiation of random X-chromosome inactivation using time-lapse imaging of single cells

Shin Kobayashi, Yu Hatano, Hikaru Suenaga, Manami Koshiguchi, Nao Yonezawa, Kazuo Yamagata
article en
2 citations

Abstract

In female eutherian mammal development, X-chromosome inactivation (XCI) of one of the two X chromosomes is initiated early. Understanding the relationship between the initiation of XCI and cell fate is critical for understanding early female development and requires a system that can monitor XCI in single living cells. Traditional embryonic stem cells (ESCs) used for XCI studies often lose X chromosomes spontaneously during culture and differentiation, making accurate monitoring difficult. Additionally, most XCI assessment methods necessitate cell disruption, hindering cell fate tracking. We developed the Momiji (version 2) ESC line to address these difficulties, enabling real-time monitoring of X-chromosome activity via fluorescence. We inserted green and red fluorescent reporter genes and neomycin and puromycin resistance genes into the two X chromosomes of PGK12.1 ESCs, creating a female ESC line that retains two X chromosomes more faithfully during differentiation. Momiji (version 2) ESCs exhibit a more stable XX karyotype than other ESC lines, including the parental PGK12.1 line. This new tool offers valuable insights into the relationship between XCI and cell fate, improving our understanding of early female development.

Scientific ReportsVol. 14(1)
RIKEN Center for Biosystems Dynamics Research (JP), University of Yamanashi (JP), National Institute of Advanced Industrial Science and Technology (JP), Kindai University (JP)
Takeda Science Foundation, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
Gender equality
Openalex Percentile: Top 19%
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
1.10
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