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Updated: May 7, 2026

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Single Cell Transcriptional Profiling of Adult Mouse Cardiomyocytes
Published on: December 28, 2011
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The Core Circadian Clock Factor, Bmal1, Transduces Sex-specific Differences in Both Rhythmic and Nonrhythmic Gene
Xiping Zhang1, Spencer B Procopio1, Haocheng Ding2
1Department of Physiology and Aging, University of Florida, Gainesville, FL 32610, USA.
Function (Oxford, England)
|December 10, 2024
Summary
Male and female mouse hearts show distinct circadian gene expression patterns. Cardiomyocyte-specific Bmal1 loss significantly reduces these sex differences, highlighting its role in cardiac sex-specific gene regulation.
Area of Science:
- Cardiovascular Biology
- Chronobiology
- Molecular Genetics
Background:
- Cardiovascular diseases (CVDs) show sex-based disparities.
- Disrupted circadian rhythms are linked to CVD development.
- Sex differences in the cardiac circadian clock remain poorly understood.
Purpose of the Study:
- Investigate sex-specific differences in the mouse cardiac circadian transcriptome.
- Determine the role of the core circadian clock factor Bmal1 in sex-specific cardiac gene expression.
Main Methods:
- Comparative analysis of cardiac circadian transcriptomes in male and female mice.
- Conditional knockout of Bmal1 in adult cardiomyocytes.
- RNA sequencing to assess gene expression changes.
Main Results:
- Cardiac circadian transcriptomes are highly sex-specific, with more rhythmically expressed genes (REGs) in females.
- Loss of cardiomyocyte Bmal1 diminished sex differences in REGs and overall gene expression between sexes.
- Sex-specific regulation of cardiac transcription factors (Gata4, Nkx2-5, Tbx5) was observed.
Conclusions:
- Cardiomyocyte-specific Bmal1 is crucial for sex-specific gene expression in the adult mouse heart.
- The circadian clock plays a significant role in mediating sex differences in cardiac biology.
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