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Transgenic over-expression of YY1 induces pathologic cardiac hypertrophy in a sex-specific manner.


ABSTRACT: YY1 can activate or repress transcription of various genes. In cardiac myocytes in culture YY1 has been shown to regulate expression of several genes involved in myocyte pathology. YY1 can also acutely protect the heart against detrimental changes in gene expression. In this study we show that cardiac over-expression of YY1 induces pathologic cardiac hypertrophy in male mice, measured by changes in gene expression and lower ejection fraction/fractional shortening. In contrast, female animals are protected against pathologic gene expression changes and cardiac dysfunction. Furthermore, we show that YY1 regulates, in a sex-specific manner, the expression of mammalian enable (Mena), a factor that regulates cytoskeletal actin dynamics and whose expression is increased in several models of cardiac pathology, and that Mena expression in humans with heart failure is sex-dependent. Finally, we show that sex differences in YY1 expression are also observed in human heart failure. In summary, this is the first work to show that YY1 has a sex-specific effect in the regulation of cardiac pathology.

SUBMITTER: Stauffer BL 

PROVIDER: S-EPMC4449792 | biostudies-other | 2015 Jun

REPOSITORIES: biostudies-other

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Transgenic over-expression of YY1 induces pathologic cardiac hypertrophy in a sex-specific manner.

Stauffer Brian L BL   Dockstader Karen K   Russell Gloria G   Hijmans Jamie J   Walker Lisa L   Cecil Mackenzie M   Demos-Davies Kimberly K   Medway Allen A   McKinsey Timothy A TA   Sucharov Carmen C CC  

Biochemical and biophysical research communications 20150429 2


YY1 can activate or repress transcription of various genes. In cardiac myocytes in culture YY1 has been shown to regulate expression of several genes involved in myocyte pathology. YY1 can also acutely protect the heart against detrimental changes in gene expression. In this study we show that cardiac over-expression of YY1 induces pathologic cardiac hypertrophy in male mice, measured by changes in gene expression and lower ejection fraction/fractional shortening. In contrast, female animals are  ...[more]

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