This paper presents multi-modal evidence that ZEB1 is a context dependent transcriptional regulator in cardiomyocytes: ZEB1 overexpression drives hypertrophy/fibrosis and systolic dysfunction, whereas cardiomyocyte-specific ZEB1 deletion produces progressive dilated remodeling, sarcomeric disarray, mitochondrial loss and female-biased mortality; ChIP-seq/RNA-seq integration identifies direct ZEB1 promoter binding to epithelial and mitochondrial genes (e.g., Cdh1, Krt8, Acaa2, Smim20) consistent with these phenotypes
ZEB1 is a canonical EMT transcription factor known to repress epithelial genes (e.g., CDH1/E-cadherin) and to act via co-repressors/co-factors in other tissues; the paper's finding that ZEB1 represses epithelial/ECM programs in cardiomyocytes is mechanistically plausible. The additional observation that ZEB1 binds promoter regions of mitochondrial genes and appears to support mitochondrial gene expression and function suggests a context-specific activator role (or cofactor-mediated activation) in cardiomyocytes, which is novel and biologically credible given tissue-specific cofactor repertoires and previous reports of non-canonical roles for EMT TFs
ZEB1 is a bona fide regulator of cardiomyocyte identity and energetics. The balance of evidence supports that maintaining physiologic ZEB1 is necessary for adult cardiomyocyte mitochondrial and sarcomere integrity. Consider ZEB1 and its downstream mitochondrial program (Acaa2, Smim20) as candidate nodes for mechanistic and therapeutic follow-up; prioritize adult-CM-specific occupancy and rescue experiments and dissect sex-differences before translational extrapolation
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