[HTML][HTML] Mediator complex dependent regulation of cardiac development and disease
CE Grueter - Genomics, proteomics & bioinformatics, 2013 - Elsevier
CE Grueter
Genomics, proteomics & bioinformatics, 2013•ElsevierCardiovascular disease (CVD) is a leading cause of morbidity and mortality. The risk factors
for CVD include environmental and genetic components. Human mutations in genes
involved in most aspects of cardiovascular function have been identified, many of which are
involved in transcriptional regulation. The Mediator complex serves as a pivotal
transcriptional regulator that functions to integrate diverse cellular signals by multiple
mechanisms including recruiting RNA polymerase II, chromatin modifying proteins and non …
for CVD include environmental and genetic components. Human mutations in genes
involved in most aspects of cardiovascular function have been identified, many of which are
involved in transcriptional regulation. The Mediator complex serves as a pivotal
transcriptional regulator that functions to integrate diverse cellular signals by multiple
mechanisms including recruiting RNA polymerase II, chromatin modifying proteins and non …
Cardiovascular disease (CVD) is a leading cause of morbidity and mortality. The risk factors for CVD include environmental and genetic components. Human mutations in genes involved in most aspects of cardiovascular function have been identified, many of which are involved in transcriptional regulation. The Mediator complex serves as a pivotal transcriptional regulator that functions to integrate diverse cellular signals by multiple mechanisms including recruiting RNA polymerase II, chromatin modifying proteins and non-coding RNAs to promoters in a context dependent manner. This review discusses components of the Mediator complex and the contribution of the Mediator complex to normal and pathological cardiac development and function. Enhanced understanding of the role of this core transcriptional regulatory complex in the heart will help us gain further insights into CVD.
Elsevier