Key result
Review outlines how specific promoters and transcription factors regulate voltage-gated Ca2+ channel gene transcription.
This review highlights the emerging understanding of transcriptional regulation of voltage-gated calcium channels, emphasizing the need for deeper knowledge of their 5' upstream regions to detect alterations causing human disease.
Promoter mapping of Ca2+ channels remains insufficient for clinical variant interpretation; leaves open targeted studies of disease-causing transcriptional alterations.
The transcriptional regulation of voltage‐gated Ca 2+ (Ca V ) channels is an emerging research area that promises to improve our understanding of how many relevant physiological events are shaped in the central nervous system, the skeletal muscle and other tissues. Interestingly, a picture of how transcription of Ca V channel subunit genes is controlled is evolving with the identification of the promoter regions required for tissue‐specific expression and the identification of transcription factors that control their expression. These promoters share several characteristics that include multiple transcriptional start sites, lack of a TATA box and the presence of elements conferring tissue‐selective expression. Likewise, changes in Ca V channel expression occur throughout development, following ischaemia, seizures or chronic drug administration. This review focuses on insights achieved regarding the control of Ca V channel gene expression. To further understand the complexities of expression and to increase the possibilities of detecting Ca V channel alterations causing human disease, a deeper knowledge on the structure of the 5′ upstream regions of the genes encoding these remarkable proteins will be necessary.
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González‐Ramírez et al. (2017) conducted a review in Voltage-gated Ca2+ channel regulation. This review highlights the evolving understanding of how transcription of voltage-gated Ca2+ channel subunit genes is controlled by specific promoter regions and transcription factors.
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