MIR-206 regulates connexin43 expression during skeletal muscle development

C Anderson, H Catoe, R Werner - Nucleic acids research, 2006 - academic.oup.com
C Anderson, H Catoe, R Werner
Nucleic acids research, 2006academic.oup.com
Skeletal myoblast fusion in vitro requires the expression of connexin43 (Cx43) gap junction
channels. However, gap junctions are rapidly downregulated after the initiation of myoblast
fusion in vitro and in vivo. In this study we show that this downregulation is accomplished by
two related microRNAs, miR-206 and miR-1, that inhibit the expression of Cx43 protein
during myoblast differentiation without altering Cx43 mRNA levels. Cx43 mRNA contains
two binding sites for miR-206/miR-1 in its 3′-untranslated region, both of which are …
Abstract
Skeletal myoblast fusion in vitro requires the expression of connexin43 (Cx43) gap junction channels. However, gap junctions are rapidly downregulated after the initiation of myoblast fusion in vitro and in vivo. In this study we show that this downregulation is accomplished by two related microRNAs, miR-206 and miR-1, that inhibit the expression of Cx43 protein during myoblast differentiation without altering Cx43 mRNA levels. Cx43 mRNA contains two binding sites for miR-206/miR-1 in its 3′-untranslated region, both of which are required for efficient downregulation. While it has been demonstrated before that miR-1 is involved in myogenesis, in this work we show that miR-206 is also upregulated during perinatal skeletal muscle development in mice in vivo and that both miR-1 and miR-206 downregulate Cx43 expression during myoblast fusion in vitro. Proper development of singly innervated muscle fibers requires muscle contraction and NMJ terminal selection and it is hypothesized that prolonged electrical coupling via gap junctions may be detrimental to this process. This work details the mechanism by which initial downregulation of Cx43 occurs during myogenesis and highlights the tight control mechanisms that are utilized for the regulation of gap junctions during differentiation and development.
Oxford University Press