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J Biol Chem ; 273(24): 14975-81, 1998 Jun 12.
Article in English | MEDLINE | ID: mdl-9614104

ABSTRACT

Muscle activity is known to modulate the muscle fiber phenotype. Changes in muscle activity (normal or experimentally induced) lead to modifications of the expression status of several muscle-specific genes. However, the transcription regulatory elements involved in the adaptative response are mainly unknown. The aldolase A muscle-specific promoter, pM, is expressed in adult fast twitch muscle with a preferential expression in fast glycolytic-2B fibers. Its activity is induced during postnatal muscle maturation, suggesting a role of nerve and/or muscle activity. Indeed, denervation of gastrocnemius in newborn mice prevented the activation of the promoter in this muscle, despite the nerve-independent formation of 2B fibers. Although the nerve was necessary for pM onset during development, denervating the gastrocnemius in adults had only mild effects on pM activity. By contrast, a transgene including the pM proximal regulatory sequences that are sufficient to reproduce the 2B fiber-specific expression of the endogenous promoter was shown to be highly sensitive to both neonatal and adult denervation. Transgenes containing muscle-specific pM proximal promoter elements were used to delineate the regulatory elements involved in this response to innervation and changes in the contractile activity pattern. Nerve- and activity-dependent elements could be localized in the 130-base pair-long proximal promoter region of the human aldolase A gene.


Subject(s)
Fructose-Bisphosphate Aldolase/genetics , Gene Expression Regulation, Developmental/genetics , Muscle, Skeletal/innervation , Promoter Regions, Genetic/genetics , Animals , Crosses, Genetic , Genes, Reporter/genetics , Immunohistochemistry , Mice , Mice, Inbred Strains , Mice, Transgenic , Muscle Contraction/genetics , Muscle Contraction/physiology , Muscle Denervation/adverse effects , Muscle Denervation/methods , Muscle Fibers, Fast-Twitch/physiology , Muscle, Skeletal/enzymology , Phenotype , RNA, Messenger/metabolism , Transgenes/genetics
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