Requirement for serum response factor for skeletal muscle growth and maturation revealed by tissue-specific gene deletion in mice
Author(s) -
Shijie Li,
Michael P. Czubryt,
John McAnally,
Rhonda BasselDuby,
James A. Richardson,
Franziska F. Wiebel,
Alfred Nordheim,
Eric N. Olson
Publication year - 2005
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0409103102
Subject(s) - myocardin , serum response factor , skeletal muscle , biology , transcription factor , microbiology and biotechnology , myosin , myocyte , endocrinology , medicine , gene , genetics
Serum response factor (SRF) controls the transcription of muscle genes by recruiting a variety of partner proteins, including members of the myocardin family of transcriptional coactivators. Mice lacking SRF fail to form mesoderm and die before gastrulation, precluding an analysis of the roles of SRF in muscle tissues. To investigate the functions of SRF in skeletal muscle development, we conditionally deleted the Srf gene in mice by skeletal muscle-specific expression of Cre recombinase. In mice lacking skeletal muscle SRF expression, muscle fibers formed, but failed to undergo hypertrophic growth after birth. Consequently, mutant mice died during the perinatal period from severe skeletal muscle hypoplasia. The myopathic phenotype of these mutant mice resembled that of mice expressing a dominant negative mutant of a myocardin family member in skeletal muscle. These findings reveal an essential role for the partnership of SRF and myocardin-related transcription factors in the control of skeletal muscle growth and maturation in vivo.
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