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Publication : Creatine kinase transcript accumulation: effect of nerve during muscle development.

First Author  Washabaugh CH Year  1999
Journal  Dev Dyn Volume  215
Issue  4 Pages  285-96
PubMed ID  10417818 Mgi Jnum  J:56670
Mgi Id  MGI:1342164 Doi  10.1002/(SICI)1097-0177(199908)215:4<285::AID-AJA1>3.0.CO;2-S
Citation  Washabaugh CH, et al. (1999) Creatine kinase transcript accumulation: effect of nerve during muscle development. Dev Dyn 215(4):285-96
abstractText  To determine the role of the nerve in regulating the accumulation of cytoplasmic creatine kinase (CK) mRNAs in hindleg muscles of the developing mouse, the lumbosacral spinal cords of 14-day gestation mice (E14) were laser ablated, and the accumulation of muscle CK (MCK) and brain CK (BCK) mRNAs was evaluated just prior to birth with in situ hybridization. Numbers of molecules of each of these transcripts/ng total RNA in the soleus and extensor digitorum longus (EDL) muscles were determined with competitive PCR and compared to transcripts found in innervated crural muscles. Data suggest that: 1) the level of BCK mRNA accumulation in innervated hindlimb muscles peaks at E16.5 and remains at fetal levels until the second month postnatal, when it falls to the level found in the adult. Given that MCK transcripts meet or exceed adult levels by day 28 postnatal, the 'down-regulation' of the BCK gene and the 'up-regulation' of the MCK gene are not tightly coupled; 2) the developmental switch from BCK to MCK, as the dominant cytoplasmic CK mRNA, occurs in innervated and aneural leg muscles between E14 and E16.5, indicating this switch is not nerve dependent; 3) the absence of innervation has no effect on BCK mRNA accumulation. MCK transcripts/ng total RNA continue to increase in aneural muscle throughout the late fetal period, but from E16.5-E19.5 the MCK transcript levels in aneural muscles become progressively lower than in age-matched innervated muscles. Thus, the accumulation of the muscle specific cytoplasmic CK, but not BCK, transcripts is affected by the absence of innervation during the fetal period. Dev Dyn 1999;215:285-296. Copyright 1999 Wiley-Liss, Inc.
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