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Keywords: Biochemistry.
Issue Date: 1982
Publisher: ProQuest Dissertations & Theses
Citation: Source: Dissertation Abstracts International, Volume: 43-11, Section: B, page: 3574.
Abstract: The molecular mechanisms regulating the induction of myosin heavy chain (MHC) gene expression during muscle cell differentiation were studied using a newly constructed rat embryonic skeletal MHC cDNA recombinant plasmid. During in vitro L(,6)E(,9) cell myogenesis, cytoplasmic MHC mRNA content increases a minimum of 500-fold during the first six days of differentiation. Two independent parameters regulating MHC mRNA accumulation were directly measured: (i) MHC mRNA stability (t(, 1/2) = 55-60 hours) is the same in both myotubes and when first detected in myoblasts. (ii) The rate of MHC gene transcription and MHC mRNA synthesis increases approximately 100-fold during myogenesis but is insufficient to account for the entire MHC mRNA accumulation. An additional independent parameter was found to profoundly affect MHC mRNA accumulation. Withdrawal from the cell cycle, as occurs during terminal myogenic differentiation, increases the final accumulation of stable mRNAs, such as MHC, by increasing mRNA effective stability approximately 4-5 fold. The effective stability is a simple function of the intrinsic stability of the mRNA molecule and the rate of cytoplasmic dilution by mitosis defined by the cell generation time. This cell-cycle mediated effect, combined with the induction of MHC mRNA synthesis, completely accounts for MHC mRNA accumulation. A parallel effect occurs in the total cytoplasmic poly(A)('+) mRNA population. Although the rate of synthesis of each of the two major stability components (t(, 1/2) = 5 and 50 hours, respectively) are equally increased 2-3 fold during myogenesis, the composition of the cytoplasmic mRNA population changes due to the preferential accumulation of stable mRNAs. We conclude that both transcriptional and cell-cycle mediated regulation of MHC gene expression is necessary, but either alone not sufficient, to produce the differentiated muscle cell phenotype.
Appears in Collections:Albert Einstein College of Medicine: Doctoral Dissertations

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