Literature DB >> 467857

Sub-cellular distribution of the cytoplasmic myosin heavy chain mRNA during myogenesis.

H P Dym, D S Kennedy, S M Heywood.   

Abstract

In the light of earlier work [1] which demonstrated the presence of a large number of myosin heavy chain (MHC) transcripts in chick myoblasts prior to cell fusion and the burst of MHC synthesis it was of great interest to determine the subcellular localization of the still inactive transcripts. It has been determined in differentiating muscle cells in culture. Two populations of cells were examined -- monucleated myoblasts just prior to cell fusion and myotubes where at least 80% of the cells were fused. Utilizing a myosin complementary DNA (cDNA) probe [2] it is observed that just prior to cell fusion, when the "burst" of myosin synthesis has not yet occurred, the vast majority of cytoplasmic myosin mRNA transcripts are found in a stored messenger RNA protein complex with a minimal amount found in the heavy polysome fraction. In differentiated myotube cultures, when myosin synthesis is progressing at a high rate, the reverse is found, i.e, the amount of stored myosin messenger RNA (mRNA) is minimal while the largest amount of myosin mRNA transcripts are localized in the polysome fraction. The number of total cytoplasmic myosin transcripts is found to decrease after cell fusion at a time when myosin synthesis is maximal suggesting that the efficiency of translation of myosin mRNA increases during terminal differentiation.

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Year:  1979        PMID: 467857     DOI: 10.1111/j.1432-0436.1979.tb01000.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  10 in total

1.  Quantitation of muscle-specific mRNAs by using cDNA probes during chicken embryonic muscle development in ovo.

Authors:  C R Saidapet; H N Munro; K Valgeirsdóttir; S Sarkar
Journal:  Proc Natl Acad Sci U S A       Date:  1982-05       Impact factor: 11.205

2.  The problem of automation in animal development: confrontation of the concept of cell sociology with biochemical data.

Authors:  R Chandebois
Journal:  Acta Biotheor       Date:  1981       Impact factor: 1.774

3.  Cytoplasmic utilization of liposome-encapsulated myosin heavy chain messenger ribonucleoprotein particles. During muscle cell differentiation.

Authors:  A S Havaranis; S M Heywood
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

4.  Isoacceptor glycine tRNA species during bovine myocardium development.

Authors:  L Meza; J C Vera; W Mellado; I Concha
Journal:  Experientia       Date:  1981-04-15

5.  Developmental regulation of mRNA in mouse heart.

Authors:  A J Ouellette; D E Croall; J Van Ness; J S Ingwall
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

6.  Effect of creatine on contents of myosin heavy chain and myosin-heavy-chain mRNA in steady-state chicken muscle-cell cultures.

Authors:  R B Young; R M Denome
Journal:  Biochem J       Date:  1984-03-15       Impact factor: 3.857

7.  Turnover of the creatine kinase subunits in chicken myogenic cell cultures and in fibroblasts.

Authors:  M Caravatti; J C Perriard
Journal:  Biochem J       Date:  1981-05-15       Impact factor: 3.857

8.  Posttranscriptional control of embryonic rat skeletal muscle protein synthesis. Control at the level of translation by endogenous RNA.

Authors:  C R Vanderburg; M A Nathanson
Journal:  J Cell Biol       Date:  1988-09       Impact factor: 10.539

9.  Uptake and utilization of mRNA by myogenic cells in culture.

Authors:  B Mroczkowski; H P Dym; E J Siegel; S M Heywood
Journal:  J Cell Biol       Date:  1980-10       Impact factor: 10.539

10.  Encapsulation of "core" eIF3, regulatory components of eIF3 and mRNA into liposomes, and their subsequent uptake into myogenic cells in culture.

Authors:  J O'Loughlin; L Lehr; A Havaranis; S M Heywood
Journal:  J Cell Biol       Date:  1981-07       Impact factor: 10.539

  10 in total

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