Literature DB >> 3546335

Slow myosin in developing rat skeletal muscle.

M Narusawa, R B Fitzsimons, S Izumo, B Nadal-Ginard, N A Rubinstein, A M Kelly.   

Abstract

Through S1 nuclease mapping using a specific cDNA probe, we demonstrate that the slow myosin heavy-chain (MHC) gene, characteristic of adult soleus, is expressed in bulk hind limb muscle obtained from the 18-d rat fetus. We support these results by use of a monoclonal antibody (mAb) which is highly specific to the adult slow MHC. Immunoblots of MHC peptide maps show the same peptides, uniquely recognized by this antibody in adult soleus, are also identified in 18-d fetal limb muscle. Thus synthesis of slow myosin is an early event in skeletal myogenesis and is expressed concurrently with embryonic myosin. By immunofluorescence we demonstrate that in the 16-d fetus all primary myotubes in future fast and future slow muscles homogeneously express slow as well as embryonic myosin. Fiber heterogeneity arises owing to a developmentally regulated inhibition of slow MHC accumulation as muscles are progressively assembled from successive orders of cells. Assembly involves addition of new, superficial areas of the anterior tibial muscle (AT) and extensor digitorum longus muscle (EDL) in which primary cells initially stain weakly or are unstained with the slow mAb. In the developing AT and EDL, expression of slow myosin is unstable and is progressively restricted as these muscles specialize more and more towards the fast phenotype. Slow fibers persisting in deep portions of the adult EDL and AT are interpreted as vestiges of the original muscle primordium. A comparable inhibition of slow MHC accumulation occurs in the developing soleus but involves secondary, not primary, cells. Our results show that the fate of secondary cells is flexible and is spatially determined. By RIA we show that the relative proportions of slow MHC are fivefold greater in the soleus than in the EDL or AT at birth. After neonatal denervation, concentrations of slow MHC in the soleus rapidly decline, and we hypothesize that, in this muscle, the nerve protects and amplifies initial programs of slow MHC synthesis. Conversely, the content of slow MHC rises in the neonatally denervated EDL. This suggests that as the nerve amplifies fast MHC accumulation in the developing EDL, accumulation of slow MHC is inhibited in an antithetic fashion. Studies with phenylthiouracil-induced hypothyroidism indicate that inhibition of slow MHC accumulation in the EDL and AT is not initially under thyroid regulation. At later stages, the development of thyroid function plays a role in inhibiting slow MHC accumulation in the differentiating EDL and AT.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3546335      PMCID: PMC2114541          DOI: 10.1083/jcb.104.3.447

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  41 in total

1.  DYNAMIC PROPERTIES OF FAST AND SLOW SKELETAL MUSCLES OF THE RAT DURING DEVELOPMENT.

Authors:  R CLOSE
Journal:  J Physiol       Date:  1964-09       Impact factor: 5.182

2.  Myogenic and neurogenic contributions to the development of fast and slow twitch muscles in rat.

Authors:  N A Rubinstein; A M Kelly
Journal:  Dev Biol       Date:  1978-02       Impact factor: 3.582

3.  Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids.

Authors:  A J Berk; P A Sharp
Journal:  Cell       Date:  1977-11       Impact factor: 41.582

4.  Contractile protein isozymes in muscle development: identification of an embryonic form of myosin heavy chain.

Authors:  R G Whalen; K Schwartz; P Bouveret; S M Sell; F Gros
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

5.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

6.  Why are fetal muscles slow?

Authors:  A M Kelly; N A Rubinstein
Journal:  Nature       Date:  1980-11-20       Impact factor: 49.962

7.  Identification of recombinant phages containing sequences from different rat myosin heavy chain genes.

Authors:  U Nudel; D Katcoff; Y Carmon; D Zevin-Sonkin; Z Levi; Y Shaul; M Shani; D Yaffe
Journal:  Nucleic Acids Res       Date:  1980-05-24       Impact factor: 16.971

8.  Rapidly labeled HeLa cell nuclear RNA. II. Base composition and cellular localization of a heterogeneous RNA fraction.

Authors:  R Soeiro; H C Birnboim; J E Darnell
Journal:  J Mol Biol       Date:  1966-08       Impact factor: 5.469

9.  Adaptive transformation of rat soleus motor units during growth.

Authors:  E Kugelberg
Journal:  J Neurol Sci       Date:  1976-03       Impact factor: 3.181

10.  Development of muscle fiber specialization in the rat hindlimb.

Authors:  N A Rubinstein; A M Kelly
Journal:  J Cell Biol       Date:  1981-07       Impact factor: 10.539

View more
  66 in total

1.  Quantification of fibre type regionalisation: an analysis of lower hindlimb muscles in the rat.

Authors:  L C Wang; D Kernell
Journal:  J Anat       Date:  2001-03       Impact factor: 2.610

2.  Proximo-distal organization and fibre type regionalization in rat hindlimb muscles.

Authors:  L C Wang; D Kernell
Journal:  J Muscle Res Cell Motil       Date:  2000       Impact factor: 2.698

3.  Regulation of myosin heavy chain expression during rat skeletal muscle development in vitro.

Authors:  C E Torgan; M P Daniels
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

4.  Active zone density is conserved during synaptic growth but impaired in aged mice.

Authors:  Jie Chen; Takafumi Mizushige; Hiroshi Nishimune
Journal:  J Comp Neurol       Date:  2012-02-01       Impact factor: 3.215

5.  Neural regulation of differentiation of rat skeletal muscle cell types.

Authors:  G K Dhoot
Journal:  Histochemistry       Date:  1992-07

6.  NADH-O2 oxidoreductase activity and mRNA expression of complex I (51 kDa, ND1) in postnatal intrinsic muscle of rat tongue.

Authors:  Toshiya Fujita; Iwao Sato
Journal:  J Anat       Date:  2003-02       Impact factor: 2.610

7.  Aggregation of myonuclei and the spread of slow-tonic myosin immunoreactivity in developing muscle spindles.

Authors:  J Kucera; J M Walro
Journal:  Histochemistry       Date:  1991

8.  Comparison of the foetal development of fibre types in four bovine muscles.

Authors:  B Picard; J Robelin; F Pons; Y Geay
Journal:  J Muscle Res Cell Motil       Date:  1994-08       Impact factor: 2.698

9.  Different metabolic responses to exercise training programmes in single rat muscle fibres.

Authors:  H Takekura; T Yoshioka
Journal:  J Muscle Res Cell Motil       Date:  1990-04       Impact factor: 2.698

10.  Spatial and temporal patterns of myosin heavy chain expression in developing rat extraocular muscle.

Authors:  J K Brueckner; O Itkis; J D Porter
Journal:  J Muscle Res Cell Motil       Date:  1996-06       Impact factor: 2.698

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.