Literature DB >> 6453716

Evidence for new forms of cardiac myosin heavy chains in mechanical heart overloading and in ageing.

C Klotz, B Swynghedauw, H Mendes, F Marotte, J J Leger.   

Abstract

Heavy chains of myosin rods and subfragment 1 were isolated from normal hearts and from mechanically overloaded hearts of young and older rats. These myosin heavy-chain fragments were cleaved by cyanogen bromide or partially proteolysed by pronase and by chymotrypsin after denaturation with sodium dodecyl sulfate. The peptides, analyzed by electrophoresis on a one-dimensional polyacrylamide slab gel, varied depending on the origin of the cardiac myosin heavy chains. Some bands present in the peptide patterns of the normal heart of young rats were missing from the pattern of greatly hypertrophied hearts and vice versa. We conclude that mechanical overloading of the heart stimulates the synthesis of cardiac myosin 'isozyme' with a heavy-chain primary structure which is different from that observed in the normal heart of young rat. The patterns from myosin heavy-chain peptides from the hearts of older rats were different from those for peptides from young rat hearts; these results also indicate the presence of a new myosin heavy chain specific to ageing. No difference was detected between the peptide patterns of heavy chains isolated from hypertrophied hearts of young and older rats, and those isolated from normal hearts of older rats.

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Year:  1981        PMID: 6453716     DOI: 10.1111/j.1432-1033.1981.tb05253.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  10 in total

1.  Expression of human beta-myosin heavy chain fragments in Escherichia coli; localization of actin interfaces on cardiac myosin.

Authors:  P Eldin; M Le Cunff; K W Diederich; T Jaenicke; B Cornillon; D Mornet; H P Vosberg; J J Léger
Journal:  J Muscle Res Cell Motil       Date:  1990-10       Impact factor: 2.698

2.  RNA transcription in myocardial-cell nuclei during postnatal development. A study establishing an assay system for transcription in vitro.

Authors:  J D McCully; C C Liew
Journal:  Biochem J       Date:  1988-12-01       Impact factor: 3.857

3.  Mapping of the actomyosin interfaces.

Authors:  P Eldin; M Le Cunff; H P Vosberg; D Mornet; J J Léger
Journal:  Proc Natl Acad Sci U S A       Date:  1994-03-29       Impact factor: 11.205

Review 4.  Contractile proteins in muscle disease.

Authors:  P Cummins
Journal:  J Muscle Res Cell Motil       Date:  1983-02       Impact factor: 2.698

5.  Adult cardiac muscle cells in long-term serum-free culture: myofibrillar organization and expression of myosin heavy chain isoforms.

Authors:  A C Nag; M L Lee; J R Kosiur
Journal:  In Vitro Cell Dev Biol       Date:  1990-05

6.  Expression of myosin isoenzymes in cardiac-muscle cells in culture.

Authors:  A C Nag; M Cheng
Journal:  Biochem J       Date:  1984-07-01       Impact factor: 3.857

7.  Atrial and ventricular myosins from human hearts. II. Isoenzyme distribution after myocardial infarction.

Authors:  U Hoffmann; C Axmann; N Palm
Journal:  Basic Res Cardiol       Date:  1987 Jul-Aug       Impact factor: 17.165

8.  Effects of aging on atrial and ventricular human myosin.

Authors:  S K Banerjee; J Wiener
Journal:  Basic Res Cardiol       Date:  1983 Nov-Dec       Impact factor: 17.165

9.  Transitions in human atrial and ventricular myosin light-chain isoenzymes in response to cardiac-pressure-overload-induced hypertrophy.

Authors:  P Cummins
Journal:  Biochem J       Date:  1982-07-01       Impact factor: 3.857

10.  The cardiac myosin heavy chain Arg-403-->Gln mutation that causes hypertrophic cardiomyopathy does not affect the actin- or ATP-binding capacities of two size-limited recombinant myosin heavy chain fragments.

Authors:  P Eldin; M Le Cunff; D Mornet; J J Leger
Journal:  Biochem J       Date:  1995-03-01       Impact factor: 3.857

  10 in total

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