Literature DB >> 7688301

Primary structure of the human muscle acetylcholine receptor. cDNA cloning of the gamma and epsilon subunits.

D Beeson1, M Brydson, M Betty, S Jeremiah, S Povey, A Vincent, J Newsom-Davis.   

Abstract

cDNA sequences encompassing the full coding region for the human muscle acetylcholine receptor (AChR) epsilon and gamma subunits have been isolated. The deduced amino-acid sequences indicate that the mature epsilon subunit contains 473 amino acids and is preceded by a 20-amino-acid signal peptide. As predicted from genomic clones, the gamma subunit contains 495 amino acids preceded by a 22-amino-acid signal peptide. In common with the human alpha, beta, gamma and delta subunits the epsilon subunit is highly conserved between mammalian species. The epsilon subunit gene is not closely linked to the gamma and delta subunits on chromosome 2 but rather is located with the beta subunit on chromosome 17. Expression of the alpha-, beta-, gamma-, delta- and epsilon-subunit cRNAs in rabbit-reticulocyte lysates followed by analysis on SDS/PAGE show glycosylated proteins with apparent molecular masses of 44-60 kDa.

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Year:  1993        PMID: 7688301     DOI: 10.1111/j.1432-1033.1993.tb18027.x

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


  15 in total

1.  Slow-channel myasthenic syndrome caused by enhanced activation, desensitization, and agonist binding affinity attributable to mutation in the M2 domain of the acetylcholine receptor alpha subunit.

Authors:  M Milone; H L Wang; K Ohno; T Fukudome; J N Pruitt; N Bren; S M Sine; A G Engel
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

2.  A comparison of MyoD1 and fetal acetylcholine receptor expression in childhood tumors and normal tissues: implications for the molecular diagnosis of minimal disease in rhabdomyosarcomas.

Authors:  S Gattenloehner; B Dockhorn-Dworniczak; I Leuschner; A Vincent; H K Müller-Hermelink; A Marx
Journal:  J Mol Diagn       Date:  1999-11       Impact factor: 5.568

3.  Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita.

Authors:  S Brownlow; R Webster; R Croxen; M Brydson; B Neville; J P Lin; A Vincent; J Newsom-Davis; D Beeson
Journal:  J Clin Invest       Date:  2001-07       Impact factor: 14.808

4.  The fetal form of the acetylcholine receptor distinguishes rhabdomyosarcomas from other childhood tumors.

Authors:  S Gattenloehner; A Vincent; I Leuschner; S Tzartos; H K Müller-Hermelink; T Kirchner; A Marx
Journal:  Am J Pathol       Date:  1998-02       Impact factor: 4.307

5.  A pathogenetic role for the thymoma in myasthenia gravis. Autosensitization of IL-4- producing T cell clones recognizing extracellular acetylcholine receptor epitopes presented by minority class II isotypes.

Authors:  N Nagvekar; A M Moody; P Moss; I Roxanis; J Curnow; D Beeson; N Pantic; J Newsom-Davis; A Vincent; N Willcox
Journal:  J Clin Invest       Date:  1998-05-15       Impact factor: 14.808

6.  Functional and non-functional isoforms of the human muscle acetylcholine receptor.

Authors:  C F Newland; D Beeson; A Vincent; J Newsom-Davis
Journal:  J Physiol       Date:  1995-12-15       Impact factor: 5.182

Review 7.  History of Myasthenia Gravis Revisited.

Authors:  Feza Deymeer
Journal:  Noro Psikiyatr Ars       Date:  2020-11-07       Impact factor: 1.339

8.  Regulation of acetylcholine receptor gene expression in human myasthenia gravis muscles. Evidences for a compensatory mechanism triggered by receptor loss.

Authors:  T Guyon; A Wakkach; S Poea; V Mouly; I Klingel-Schmitt; P Levasseur; D Beeson; O Asher; S Tzartos; S Berrih-Aknin
Journal:  J Clin Invest       Date:  1998-07-01       Impact factor: 14.808

9.  Overlapping of MINK and CHRNE gene loci in the course of mammalian evolution.

Authors:  Ippeita Dan; Norinobu M Watanabe; Eriko Kajikawa; Takafumi Ishida; Akhilesh Pandey; Akihiro Kusumi
Journal:  Nucleic Acids Res       Date:  2002-07-01       Impact factor: 16.971

10.  Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.

Authors:  C J Hatton; C Shelley; M Brydson; D Beeson; D Colquhoun
Journal:  J Physiol       Date:  2003-01-24       Impact factor: 5.182

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