Literature DB >> 22941678

Expression of multiple nebulin isoforms in human skeletal muscle and brain.

Jenni Laitila1, Mubashir Hanif, Anders Paetau, Sari Hujanen, Joni Keto, Panu Somervuo, Sanna Huovinen, Bjarne Udd, Carina Wallgren-Pettersson, Petri Auvinen, Peter Hackman, Katarina Pelin.   

Abstract

INTRODUCTION: Nebulin is a large actin-binding protein of the skeletal muscle sarcomere. Multiple isoforms of nebulin are produced from the 183-exon-containing nebulin gene (NEB). Mutations in NEB cause nemaline myopathy, distal myopathy, and core-rod myopathy.
METHODS: Nebulin mRNA expression was assessed by microarrays and RT-PCR in 21 human leg muscle and 2 brain samples. Protein expression was assessed by immunohistochemistry in 5 regions of 1 brain sample.
RESULTS: Nebulin isoform diversity is as high in brain as in skeletal muscle. Isoforms with more than 22 super repeats seem to be more common than previously anticipated. Immunohistochemistry showed nebulin expression predominantly in the cytoplasm of pyramidal neurons but also in the cytoplasm of mainly subcortical endothelial cells.
CONCLUSIONS: Nebulin, as in skeletal muscle, may have a role as an actin filament stabilizer or length regulator in neurons of the human brain, although patients with NEB mutations usually have normal cognition.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22941678     DOI: 10.1002/mus.23380

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  12 in total

1.  A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness.

Authors:  Katarina Pelin; Kirsi Kiiski; Vilma-Lotta Lehtokari; Carina Wallgren-Pettersson
Journal:  J Hum Genet       Date:  2015-01-15       Impact factor: 3.172

2.  Identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness.

Authors:  Hyun-Seok Jin; Jong-Bin Lee; Kyung Kim; Ki-Young Lee; Vit-Na Choi; Jong-Soo Kim; Seon-Yong Jeong; Shin-Young Yim
Journal:  J Hum Genet       Date:  2014-10-09       Impact factor: 3.172

3.  A recurrent copy number variation of the NEB triplicate region: only revealed by the targeted nemaline myopathy CGH array.

Authors:  Kirsi Kiiski; Vilma-Lotta Lehtokari; Ari Löytynoja; Liina Ahlstén; Jenni Laitila; Carina Wallgren-Pettersson; Katarina Pelin
Journal:  Eur J Hum Genet       Date:  2015-07-22       Impact factor: 4.246

4.  Mutation update: the spectra of nebulin variants and associated myopathies.

Authors:  Vilma-Lotta Lehtokari; Kirsi Kiiski; Sarah A Sandaradura; Jocelyn Laporte; Pauliina Repo; Jennifer A Frey; Kati Donner; Minttu Marttila; Carol Saunders; Peter G Barth; Johan T den Dunnen; Alan H Beggs; Nigel F Clarke; Kathryn N North; Nigel G Laing; Norma B Romero; Thomas L Winder; Katarina Pelin; Carina Wallgren-Pettersson
Journal:  Hum Mutat       Date:  2014-12       Impact factor: 4.878

5.  The complexity of titin splicing pattern in human adult skeletal muscles.

Authors:  Marco Savarese; Per Harald Jonson; Sanna Huovinen; Lars Paulin; Petri Auvinen; Bjarne Udd; Peter Hackman
Journal:  Skelet Muscle       Date:  2018-03-29       Impact factor: 4.912

Review 6.  Nemaline myopathies: a current view.

Authors:  Caroline A Sewry; Jenni M Laitila; Carina Wallgren-Pettersson
Journal:  J Muscle Res Cell Motil       Date:  2019-06-21       Impact factor: 2.698

7.  Role of tropomodulin's leucine rich repeat domain in the formation of neurite-like processes.

Authors:  Laurent Guillaud; Kevin T Gray; Natalia Moroz; Caroline Pantazis; Edward Pate; Alla S Kostyukova
Journal:  Biochemistry       Date:  2014-04-18       Impact factor: 3.162

Review 8.  Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?

Authors:  Marco Savarese; Salla Välipakka; Mridul Johari; Peter Hackman; Bjarne Udd
Journal:  J Neuromuscul Dis       Date:  2020

9.  Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation.

Authors:  Le Thanh Lam; Ian Holt; Jenni Laitila; Mubashir Hanif; Katarina Pelin; Carina Wallgren-Pettersson; Caroline A Sewry; Glenn E Morris
Journal:  Sci Rep       Date:  2018-10-24       Impact factor: 4.379

10.  Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb.

Authors:  Jenni M Laitila; Elyshia L McNamara; Catherine D Wingate; Hayley Goullee; Jacob A Ross; Rhonda L Taylor; Robbert van der Pijl; Lisa M Griffiths; Rachel Harries; Gianina Ravenscroft; Joshua S Clayton; Caroline Sewry; Michael W Lawlor; Coen A C Ottenheijm; Anthony J Bakker; Julien Ochala; Nigel G Laing; Carina Wallgren-Pettersson; Katarina Pelin; Kristen J Nowak
Journal:  Acta Neuropathol Commun       Date:  2020-02-17       Impact factor: 7.801

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