Literature DB >> 15765519

N-RAP expression during mouse heart development.

Shajia Lu1, Diane E Borst, Robert Horowits.   

Abstract

N-RAP gene expression and N-RAP localization were studied during mouse heart development using semiquantitative reverse transcriptase-polymerase chain reaction and immunofluorescence. N-RAP mRNA was detected at embryonic day (E) 10.5, significantly increased from E10.5 to E16.5, and remained essentially constant from E16.5 until 21 days after birth. In E9.5-10.5 heart tissue, N-RAP protein was primarily associated with developing premyofibril structures containing alpha-actinin, as well as with the Z-lines and M-lines of more-mature myofibrils. In contrast, N-cadherin was concentrated in patches at the periphery of the cardiomyocytes. N-RAP labeling markedly increased between E10.5 and E16.5; almost all of the up-regulated N-RAP was associated with intercalated disk structures, and the proportion of mature sarcomeres containing N-RAP decreased. In adult hearts, specific N-RAP staining was only observed at the intercalated disks and was not found in the sarcomeres. The results are consistent with N-RAP functioning as a catalytic scaffolding molecule, with low levels of the scaffold being sufficient to repetitively catalyze key steps in myofibril assembly. Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15765519     DOI: 10.1002/dvdy.20314

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  11 in total

1.  Cardiac-specific NRAP overexpression causes right ventricular dysfunction in mice.

Authors:  Shajia Lu; Garland L Crawford; Justin Dore; Stasia A Anderson; Daryl Despres; Robert Horowits
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2.  Krp1 (Sarcosin) promotes lateral fusion of myofibril assembly intermediates in cultured mouse cardiomyocytes.

Authors:  Cynthia C Greenberg; Patricia S Connelly; Mathew P Daniels; Robert Horowits
Journal:  Exp Cell Res       Date:  2008-03-10       Impact factor: 3.905

3.  Scaffolds and chaperones in myofibril assembly: putting the striations in striated muscle.

Authors:  Garland L Crawford; Robert Horowits
Journal:  Biophys Rev       Date:  2011-03-01

Review 4.  The Nebulin family: an actin support group.

Authors:  Christopher T Pappas; Katherine T Bliss; Anke Zieseniss; Carol C Gregorio
Journal:  Trends Cell Biol       Date:  2010-10-15       Impact factor: 20.808

5.  Myofibril assembly visualized by imaging N-RAP, alpha-actinin, and actin in living cardiomyocytes.

Authors:  Shyam M Manisastry; Kristien J M Zaal; Robert Horowits
Journal:  Exp Cell Res       Date:  2009-02-20       Impact factor: 3.905

6.  Prox1 maintains muscle structure and growth in the developing heart.

Authors:  Catherine A Risebro; Richelle G Searles; Athalie A D Melville; Elisabeth Ehler; Nipurna Jina; Sonia Shah; Jacky Pallas; Mike Hubank; Miriam Dillard; Natasha L Harvey; Robert J Schwartz; Kenneth R Chien; Guillermo Oliver; Paul R Riley
Journal:  Development       Date:  2008-12-17       Impact factor: 6.868

7.  Expression and alternative splicing of N-RAP during mouse skeletal muscle development.

Authors:  Shajia Lu; Diane E Borst; Robert Horowits
Journal:  Cell Motil Cytoskeleton       Date:  2008-12

8.  Role of nonmuscle myosin IIB and N-RAP in cell spreading and myofibril assembly in primary mouse cardiomyocytes.

Authors:  Shajia Lu; Robert Horowits
Journal:  Cell Motil Cytoskeleton       Date:  2008-09

9.  Three-dimensional structure of the intercalated disc reveals plicate domain and gap junction remodeling in heart failure.

Authors:  Christian Pinali; Hayley J Bennett; J Bernard Davenport; Jessica L Caldwell; Tobias Starborg; Andrew W Trafford; Ashraf Kitmitto
Journal:  Biophys J       Date:  2015-02-03       Impact factor: 4.033

10.  Analysis of cardiomyocyte development using immunofluorescence in embryonic mouse heart.

Authors:  Lisa D Wilsbacher; Shaun R Coughlin
Journal:  J Vis Exp       Date:  2015-03-26       Impact factor: 1.355

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