Using complementary DNA from MyoD‐transduced fibroblasts to sequence large muscle genes
Identifieur interne : 006285 ( Main/Exploration ); précédent : 006284; suivant : 006286Using complementary DNA from MyoD‐transduced fibroblasts to sequence large muscle genes
Auteurs : Leigh B. Waddell [Australie] ; Nicole Monnier [France] ; Sandra T. Cooper [Australie] ; Kathryn N. North [Australie] ; Nigel F. Clarke [Australie]Source :
- Muscle & Nerve [ 0148-639X ] ; 2011-08.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Acetylcholine receptor, Achr, Achr antibody concentrations, Arch neurol, Baff, Biopsy, Broblasts, Cdna, Central core disease, Creatine kinase, Crucial role, DNA, Disease manifestation, Frameshift mutation, Further studies, Gdna, Gender distribution, Gravis, Human, Hyperplastic thymus, Messenger RNA, Miguel servet university hospital, Mrna, Mrna decay, Multiple sclerosis, Muscle, Muscle biopsy, Muscle messenger, Muscle mrna, Muscle nerve, Muscle research, Muscular dystrophy, Mutation, Myasthenia, Myasthenia gravis, Myopathy, Nonsense mutation, Nonsense mutations, Ocular, Ocular muscle weakness, Ocular myasthenia gravis, Polymerase chain reaction, Range years, Receptor, Recessive, Roche diagnostics, Ryanodine receptor, Ryr1, Ryr1 allele, Sequencing, Sequencing cdna, Serum concentrations, Serum level, Serum levels, Short reports, Systemic lupus erythematosus, Thymic abnormalities, Type disproportion, Wiley periodicals.
- Teeft :
- Acetylcholine receptor, Achr, Achr antibody concentrations, Arch neurol, Baff, Broblasts, Cdna, Central core disease, Creatine kinase, Crucial role, Disease manifestation, Frameshift mutation, Further studies, Gdna, Gender distribution, Gravis, Hyperplastic thymus, Miguel servet university hospital, Mrna, Mrna decay, Multiple sclerosis, Muscle biopsy, Muscle messenger, Muscle mrna, Muscle nerve, Muscle research, Muscular dystrophy, Mutation, Myasthenia, Myasthenia gravis, Myopathy, Nonsense mutation, Nonsense mutations, Ocular, Ocular muscle weakness, Ocular myasthenia gravis, Polymerase chain reaction, Range years, Receptor, Recessive, Roche diagnostics, Ryr1, Ryr1 allele, Sequencing, Sequencing cdna, Serum concentrations, Serum level, Serum levels, Short reports, Systemic lupus erythematosus, Thymic abnormalities, Type disproportion, Wiley periodicals.
Abstract
Large muscle genes are often sequenced using complementary DNA (cDNA) made from muscle messenger RNA (mRNA) to reduce the cost and workload associated with sequencing from genomic DNA. Two potential barriers are the availability of a frozen muscle biopsy, and difficulties in detecting nonsense mutations due to nonsense‐mediated mRNA decay (NMD). We present patient examples showing that use of MyoD‐transduced fibroblasts as a source of muscle‐specific mRNA overcomes these potential difficulties in sequencing large muscle–related genes. Muscle Nerve, 2011
Url:
DOI: 10.1002/mus.22118
Affiliations:
- Australie, France
- Auvergne-Rhône-Alpes, Nouvelle-Galles du Sud, Rhône-Alpes
- Grenoble, Sydney
- Université de Sydney
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Le document en format XML
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<term>Achr</term>
<term>Achr antibody concentrations</term>
<term>Arch neurol</term>
<term>Baff</term>
<term>Biopsy</term>
<term>Broblasts</term>
<term>Cdna</term>
<term>Central core disease</term>
<term>Creatine kinase</term>
<term>Crucial role</term>
<term>DNA</term>
<term>Disease manifestation</term>
<term>Frameshift mutation</term>
<term>Further studies</term>
<term>Gdna</term>
<term>Gender distribution</term>
<term>Gravis</term>
<term>Human</term>
<term>Hyperplastic thymus</term>
<term>Messenger RNA</term>
<term>Miguel servet university hospital</term>
<term>Mrna</term>
<term>Mrna decay</term>
<term>Multiple sclerosis</term>
<term>Muscle</term>
<term>Muscle biopsy</term>
<term>Muscle messenger</term>
<term>Muscle mrna</term>
<term>Muscle nerve</term>
<term>Muscle research</term>
<term>Muscular dystrophy</term>
<term>Mutation</term>
<term>Myasthenia</term>
<term>Myasthenia gravis</term>
<term>Myopathy</term>
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<term>Ocular muscle weakness</term>
<term>Ocular myasthenia gravis</term>
<term>Polymerase chain reaction</term>
<term>Range years</term>
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<term>Recessive</term>
<term>Roche diagnostics</term>
<term>Ryanodine receptor</term>
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<term>Sequencing</term>
<term>Sequencing cdna</term>
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<term>Serum level</term>
<term>Serum levels</term>
<term>Short reports</term>
<term>Systemic lupus erythematosus</term>
<term>Thymic abnormalities</term>
<term>Type disproportion</term>
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<term>Myasthenia</term>
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<front><div type="abstract" xml:lang="en">Large muscle genes are often sequenced using complementary DNA (cDNA) made from muscle messenger RNA (mRNA) to reduce the cost and workload associated with sequencing from genomic DNA. Two potential barriers are the availability of a frozen muscle biopsy, and difficulties in detecting nonsense mutations due to nonsense‐mediated mRNA decay (NMD). We present patient examples showing that use of MyoD‐transduced fibroblasts as a source of muscle‐specific mRNA overcomes these potential difficulties in sequencing large muscle–related genes. Muscle Nerve, 2011</div>
</front>
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<li>Rhône-Alpes</li>
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<tree><country name="Australie"><region name="Nouvelle-Galles du Sud"><name sortKey="Waddell, Leigh B" sort="Waddell, Leigh B" uniqKey="Waddell L" first="Leigh B." last="Waddell">Leigh B. Waddell</name>
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<name sortKey="Clarke, Nigel F" sort="Clarke, Nigel F" uniqKey="Clarke N" first="Nigel F." last="Clarke">Nigel F. Clarke</name>
<name sortKey="Clarke, Nigel F" sort="Clarke, Nigel F" uniqKey="Clarke N" first="Nigel F." last="Clarke">Nigel F. Clarke</name>
<name sortKey="Clarke, Nigel F" sort="Clarke, Nigel F" uniqKey="Clarke N" first="Nigel F." last="Clarke">Nigel F. Clarke</name>
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