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Using complementary DNA from MyoD‐transduced fibroblasts to sequence large muscle genes

Identifieur interne : 006285 ( Main/Exploration ); précédent : 006284; suivant : 006286

Using 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 :

RBID : ISTEX:4ECFDC93BF3F4DDD5AFFFDD940151AEE62BC714E

Descripteurs français

English descriptors

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:


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Le document en format XML

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<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>
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