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Target Concepts:
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Query: UMLS:C0023380 (
lethargy
)
5,697
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
A spontaneously arising, loss-of-function mutation in the RNA binding motif protein 20 (
Rbm20
) gene, which encodes a nuclear splicing protein, was previously identified as the underlying reason for expression of an abnormally large TITIN (TTN) protein in a rat model of cardiomyopathy. An outbreak of
Pseudomonas aeruginosa
led to submission of rats with dyspnea, sneezing,
lethargy
, nasal discharge, and/or unexpected death for diagnostic evaluation. Necropsy revealed underlying megaesophagus in
Rbm20
-/-
rats. Further phenotyping of this rat strain and determination of the size of esophageal TTN was undertaken. The
Rbm20
-defective rats developed megaesophagus at an early age (26 weeks) with high frequency (13/32, 41%). They also often exhibited secondary rhinitis (9/32, 28%), aspiration pneumonia (8/32, 25%), and otitis media/interna (6/32, 19%). In addition, these rats had a high prevalence of hydronephrosis (13/32, 41%). RBM20 is involved in splicing multiple RNA transcripts, one of which is the
muscle-specific protein
TTN.
Rbm20
mutations are a significant cause of dilated cardiomyopathy in humans. In
Rbm20
-defective rats, TTN size was significantly increased in the skeletal muscle of the esophagus. Megaesophagus in this rat strain (maintained on a mixed genetic background) is hypothesized to result from altered TTN stretch signaling in esophageal skeletal muscle. This study describes a novel mechanism for the development of megaesophagus, which may be useful for understanding the pathogenesis of megaesophagus in humans and offers insights into potential myogenic causes of this condition. This is the first report of megaesophagus and other noncardiac pathogenic changes associated with mutation of
Rbm20
in any species.
...
PMID:Megaesophagus Is a Major Pathological Condition in Rats With a Large Deletion in the
Rbm20
Gene. 3122 Oct 19