Effect of nonsense-mediated mRNA decay factor SMG9 deficiency on premature aging in zebrafish
SMG9 is an essential component of the nonsense-mediated mRNA decay (NMD) machinery, a quality control mechanism that selectively degrades aberrant transcripts. Mutations in SMG9 are associated with heart and brain malformation syndrome (HBMS). However, the molecular mechanism underlying HBMS remains...
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Published in | Communications biology Vol. 7; no. 1; p. 654 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
28.05.2024
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | SMG9 is an essential component of the nonsense-mediated mRNA decay (NMD) machinery, a quality control mechanism that selectively degrades aberrant transcripts. Mutations in SMG9 are associated with heart and brain malformation syndrome (HBMS). However, the molecular mechanism underlying HBMS remains unclear. We generated
smg9
mutant zebrafish (
smg9
oi7/oi7
) that have a lifespan of approximately 6 months or longer, allowing for analysis of the in vivo function of Smg9 in adults in more detail.
smg9
oi7/oi7
zebrafish display congenital brain abnormalities and reduced cardiac contraction. Additionally,
smg9
oi7/oi7
zebrafish exhibit a premature aging phenotype. Analysis of NMD target mRNAs shows a trend toward increased mRNA levels in
smg9
oi7/oi7
zebrafish. Spermidine oxidase (Smox) is increased in
smg9
oi7/oi7
zebrafish, resulting in the accumulation of byproducts, reactive oxygen species, and acrolein. The accumulation of
smox
mRNA due to NMD dysregulation caused by Smg9 deficiency leads to increased oxidative stress, resulting in premature aging.
SMG9 deficiency in zebrafish leads to brain abnormalities, cardiac dysfunction, and premature aging due to disrupted nonsense-mediated mRNA decay and increased oxidative stress caused by elevated spermidine oxidase (Smox) levels. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2399-3642 2399-3642 |
DOI: | 10.1038/s42003-024-06356-6 |