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Rapid Muscle Relaxation in Siniperca chuatsi is Coordinated by Parvalbumin (PVALB) and MiR-181a
- Source :
- Current Molecular Medicine. 15:772-779
- Publication Year :
- 2015
- Publisher :
- Bentham Science Publishers Ltd., 2015.
-
Abstract
- Parvalbumins (PVALBs) are particularly abundant in the fast-contracting muscles and correlate positively with muscle relaxation speed in amphibians and fishes. MiRNAs play important roles in diverse biologic processes via binding to the 3’ untranslated region (3’UTR) of the target mRNAs. In the study, four PVALB isoforms, named as PVALB1, 2, 3, and 4, were identified in the mandarin fish ( Siniperca chuatsi ) fast muscle and PVALB4 exhibited the highest expression level among them. By bioinformatics analysis, a putative miR-181a binding site in PVALB4 was detected and the direct interaction between miR-181a and PVALB4 was confirmed with the luciferase reporter assay. Further, when miR-181a was inhibited, it substantially increased PVALB4 mRNA expression level and the muscle relaxation rate in vivo . Taken together, the obtained results suggest that miRNA-181a/PVALB4 is an evolutionarily conserved miRNAtarget pair and their interaction is correlated with muscle relaxation rate in the mandarin fish. Therefore, the study revealed a novel molecular mechanism in the regulation of skeletal muscle relaxation in fish.
- Subjects :
- Untranslated region
Gene isoform
Muscle Relaxation
Parvalbumins
Molecular Sequence Data
Gene Expression
Biochemistry
Siniperca chuatsi
medicine
Animals
Humans
Amino Acid Sequence
RNA, Messenger
Cloning, Molecular
Binding site
3' Untranslated Regions
Molecular Biology
Phylogeny
Binding Sites
Base Sequence
biology
Fishes
Skeletal muscle
Sequence Analysis, DNA
General Medicine
biology.organism_classification
Molecular biology
MicroRNAs
Muscle relaxation
medicine.anatomical_structure
Multigene Family
biology.protein
Molecular Medicine
RNA Interference
Sequence Alignment
Parvalbumin
Subjects
Details
- ISSN :
- 15665240
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Current Molecular Medicine
- Accession number :
- edsair.doi.dedup.....5d9c257a0d4be70570eb3afb0f668c19
- Full Text :
- https://doi.org/10.2174/1566524015666150921110037