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Journal of Biomedical Science
Article . 2008 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
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Letter to the Editor: Overexpression of Myostatin2 in zebrafish reduces the expression of dystrophin associated protein complex (DAPC) which leads to muscle dystrophy

Authors: Buel D, Rodgers;

Letter to the Editor: Overexpression of Myostatin2 in zebrafish reduces the expression of dystrophin associated protein complex (DAPC) which leads to muscle dystrophy

Abstract

I recently read “Overexpression of Myostatin2 in zebrafish reduces the expression of dystrophin associated protein complex (DAPC) which leads to muscle dystrophy” (Amali et al. Epub, May 6) with great interest, but also with some concern. The authors claim to have cloned for the first time a second myostatin homolog in zebrafish and partially characterized its function. However, the cDNA and genomic clones for this gene were reported in 2005 by two different research groups, including our own [1, 2], although these studies were not referenced by Amali et al. These sequences have also been publicly available since this time and are accessible from GenBank. In fact, all of the data presented in the first three figures of Amali et al. were formerly presented in part or, in some instances, in much greater detail. Readers should be made aware of this oversight for two very important reasons. Firstly, the gene nomenclature used by Amali et al. is incorrect as the entire subfamily’s nomenclature was revised last year [3]. Many of the fish gene names did not match the previously determined phylogenies [2, 4, 5] and as such, the revised nomenclature was accepted by the Mouse Genomic Nomenclature Committee and the Human Genome Organization (HUGO) Gene Nomenclature Committee, which subsequently revised their databases. This change was also propagated to other public databases including those managed by the National Center for Biotechnology Information (NCBI) and Ensemble. The old and misleading nomenclature that misidentifies myostatin (MSTN)-1 with MSTN-2 (and vice versa) was used by Amali et al., further confuses the field and needs to be corrected. In fact, the phylogenetic analysis by Amali et al. includes several genes that are “misplaced” in the wrong clade, although this was not recognized by the authors. Secondly, and probably most importantly, appropriate credit and future references should be directed to the young scientists whose career advancements depend upon the recognition of their hard work [1, 2]. Amali et al. present some intriguing and novel data that are worthy of attention. However, identification of the second paralogous myostatin gene family as well as the characterization of the zebrafish clones was accomplished by Kerr et al. and Biga et al. in 2005 and not by Amali et al. in 2008.

Related Organizations
Keywords

Molecular Sequence Data, Animals, Amino Acid Sequence, Muscular Dystrophy, Animal, Myostatin, Zebrafish Proteins, Sequence Alignment, Phylogeny, Zebrafish, Dystrophin-Associated Protein Complex

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
1
Average
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