Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0004104
DC Field | Value | |
---|---|---|
dc.title | Nematode homologue of PQBP1, a mental retardation causative gene, is involved in lipid metabolism | |
dc.contributor.author | Takahashi K. | |
dc.contributor.author | Yoshina S. | |
dc.contributor.author | Masashi M. | |
dc.contributor.author | Ito W. | |
dc.contributor.author | Inoue T. | |
dc.contributor.author | Shiwaku H. | |
dc.contributor.author | Arai H. | |
dc.contributor.author | Mitani S. | |
dc.contributor.author | Okazawa H. | |
dc.date.accessioned | 2019-11-08T00:54:35Z | |
dc.date.available | 2019-11-08T00:54:35Z | |
dc.date.issued | 2009 | |
dc.identifier.citation | Takahashi K., Yoshina S., Masashi M., Ito W., Inoue T., Shiwaku H., Arai H., Mitani S., Okazawa H. (2009). Nematode homologue of PQBP1, a mental retardation causative gene, is involved in lipid metabolism. PLoS ONE 4 (1) : e4104. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0004104 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/161845 | |
dc.description.abstract | Background: PQBP1 is a causative gene for X-linked mental retardation (MR) whose patients frequently show lean body. C. elegans has a strictly conserved homologue gene of PQBP1, T21D12.3. Methodology and Principal Findings: We generated Venus-transgenic and T21D12.3-mutant nematodes to analyze developmental expression patterns and in vivo functions of the nematode PQBP1 homologue protein (pqbp-1.1). During development, pqbp-1.1 is expressed from cell proliferation stage to larva stage. In larva, intestinal cells show the highest expression of pqbp-1.1, while it decreases in adult worms. The mutants of pqbp-1.1 show a decrease of the lipid content in intestinal cells. Especially, incorporation of fatty acid into triglyceride is impaired. ShRNA-mediated repression of PQBP1 also leads to reduction of lipid content in mammalian primary white adipocytes. Conclusion/Significance: These results suggest that pqbp-1.1 is involved in lipid metabolism of intestinal cells. Dysfunction of lipid metabolism might underlie lean body, one of the most frequent symptoms associating with PQBP1-linked MR patients. � 2009 Takahashi et al. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20191101 | |
dc.subject | binding protein | |
dc.subject | fatty acid | |
dc.subject | polyglutamate binding protein | |
dc.subject | protein PQBP1 | |
dc.subject | short hairpin RNA | |
dc.subject | triacylglycerol | |
dc.subject | unclassified drug | |
dc.subject | Caenorhabditis elegans protein | |
dc.subject | carrier protein | |
dc.subject | hybrid protein | |
dc.subject | nuclear protein | |
dc.subject | PQBP1 protein, human | |
dc.subject | adipocyte | |
dc.subject | article | |
dc.subject | Caenorhabditis elegans | |
dc.subject | cell proliferation | |
dc.subject | controlled study | |
dc.subject | evolutionary homology | |
dc.subject | gene expression | |
dc.subject | gene function | |
dc.subject | gene repression | |
dc.subject | in vivo study | |
dc.subject | intestine cell | |
dc.subject | larval stage | |
dc.subject | lipid analysis | |
dc.subject | lipid metabolism | |
dc.subject | mutant | |
dc.subject | nonhuman | |
dc.subject | protein defect | |
dc.subject | protein function | |
dc.subject | transgenics | |
dc.subject | animal | |
dc.subject | Caenorhabditis elegans | |
dc.subject | cell culture | |
dc.subject | cytology | |
dc.subject | genetics | |
dc.subject | histology | |
dc.subject | human | |
dc.subject | intestine | |
dc.subject | metabolism | |
dc.subject | physiology | |
dc.subject | syndrome | |
dc.subject | transgenic animal | |
dc.subject | white adipose tissue | |
dc.subject | X linked mental retardation | |
dc.subject | Caenorhabditis elegans | |
dc.subject | Mammalia | |
dc.subject | Nematoda | |
dc.subject | Adipocytes | |
dc.subject | Adipose Tissue, White | |
dc.subject | Animals | |
dc.subject | Animals, Genetically Modified | |
dc.subject | Caenorhabditis elegans | |
dc.subject | Caenorhabditis elegans Proteins | |
dc.subject | Carrier Proteins | |
dc.subject | Cells, Cultured | |
dc.subject | Humans | |
dc.subject | Intestines | |
dc.subject | Lipid Metabolism | |
dc.subject | Mental Retardation, X-Linked | |
dc.subject | Nuclear Proteins | |
dc.subject | Recombinant Fusion Proteins | |
dc.subject | Syndrome | |
dc.type | Article | |
dc.contributor.department | BIOCHEMISTRY | |
dc.description.doi | 10.1371/journal.pone.0004104 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 4 | |
dc.description.issue | 1 | |
dc.description.page | e4104 | |
Appears in Collections: | Staff Publications Elements |
Show simple item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_1371_journal_pone_0004104.pdf | 450.42 kB | Adobe PDF | OPEN | None | View/Download |
This item is licensed under a Creative Commons License