Structural and functional characteristics of two sodium-coupled dicarboxylate transporters (ceNaDC1 and ceNaDC2) from Caenorhabditis elegans and their relevance to life span
- PMID: 12480943
- DOI: 10.1074/jbc.M208763200
Structural and functional characteristics of two sodium-coupled dicarboxylate transporters (ceNaDC1 and ceNaDC2) from Caenorhabditis elegans and their relevance to life span
Abstract
We have cloned and functionally characterized two Na(+)-coupled dicarboxylate transporters, namely ceNaDC1 and ceNaDC2, from Caenorhabditis elegans. These two transporters show significant sequence homology with the product of the Indy gene identified in Drosophila melanogaster and with the Na(+)-coupled dicarboxylate transporters NaDC1 and NaDC3 identified in mammals. In a mammalian cell heterologous expression system, the cloned ceNaDC1 and ceNaDC2 mediate Na(+)-coupled transport of various dicarboxylates. With succinate as the substrate, ceNaDC1 exhibits much lower affinity compared with ceNaDC2. Thus, ceNaDC1 and ceNaDC2 correspond at the functional level to the mammalian NaDC1 and NaDC3, respectively. The nadc1 and nadc2 genes are not expressed at the embryonic stage, but the expression is detectable all through the early larva stage to the adult stage. Tissue-specific expression pattern studies using a reporter gene fusion approach in transgenic C. elegans show that both genes are coexpressed in the intestinal tract, an organ responsible for not only the digestion and absorption of nutrients but also for the storage of energy in this organism. Independent knockdown of the function of these two transporters in C. elegans using the strategy of RNA interference suggests that NaDC1 is not associated with the regulation of average life span in this organism, whereas the knockdown of NaDC2 function leads to a significant increase in the average life span. Disruption of the function of the high affinity Na(+)-coupled dicarboxylate transporter NaDC2 in C. elegans may lead to decreased availability of dicarboxylates for cellular production of metabolic energy, thus creating a biological state similar to that of caloric restriction, and consequently leading to life span extension.
Similar articles
-
Relevance of NAC-2, an Na+-coupled citrate transporter, to life span, body size and fat content in Caenorhabditis elegans.Biochem J. 2004 Apr 1;379(Pt 1):191-8. doi: 10.1042/BJ20031807. Biochem J. 2004. PMID: 14678010 Free PMC article.
-
Functional identity of Drosophila melanogaster Indy as a cation-independent, electroneutral transporter for tricarboxylic acid-cycle intermediates.Biochem J. 2002 Oct 15;367(Pt 2):313-9. doi: 10.1042/BJ20021132. Biochem J. 2002. PMID: 12186628 Free PMC article.
-
Threonine-509 is a determinant of apparent affinity for both substrate and cations in the human Na+/dicarboxylate cotransporter.Biochemistry. 2008 Jan 22;47(3):1087-93. doi: 10.1021/bi701417h. Epub 2007 Dec 28. Biochemistry. 2008. PMID: 18161988 Free PMC article.
-
Sodium-coupled transporters for Krebs cycle intermediates.Annu Rev Physiol. 1999;61:663-82. doi: 10.1146/annurev.physiol.61.1.663. Annu Rev Physiol. 1999. PMID: 10099705 Review.
-
Sodium-coupled dicarboxylate and citrate transporters from the SLC13 family.Pflugers Arch. 2014 Jan;466(1):119-30. doi: 10.1007/s00424-013-1369-y. Epub 2013 Oct 10. Pflugers Arch. 2014. PMID: 24114175 Review.
Cited by
-
Targeting metabolic pathways for extension of lifespan and healthspan across multiple species.Ageing Res Rev. 2020 Dec;64:101188. doi: 10.1016/j.arr.2020.101188. Epub 2020 Oct 5. Ageing Res Rev. 2020. PMID: 33031925 Free PMC article. Review.
-
High-affinity Na(+)-dependent dicarboxylate cotransporter promotes cellular senescence by inhibiting SIRT1.Mech Ageing Dev. 2010 Oct;131(10):601-13. doi: 10.1016/j.mad.2010.08.006. Epub 2010 Sep 9. Mech Ageing Dev. 2010. PMID: 20813124 Free PMC article.
-
Identification of transport pathways for citric acid cycle intermediates in the human colon carcinoma cell line, Caco-2.Biochim Biophys Acta. 2008 Apr;1778(4):1051-9. doi: 10.1016/j.bbamem.2007.12.013. Epub 2007 Dec 23. Biochim Biophys Acta. 2008. PMID: 18194662 Free PMC article.
-
Inhibition of citrate cotransporter Slc13a5/mINDY by RNAi improves hepatic insulin sensitivity and prevents diet-induced non-alcoholic fatty liver disease in mice.Mol Metab. 2016 Aug 13;5(11):1072-1082. doi: 10.1016/j.molmet.2016.08.004. eCollection 2016 Nov. Mol Metab. 2016. PMID: 27818933 Free PMC article.
-
Ala-504 is a determinant of substrate binding affinity in the mouse Na(+)/dicarboxylate cotransporter.Biochim Biophys Acta. 2006 Jun;1758(6):781-8. doi: 10.1016/j.bbamem.2006.05.005. Epub 2006 May 16. Biochim Biophys Acta. 2006. PMID: 16787639 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases