Previous Article | Next Article 
Molecular and Cellular Biology, February 2004, p. 1301-1312, Vol. 24, No. 3
0270-7306/04/$08.00+0 DOI: 10.1128/MCB.24.3.1301-1312.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Nicotinamide Clearance by Pnc1 Directly Regulates Sir2-Mediated Silencing and Longevity
Christopher M. Gallo,
Daniel L. Smith Jr.,
and Jeffrey S. Smith*
Department of Biochemistry and Molecular Genetics, University of Virginia Health System, Charlottesville, Virginia 22908
Received 13 June 2003/
Returned for modification 22 August 2003/
Accepted 30 October 2003
The Saccharomyces cerevisiae Sir2 protein is an NAD+-dependent histone deacetylase (HDAC) that functions in transcriptional silencing and longevity. The NAD+ salvage pathway protein, Npt1, regulates Sir2-mediated processes by maintaining a sufficiently high intracellular NAD+ concentration. However, another NAD+ salvage pathway component, Pnc1, modulates silencing independently of the NAD+ concentration. Nicotinamide (NAM) is a by-product of the Sir2 deacetylase reaction and is a natural Sir2 inhibitor. Pnc1 is a nicotinamidase that converts NAM to nicotinic acid. Here we show that recombinant Pnc1 stimulates Sir2 HDAC activity in vitro by preventing the accumulation of NAM produced by Sir2. In vivo, telomeric, rDNA, and HM silencing are differentially sensitive to inhibition by NAM. Furthermore, PNC1 overexpression suppresses the inhibitory effect of exogenously added NAM on silencing, life span, and Hst1-mediated transcriptional repression. Finally, we show that stress suppresses the inhibitory effect of NAM through the induction of PNC1 expression. Pnc1, therefore, positively regulates Sir2-mediated silencing and longevity by preventing the accumulation of intracellular NAM during times of stress.
* Corresponding author. Mailing address: University of Virginia Health System, Department of Biochemistry and Molecular Genetics, Jordan Hall, Box 800733, Charlottesville, VA 22908. Phone: (434) 243-5864. Fax: (434) 924-5069. E-mail:
jss5y{at}virginia.edu.
C.M.G. and D.L.S. contributed equally to the work.
Molecular and Cellular Biology, February 2004, p. 1301-1312, Vol. 24, No. 3
0022-538X/04/$08.00+0 DOI: 10.1128/MCB.24.3.1301-1312.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Vrablik, T. L., Huang, L., Lange, S. E., Hanna-Rose, W.
(2009). Nicotinamidase modulation of NAD+ biosynthesis and nicotinamide levels separately affect reproductive development and cell survival in C. elegans. Development
136: 3637-3646
[Abstract]
[Full Text]
-
Zhou, J., Zhong, Q., Li, G., Greenberg, M. L.
(2009). Loss of Cardiolipin Leads to Longevity Defects That Are Alleviated by Alterations in Stress Response Signaling. J. Biol. Chem.
284: 18106-18114
[Abstract]
[Full Text]
-
Balan, V., Miller, G. S., Kaplun, L., Balan, K., Chong, Z.-Z., Li, F., Kaplun, A., VanBerkum, M. F. A., Arking, R., Freeman, D. C., Maiese, K., Tzivion, G.
(2008). Life Span Extension and Neuronal Cell Protection by Drosophila Nicotinamidase. J. Biol. Chem.
283: 27810-27819
[Abstract]
[Full Text]
-
McClure, J. M., Gallo, C. M., Smith, D. L. Jr., Matecic, M., Hontz, R. D., Buck, S. W., Racette, F. G., Smith, J. S.
(2008). Pnc1p-Mediated Nicotinamide Clearance Modifies the Epigenetic Properties of rDNA Silencing in Saccharomyces cerevisiae. Genetics
180: 797-810
[Abstract]
[Full Text]
-
Easlon, E., Tsang, F., Skinner, C., Wang, C., Lin, S.-J.
(2008). The malate-aspartate NADH shuttle components are novel metabolic longevity regulators required for calorie restriction-mediated life span extension in yeast. Genes Dev.
22: 931-944
[Abstract]
[Full Text]
-
Sauve, A. A.
(2008). NAD+ and Vitamin B3: From Metabolism to Therapies. J. Pharmacol. Exp. Ther.
324: 883-893
[Abstract]
[Full Text]
-
Easlon, E., Tsang, F., Dilova, I., Wang, C., Lu, S.-P., Skinner, C., Lin, S.-J.
(2007). The Dihydrolipoamide Acetyltransferase Is a Novel Metabolic Longevity Factor and Is Required for Calorie Restriction-mediated Life Span Extension. J. Biol. Chem.
282: 6161-6171
[Abstract]
[Full Text]
-
Khan, A. N., Lewis, P. N.
(2006). Use of Substrate Analogs and Mutagenesis to Study Substrate Binding and Catalysis in the Sir2 Family of NAD-dependent Protein Deacetylases. J. Biol. Chem.
281: 11702-11711
[Abstract]
[Full Text]
-
Lamming, D. W., Latorre-Esteves, M., Medvedik, O., Wong, S. N., Tsang, F. A., Wang, C., Lin, S.-J., Sinclair, D. A.
(2005). HST2 Mediates SIR2-Independent Life-Span Extension by Calorie Restriction. Science
309: 1861-1864
[Abstract]
[Full Text]
-
Michel, A. H., Kornmann, B., Dubrana, K., Shore, D.
(2005). Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing. Genes Dev.
19: 1199-1210
[Abstract]
[Full Text]
-
Xu, J., Capezzone, M., Xu, X., Hershman, J. M.
(2005). Activation of Nicotinamide N-Methyltransferase Gene Promoter by Hepatocyte Nuclear Factor-1{beta} in Human Papillary Thyroid Cancer Cells. Mol. Endocrinol.
19: 527-539
[Abstract]
[Full Text]
-
Revollo, J. R., Grimm, A. A., Imai, S.-i.
(2004). The NAD Biosynthesis Pathway Mediated by Nicotinamide Phosphoribosyltransferase Regulates Sir2 Activity in Mammalian Cells. J. Biol. Chem.
279: 50754-50763
[Abstract]
[Full Text]
-
Tanny, J. C., Kirkpatrick, D. S., Gerber, S. A., Gygi, S. P., Moazed, D.
(2004). Budding Yeast Silencing Complexes and Regulation of Sir2 Activity by Protein-Protein Interactions. Mol. Cell. Biol.
24: 6931-6946
[Abstract]
[Full Text]
-
Zhao, K., Harshaw, R., Chai, X., Marmorstein, R.
(2004). Structural basis for nicotinamide cleavage and ADP-ribose transfer by NAD+-dependent Sir2 histone/protein deacetylases. Proc. Natl. Acad. Sci. USA
101: 8563-8568
[Abstract]
[Full Text]
-
Buck, S. W., Gallo, C. M., Smith, J. S.
(2004). Diversity in the Sir2 family of protein deacetylases. J. Leukoc. Biol.
75: 939-950
[Abstract]
[Full Text]