Genetics, Vol. 150, 977-986, November 1998, Copyright © 1998

Sir3p Domains Involved in the Initiation of Telomeric Silencing in Saccharomyces cerevisiae

Yangsuk Parka, John Hanisha, and Arthur J. Lustiga
a Department of Biochemistry, Tulane University Medical Center, New Orleans, Louisiana 70112

Corresponding author: Arthur J. Lustig, Department of Biochemistry, Tulane University Medical Center, 1430 Tulane Ave., New Orleans, LA 70112., alustig{at}mailhost.tcs.tulane.edu (E-mail).

Communicating editor: F. WINSTON

Previous studies from our laboratory have demonstrated that tethering of Sir3p at the subtelomeric/telomeric junction restores silencing in strains containing Rap1-17p, a mutant protein unable to recruit Sir3p. This tethered silencing assay serves as a model system for the early events that follow recruitment of silencing factors, a process we term initiation. A series of LexA fusion proteins in-frame with various Sir3p fragments were constructed and tested for their ability to support tethered silencing. Interestingly, a region comprising only the C-terminal 144 amino acids, termed the C-terminal domain (CTD), is both necessary and sufficient for restoration of silencing. Curiously, the LexA-Sir3N205 mutant protein overcomes the requirement for the CTD, possibly by unmasking a cryptic initiation site. A second domain spanning amino acids 481–835, termed the nonessential for initiation domain (NID), is dispensable for the Sir3p function in initiation, but is required for the recruitment of the Sir4p C terminus. In addition, in the absence of the N-terminal 481 amino acids, the NID negatively influences CTD activity. This suggests the presence of a third region, consisting of the N-terminal half (1–481) of Sir3p, termed the positive regulatory domain (PRD), which is required to initiate silencing in the presence of the NID. These data suggest that the CTD "active" site is under both positive and negative control mediated by multiple Sir3p domains.





This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
H. Liaw and A. J. Lustig
Sir3 C-Terminal Domain Involvement in the Initiation and Spreading of Heterochromatin
Mol. Cell. Biol., October 15, 2006; 26(20): 7616 - 7631.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. A. King, B. E. Hall, M. A. Iwamoto, K. Z. Win, J. F. Chang, and T. Ellenberger
Domain Structure and Protein Interactions of the Silent Information Regulator Sir3 Revealed by Screening a Nested Deletion Library of Protein Fragments
J. Biol. Chem., July 21, 2006; 281(29): 20107 - 20119.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
J. J. Connelly, P. Yuan, H.-C. Hsu, Z. Li, R.-M. Xu, and R. Sternglanz
Structure and Function of the Saccharomyces cerevisiae Sir3 BAH Domain
Mol. Cell. Biol., April 15, 2006; 26(8): 3256 - 3265.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
C.-L. Hsu, Y.-S. Chen, S.-Y. Tsai, P.-J. Tu, M.-J. Wang, and J.-J. Lin
Interaction of Saccharomyces Cdc13p with Pol1p, Imp4p, Sir4p and Zds2p is involved in telomere replication, telomere maintenance and cell growth control
Nucleic Acids Res., January 23, 2004; 32(2): 511 - 521.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
P. Moretti and D. Shore
Multiple Interactions in Sir Protein Recruitment by Rap1p at Silencers and Telomeres in Yeast
Mol. Cell. Biol., December 1, 2001; 21(23): 8082 - 8094.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
E. M. Stone, C. Reifsnyder, M. McVey, B. Gazo, and L. Pillus
Two Classes of sir3 Mutants Enhance the sir1 Mutant Mating Defect and Abolish Telomeric Silencing in Saccharomyces cerevisiae
Genetics, June 1, 2000; 155(2): 509 - 522.
[Abstract] [Full Text]


Home page
GeneticsHome page
S. Enomoto, S. D. Johnston, and J. Berman
Identification of a Novel Allele of SIR3 Defective in the Maintenance, but Not the Establishment, of Silencing in Saccharomyces cerevisiae
Genetics, June 1, 2000; 155(2): 523 - 538.
[Abstract] [Full Text]


Home page
GeneticsHome page
Y. Park and A. J. Lustig
Telomere Structure Regulates the Heritability of Repressed Subtelomeric Chromatin in Saccharomyces cerevisiae
Genetics, February 1, 2000; 154(2): 587 - 598.
[Abstract] [Full Text]