Skip Navigation

This Article
Right arrow Print PDF (655K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Sancar, G. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sancar, G. B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1985, Vol. 13, No. 22 8231-8246
© 1985


Articles

Sequence of the Saccharomyces cerevisiae PHRI gene and homology of the PHRI photolyase to E. coli photolyase

Gwendolyn B. Sancar

Department of Biochemistry 231H, University of North Carolina, Chapel Hill, NC 27514, USA

Received August 12, 1985. Revised October 24, 1985. Accepted October 24, 1985.

The nucleotide sequence of a 2301 base pair region of Saccharomyces carevisiae DNA containing the PHRI gene is reported. Within this region a single open reading frame of 1695 base pairs was found; using the insertional inactivation technique it was shown that part or all of this open reading frame specifies the PHRI-encoded photolyase. The amino acid sequence of the 565 amino acid long polypeptide predicted from the PHRI nucleotide sequence was compared to the amino acid sequence of E. coli photolyase. Overall the sequence homology was 36.5%; however, two short regions near the amino terminus as well as the carboxy-terminal 150 amino acids display significantly greater sequence homology. The presence of these strongly conserved regions suggests that the yeast and E. coli photolyase possess common structural and functional domains involved in substrate and/or chromophore binding.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
Y. Zhu and W. Xiao
Pdr3 is required for DNA damage induction of MAG1 and DDI1 via a bi-directional promoter element
Nucleic Acids Res., September 27, 2004; 32(17): 5066 - 5075.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
B. Suter, R.-E. Wellinger, and F. Thoma
DNA repair in a yeast origin of replication: contributions of photolyase and nucleotide excision repair
Nucleic Acids Res., May 15, 2000; 28(10): 2060 - 2068.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
Y. K. Jang, L. Wang, and G. B. Sancar
RPH1 and GIS1 Are Damage-Responsive Repressors of PHR1
Mol. Cell. Biol., November 1, 1999; 19(11): 7630 - 7638.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
G. Berrocal-Tito, L. Sametz-Baron, K. Eichenberg, B. A. Horwitz, and A. Herrera-Estrella
Rapid Blue Light Regulation of a Trichoderma harzianum Photolyase Gene
J. Biol. Chem., May 14, 1999; 274(20): 14288 - 14294.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
S. Meeusen, Q. Tieu, E. Wong, E. Weiss, D. Schieltz, J. R. Yates, and J. Nunnari
Mgm101p Is a Novel Component of the Mitochondrial Nucleoid That Binds DNA and Is Required for the Repair of Oxidatively Damaged Mitochondrial DNA
J. Cell Biol., April 19, 1999; 145(2): 291 - 304.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
B. J. Vande Berg and G. B. Sancar
Evidence for Dinucleotide Flipping by DNA Photolyase
J. Biol. Chem., August 7, 1998; 273(32): 20276 - 20284.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. S. Branda and G. Isaya
Prediction and Identification of New Natural Substrates of the Yeast Mitochondrial Intermediate Peptidase
J. Biol. Chem., November 10, 1995; 270(45): 27366 - 27373.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.