Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (329K) Freely available
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 ISI Web of Science
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 Search for citing articles in:
ISI Web of Science (18)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Xu, M.
Right arrow Articles by Simpson, R. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Xu, M.
Right arrow Articles by Simpson, R. T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, Vol 26, Issue 17 3961-3966, Copyright © 1998 by Oxford University Press


ARTICLES

Cloning, characterization and expression of the gene coding for a cytosine-5-DNA methyltransferase recognizing GpC

M Xu, MP Kladde, JL Van Etten and RT Simpson
Department of Biochemistry and Molecular Biology and the Center for Gene Regulation, 308 Althouse Laboratory,The Pennsylvania State University, University Park, PA 16802-4500, USA.

A novel gene encoding a cytosine-5-DNA methyltransferase recognizing the dinucleotide GpC was cloned from Chlorella virus NYs-1 and expressed in both Escherichia coli and Saccharomyces cerevisiae . The gene was sequenced and a predicted polypeptide of 362 amino acids with a molecular weight of 41.903 kDa was identified. The protein contains several amino acid motifs with high similarity to those of other known 5-methylcytosine-forming methyltransferases. In addition, this enzyme, named M. Cvi PI, shares 66% identity and 76% similarity with M. Cvi JI, the only other cytosine-5-DNA methyltransferase cloned from a Chlorella virus. The short, frequently occurring recognition sequence of the new methyltransferase will be very useful for in vivo chromatin structure studies in both yeast and higher organisms.
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
S.-h. Chan, Z. Zhu, J. L. Van Etten, and S.-y. Xu
Cloning of CviPII nicking and modification system from chlorella virus NYs-1 and application of Nt.CviPII in random DNA amplification
Nucleic Acids Res., November 29, 2004; 32(21): 6187 - 6199.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
C. D. Carvin, R. D. Parr, and M. P. Kladde
Site-selective in vivo targeting of cytosine-5 DNA methylation by zinc-finger proteins
Nucleic Acids Res., November 15, 2003; 31(22): 6493 - 6501.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. D. Carvin, A. Dhasarathy, L. B. Friesenhahn, W. J. Jessen, and M. P. Kladde
Targeted cytosine methylation for in vivo detection of protein-DNA interactions
PNAS, June 24, 2003; 100(13): 7743 - 7748.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
X. Wang and R. T. Simpson
Chromatin structure mapping in Saccharomyces cerevisiae in vivo with DNase I
Nucleic Acids Res., May 1, 2001; 29(9): 1943 - 1950.
[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.