Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2006-4-6
pubmed:abstractText
The HSL7 (histone synthetic lethal 7) gene in the yeast Saccharomyces cerevisiae encodes a protein with close sequence similarity to the mammalian PRMT5 protein, a member of the class of protein arginine methyltransferases that catalyses the formation of omega-N(G)-monomethylarginine and symmetric omega-N(G),N'(G)-dimethylarginine residues in a number of methyl-accepting species. A full-length HSL7 construct was expressed as a FLAG-tagged protein in Saccharomyces cerevisiae. We found that FLAG-tagged Hsl7 effectively catalyses the transfer of methyl groups from S-adenosyl-[methyl-3H]-L-methionine to calf thymus histone H2A. When the acid-hydrolysed radiolabelled protein products were separated by high-resolution cation-exchange chromatography, we were able to detect one tritiated species that co-migrated with an omega-N(G)-monomethylarginine standard. No radioactivity was observed that co-migrated with either the asymmetric or symmetric dimethylated derivatives. In control experiments, no methylation of histone H2A was found with two mutant constructs of Hsl7. Surprisingly, FLAG-Hsl7 does not appear to effectively catalyse the in vitro methylation of a GST (glutathione S-transferase)-GAR [glycine- and arginine-rich human fibrillarin-(1-148) peptide] fusion protein or bovine brain myelin basic protein, both good methyl-accepting substrates for the human homologue PRMT5. Additionally, FLAG-Hsl7 demonstrates no activity on purified calf thymus histones H1, H2B, H3 or H4. GST-Rmt1, the GST-fusion protein of the major yeast protein arginine methyltransferase, was also found to methylate calf thymus histone H2A. Although we detected Rmt1-dependent arginine methylation in vivo in purified yeast histones H2A, H2B, H3 and H4, we found no evidence for Hsl7-dependent methylation of endogenous yeast histones. The physiological substrates of the Hsl7 enzyme remain to be identified.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10381882, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10411908, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10490630, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10531356, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10652296, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10749851, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10903903, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-10931850, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-11408575, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-11413150, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-11713266, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-11856739, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-12101096, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-12171910, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-12756295, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-15025441, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-15866169, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-8647431, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-8647869, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-8675010, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-8675011, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-9499403, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-9642256, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-9752719, http://linkedlifedata.com/resource/pubmed/commentcorrection/16426232-9873020
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1470-8728
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
395
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
563-70
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:16426232-Amino Acid Sequence, pubmed-meshheading:16426232-Animals, pubmed-meshheading:16426232-Catalysis, pubmed-meshheading:16426232-Cattle, pubmed-meshheading:16426232-Gene Expression, pubmed-meshheading:16426232-Histones, pubmed-meshheading:16426232-Methylation, pubmed-meshheading:16426232-Methyltransferases, pubmed-meshheading:16426232-Molecular Sequence Data, pubmed-meshheading:16426232-Protein Kinases, pubmed-meshheading:16426232-Protein-Arginine N-Methyltransferases, pubmed-meshheading:16426232-Saccharomyces cerevisiae, pubmed-meshheading:16426232-Saccharomyces cerevisiae Proteins, pubmed-meshheading:16426232-Sequence Alignment, pubmed-meshheading:16426232-Substrate Specificity, pubmed-meshheading:16426232-Thymus Gland, pubmed-meshheading:16426232-omega-N-Methylarginine
pubmed:year
2006
pubmed:articleTitle
Yeast Hsl7 (histone synthetic lethal 7) catalyses the in vitro formation of omega-N(G)-monomethylarginine in calf thymus histone H2A.
pubmed:affiliation
The Department of Chemistry and Biochemistry and the Molecular Biology Institute, UCLA (University of California, Los Angeles), Los Angeles, CA 90095-1569, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural